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Teresa Coelho. Licenciatura em Medicina pela Faculdade de CIências Médicas da Universidade Nova de LIsboa, em 1980. Completou a especialidade de Neurologia em 1990 e o Ciclo de Estudos Especiais de Neurofisiologia Clínica em 1994. Doutoramento em Ciências Médicas pelo Instituto de Ciências Biomédicas da Univerisdade do Porto, em 2019. Assitente Graduada Sénior de Neurofisiologia do Centro Hospitalar Universitário do Porto desde 2018, onde desempenha funções de Responsável da Consulta de Neurologia/Doenças Neuromuculares, de Responsável da Unidade Corino de Andrade, Centro de Referência Nacional para a Paramiloidose Familiar e de Diretora do Serviço de Neurofisiologia. O seu trabalho clínico e de investigação clínica e translacional concentra-se em três áreas principais: a amiloidose por transtirretina, com ênfase na descrição clínica da doença, na compreensão dos mecanismos patogénicos, no diagnóstico precoce e na avaliação da progressão da doença e no desenvolvimento de tratamentos modificadores da doença; as doenças neuromusculares hereditárias com particular atenção à sua descrição clínica, ao diagnóstico genético e ao impacto dos tratamentos modificadores da doença; a neurofisiologia clínica na vertente do estudo do Sistema Nervoso Periférico, através do estudo da condução nervosa, da eletromiografia e de técnicas de estudo das pequenas fibras nervosas. É autora e co-autora de mais de 100 artigos publicados em revistas internacionais. Participa/ou como investigadora principal ou co-investigadora em projetos de investigação clínica, incluindo inúmeros ensaios clínicos, e translacional, nacionais e internacionais. Foi investigadora principal e coordenadora nacional dos ensaios clínicos que conduziram à aprovação de 3 medicamentos modificadores da doença para o tratamento da polineuropatia da amiloidose por transtirretina.
Identificação

Identificação pessoal

Nome completo
Teresa Coelho
Data de nascimento
1956/10/08
Género
Feminino

Nomes de citação

  • Coelho, Teresa
  • Teresa Coelho

Identificadores de autor

Ciência ID
C71E-3343-F445

Telefones

Telefone
  • 222077500 Ext.: 1486 (Profissional)

Moradas

  • Centro Hospitalar do Porto - Hospital Santo António. Largo Abel Salazar, 4099-001, Porto, Porto, Portugal (Profissional)

Domínios de atuação

  • Ciências Médicas e da Saúde - Medicina Clínica - Neurologia Clínica
  • Ciências Médicas e da Saúde
  • Ciências Médicas e da Saúde - Medicina Básica - Neurociências
  • Ciências Médicas e da Saúde - Medicina Básica - Genética Humana

Idiomas

Idioma Conversação Leitura Escrita Compreensão Peer-review
Inglês Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1)
Francês Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1)
Espanhol; Castelhano Utilizador independente (B1) Utilizador independente (B2) Utilizador elementar (A2) Utilizador independente (B2) Utilizador elementar (A2)
Português (Idioma materno)
Formação
Grau Classificação
2019/07/15
Concluído
Ciências Médicas (Doutoramento)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
"Disease modifying therapies for attr amyloidoses: clinical development of new drugs and impact on the natural history of the disease" (TESE/DISSERTAÇÃO)
Aprovado
2018
Concluído
Neurophysiology Senior Graduate Degree (Outros)
Centro Hospitalar Universitário do Porto EPE, Portugal
2009/05/01
Concluído
Brachial Plexus Assessment. (Postgraduate Certificate)
American Academy of Neurology, Estados Unidos
2009/05/01
Concluído
New Genetics: The Future Of Neurology. (Postgraduate Certificate)
American Academy of Neurology, Estados Unidos
2009/04/27
Concluído
Autoimmune Antibody Testing In Neuropathy: Indications For Practicing Neurologist. (Postgraduate Certificate)
American Academy of Neurology, Estados Unidos
2009/04/27
Concluído
Neuromuscular Therapy. (Postgraduate Certificate)
American Academy of Neurology, Estados Unidos
1997
Concluído
Neurophysiology Graduate Degree (Outros)
Centro Hospitalar Universitário do Porto EPE, Portugal
1994
Concluído
Neurophysiology Training at the Department of Neurophysiology (Especialização pós-licenciatura)
Centro Hospitalar Universitário do Porto EPE, Portugal
1993/03
Concluído
Internship at the Autonomic Nervous System Studies Laboratory at the Department of Neurophysiology. (Postgraduate Certificate)
Hospital Universitario La Paz, Espanha
1990
Concluído
Specialist in Neurology (Título de especialista)
Centro Hospitalar Universitário do Porto EPE, Portugal
1984
Concluído
Voluntary Residency in Intesive Care Unit (Outros)
Centro Hospitalar Universitário do Porto EPE, Portugal
1980
Concluído
Medicine (Licenciatura)
Universidade de Lisboa Faculdade de Medicina, Portugal
17 valores
Percurso profissional

Outros

Categoria Profissional
Instituição de acolhimento
Empregador
2018/01/01 - Atual Senior Neurophysiology Assistant Centro Hospitalar Universitário do Porto EPE, Portugal
2017 - Atual Director of the Department of Neurophysiology Centro Hospitalar Universitário do Porto EPE, Portugal
2015 - Atual Director of the Familial Amyloidosis National Reference Centre Centro Hospitalar Universitário do Porto EPE, Portugal
1997/01/01 - Atual Director of the Familial Amyloid Polyneuropathy Clinical Unit Centro Hospitalar Universitário do Porto EPE, Portugal
1991/01/01 - Atual Coordinator of the Neuromuscular Disorders Outpatient Clinic Centro Hospitalar Universitário do Porto EPE, Portugal
2018 - 2020 Docência de ciclo de estudos especiais Centro Hospitalar Universitário do Porto EPE, Portugal
1997 - 2018 Graduate Neurophysiology Assistant Centro Hospitalar Universitário do Porto EPE, Portugal
1994/01/01 - 1997/01/01 Neurophysiology Assistant Centro Hospitalar Universitário do Porto EPE, Portugal
1987/01/01 - 1997/01/01 Regular Assistant at the Familial Amyloidosis Outpatient Clinic Centro Hospitalar Universitário do Porto EPE, Portugal
Projetos

Projeto

Designação Financiadores
2016 - Atual Natural history of transthyretin-mediated Familial Amyloidotic Polyneuropathy (TTR-FAP) and the impact of disease modifying treatments
2016/002
Investigador responsável
Centro Hospitalar Universitário do Porto EPE, Portugal
Em curso
2008 - Atual Transthyretin-Associated Amyloidoses Outcomes Survey (THAOS): A Global, Multi-Center, Longitudinal, Observational Survey of Patients with Documented Transthyretin (TTR) Mutations or Wild-Type TTR Amyloidosis
THAOS
Investigador responsável
Em curso
2006 - Atual Probing the Biochemical Mechanisms of Amyloid Disease
5 R01 DK0463365-16
Investigador
Em curso
2018/07/01 - 2021/10/31 Caracterização do citoesqueleto de actina como um novo alvo terapêutico na Polineuropatia Amiloidótica Familiar.
PTDC/MED-NEU/28336/2017
Instituto de Biologia Molecular e Celular, Portugal

Instituto Nacional de Engenharia Biomédica, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2010/04/01 - 2014/01/31 LIMP-2: da genética clínica à genómica funcional
PTDC/SAU-GMG/105344/2008
Instituto de Biologia Molecular e Celular, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2010/05/01 - 2013/10/31 Variabilidade fenotípica e genes modificadores na Polineuropatia Amiloidótica Familiar PAF ATTRV30M
PTDC/SAU-GMG/100240/2008
Instituto de Biologia Molecular e Celular, Portugal

Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal

Centro Hospitalar Universitário do Porto EPE, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2008 - 2009 Cross-Sectional Study of the Correlation between Disease Stage and Clinical Outcomes as Measured by the NIS-LL and Norfolk QOL-DN in Patients with Transthyretin-Associated Amyloidosis with Polyneuropathy (ATTR-PN)
NIS-LL QOL-DN
Investigador responsável
Concluído

Outro

Designação Financiadores
2020 - Atual ION-682884-CS3: A Phase 3 Global, Open-Label, Randomized Study to Evaluate the Efficacy and Safety of ION-682884 in Patients with Hereditary Transthyretin-Mediated Amyloid Polyneuropathy
ION-682884-CS3
Investigador responsável
Em curso
2020 - Atual HELIOS-B: A Phase 3, Randomized, Doubleblind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vutrisiran in Patients with Transthyretin Amyloidosis with Cardiomyopathy (ATTR Amyloidosis with Cardiomyopathy)
HELIOS-B
Investigador responsável
Em curso
2020 - Atual HELIOS-B: A Phase 3, Randomized, Doubleblind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Vutrisiran in Patients with Transthyretin Amyloidosis with Cardiomyopathy (ATTR Amyloidosis with Cardiomyopathy)
HELIOS-B
National Coordinator of the clinical trial
Em curso
2019 - Atual HELIOS-A: A Phase 3 Global, Randomized, Open-label Study to Evaluate the Efficacy and Safety of ALN-TTRSC02 in Patients with Hereditary Transthyretin Amyloidosis (hATTR Amyloidosis)
ALN-TTRSC02
Investigador responsável
Em curso
2019 - Atual HELIOS-A: A Phase 3 Global, Randomized, Open-label Study to Evaluate the Efficacy and Safety of ALN-TTRSC02 in Patients with Hereditary Transthyretin Amyloidosis (hATTR Amyloidosis)
ALN-TTRSC02
National Coordinator of the clinical trial
Em curso
2017 - Atual ALN-TTR02-006: A multicenter, open-label, extension study to evaluate the long-term safety and efficacy of Patisiran in patients with familial amyloidotic polyneuropathy who have completed a prior clinical study with Patisiran
ALN-TTR02-006
Investigador responsável
Em curso
2017 - Atual ALN-TTR02-006: A multicenter, open-label, extension study to evaluate the long-term safety and efficacy of Patisiran in patients with familial amyloidotic polyneuropathy who have completed a prior clinical study with Patisiran
ALN-TTR02-006
National Coordinator of the clinical trial
Em curso
2019 - 2021 ALN-TTR02-008: An Open-label Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of Patisiran-LNP in Patients with Hereditary Transthyretin-mediated Amyloidosis (hATTR Amyloidosis) with Disease Progression Post-Orthotopic Liver Transplant
ALN-TTR02-008
Investigador responsável
Em curso
2019 - 2021 ALN-TTR02-008: An Open-label Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of Patisiran-LNP in Patients with Hereditary Transthyretin-mediated Amyloidosis (hATTR Amyloidosis) with Disease Progression Post-Orthotopic Liver Transplant
ALN-TTR02-008
National Coordinator of the clinical trial
Concluído
2018 - 2020 PRX004-101: A Phase 1, Open-label, Dose Escalation Study of Intravenous PRX004 in Subjects with Amyloid Transthyretin (ATTR) Amyloidosis
PRX004-101
Investigador
Concluído
2015 - 2020 ISIS 420915-CS3: An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients with Familial Amyloid Polyneuropathy (FAP)
ISIS 420915-CS3
Investigador responsável
Concluído
2015 - 2020 ISIS 420915-CS3: An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of ISIS 420915 in Patients with Familial Amyloid Polyneuropathy (FAP)
ISIS 420915-CS3
National Coordinator of the clinical trial
Concluído
2017 - 2019 Open-label extension of ISIS 420915-CS2: A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ISI 420915 in Patients with Familial Amyloid Polyneuropathy
OL ISIS 420915-CS2
Investigador responsável
Concluído
2017 - 2019 Open-label extension of ISIS 420915-CS2: A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ISI 420915 in Patients with Familial Amyloid Polyneuropathy
OL ISIS 420915-CS2
National Coordinator of the clinical trial
Concluído
2015 - 2017 ALN-TTRSC-005: An Open-label Study to Evaluate the Efficacy and Safety of Revusiran in Patients with Transthyretin-mediated Familial Amyloidotic Polyneuropathy with Disease Progression Post Orthotopic Liver Transplant
ALN-TTRSC-005
Investigador responsável
Concluído
2015 - 2017 ALN-TTRSC-005: An Open-label Study to Evaluate the Efficacy and Safety of Revusiran in Patients with Transthyretin-mediated Familial Amyloidotic Polyneuropathy with Disease Progression Post Orthotopic Liver Transplant
ALN-TTRSC-005
National Coordinator of the clinical trial
Concluído
2014 - 2017 ALN-TTR02-004 APOLLO: A Phase 3 Multicenter, Multinational, Randomized, Doubleblind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Patisiran (ALN-TTR02) in Transthyretin (TTR)-Mediated
APOLLO
Investigador responsável
Concluído
2014 - 2017 ALN-TTR02-004 APOLLO: A Phase 3 Multicenter, Multinational, Randomized, Doubleblind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Patisiran (ALN-TTR02) in Transthyretin (TTR)-Mediated
APOLLO
National coordinator of the clinical trial
Concluído
2013 - 2017 ISIS 420915-CS2: A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ISI 420915 in Patients with Familial Amyloid Polyneuropathy
ISIS 420915-CS2
Investigador responsável
Concluído
2013 - 2017 ISIS 420915-CS2: A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ISI 420915 in Patients with Familial Amyloid Polyneuropathy
ISIS 420915-CS2
National Coordinator of the clinical trial
Concluído
2014 - 2016 ALN-TTR02-003: A Phase 2, Multicenter, Open-Label, Extension Study to Evaluate the Long-Term Safety, Clinical Activity, and Pharmacokinetics of ALN-TTR02 in Patients with Familial Amyloidotic Polyneuropathy Who Have Previously Received ALN-TTR02
ALN-TTR02-003
Investigador responsável
Concluído
2014 - 2016 ALN-TTR02-003: A Phase 2, Multicenter, Open-Label, Extension Study to Evaluate the Long-Term Safety, Clinical Activity, and Pharmacokinetics of ALN-TTR02 in Patients with Familial Amyloidotic Polyneuropathy Who Have Previously Received ALN-TTR02
ALN-TTR02-003
National Coordinator of the clinical trial
Concluído
2012 - 2014 A Phase 2, Open-Label, Multi-Dose, Dose Escalation Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intravenous Infusions of ALN-TTR02 in Patients with TTR Amyloidosis
ALN-TTR02
Investigador responsável
Concluído
2012 - 2014 A Phase 2, Open-Label, Multi-Dose, Dose Escalation Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intravenous Infusions of ALN-TTR02 in Patients with TTR Amyloidosis
ALN-TTR02
National coordinator of the clinical trial
Concluído
2009 - 2013 Open-Label Safety and Efficacy Evaluation of Fx-1006A in Patients with Transthyretin Amyloidosis
Fx-1006A ext2
Investigador responsável
Concluído
2009 - 2013 Open-Label Safety and Efficacy Evaluation of Fx-1006A in Patients with Transthyretin Amyloidosis
Fx-1006A ext2
National Coordinator of the clinical trial
Concluído
2010 - 2012 A Phase 1, Randomized, Single-Blind, Placebo-Controlled, Dose Escalation Trial to Evaluate the Safety and Tolerability of a Single Dose of Intravenous ALN-TTR01 in Patients with TTR Amyloidosis
ALN-TTR01
Investigador responsável
Concluído
2008 - 2010 An Open-Label Extension of Study Fx-005 Evaluating Long-Term Safety and Clinical Outcomes of Fx-1006A in patients with Transthyretin Amyloid Polyneuropathy
Fx-005
Investigador responsável
Concluído
2008 - 2010 An Open-Label Extension of Study Fx-005 Evaluating Long-Term Safety and Clinical Outcomes of Fx-1006A in patients with Transthyretin Amyloid Polyneuropathy
Fx-
National Coordinator of the clinical trial
Concluído
2007 - 2009 Safety and efficacy of orally administered Fx-1006A in patients with Familial Amyloid Polyneuropathy (FAP): a phase II/III, randomized, double blind placebo controlled study
Fx-1006A
Investigador responsável
Concluído
2007 - 2009 Safety and efficacy of orally administered Fx-1006A in patients with Familial Amyloid Polyneuropathy (FAP): a phase II/III, randomized, double blind placebo controlled study
Fx-1006A
National Coordinator of the clinical trial
Concluído
Produções

Publicações

Artigo em revista
  1. Sousa, Luísa; Coelho, Teresa; Taipa, Ricardo. "CNS Involvement in Hereditary Transthyretin Amyloidosis". Neurology 97 24 (2021): 1111-1119. http://dx.doi.org/10.1212/wnl.0000000000012965.
    10.1212/wnl.0000000000012965
  2. Damy, Thibaud; Conceição, Isabel; García-Pavía, Pablo; Gillmore, Julian; Jandhyala, Ravi; Sabbat, Jan; Wixner, Jonas; Coelho, Teresa. "A simple core dataset and disease severity score for hereditary transthyretin (ATTRv) amyloidosis". Amyloid 28 3 (2021): 189-198. http://dx.doi.org/10.1080/13506129.2021.1931099.
    10.1080/13506129.2021.1931099
  3. Videira, Gonçalo; Pereira, Diogo; Mota Dória, Hugo; Sousa, Ana Paula; Coelho, Teresa; Martins da Silva, Ana. "Myelopathy in hereditary ATTR Val30Met amyloidosis patients". Amyloid 28 4 (2021): 271-272. http://dx.doi.org/10.1080/13506129.2021.1927696.
    10.1080/13506129.2021.1927696
  4. Brannagan, Thomas H.; Auer-Grumbach, Michaela; Berk, John L.; Briani, Chiara; Bril, Vera; Coelho, Teresa; Damy, Thibaud; et al. "ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable". Orphanet Journal of Rare Diseases 16 1 (2021): http://dx.doi.org/10.1186/s13023-021-01834-0.
    10.1186/s13023-021-01834-0
  5. Coelho, Teresa; Ando, Yukio; Benson, Merrill D.; Berk, John L.; Waddington-Cruz, Márcia; Dyck, Peter J.; Gillmore, Julian D.; et al. "Design and Rationale of the Global Phase 3 NEURO-TTRansform Study of Antisense Oligonucleotide AKCEA-TTR-LRx (ION-682884-CS3) in Hereditary Transthyretin-Mediated Amyloid Polyneuropathy". Neurology and Therapy 10 1 (2021): 375-389. http://dx.doi.org/10.1007/s40120-021-00235-6.
    10.1007/s40120-021-00235-6
  6. Jiang, Xin; Labaudinière, Richard; Buxbaum, Joel N.; Monteiro, Cecília; Novais, Marta; Coelho, Teresa; Kelly, Jeffery W.. "A circulating, disease-specific, mechanism-linked biomarker for ATTR polyneuropathy diagnosis and response to therapy prediction". Proceedings of the National Academy of Sciences 118 9 (2021): http://dx.doi.org/10.1073/pnas.2016072118.
    10.1073/pnas.2016072118
  7. Alves-Ferreira, Miguel; Azevedo, Ana; Coelho, Teresa; Santos, Diana; Sequeiros, Jorge; Alonso, Isabel; Sousa, Alda; Lemos, Carolina. "Beyond Val30Met transthyretin (TTR): variants associated with age-at-onset in hereditary ATTRv amyloidosis". Amyloid 28 2 (2021): 100-106. http://dx.doi.org/10.1080/13506129.2020.1857236.
    10.1080/13506129.2020.1857236
  8. Adams, David; Polydefkis, Michael; González-Duarte, Alejandra; Wixner, Jonas; Kristen, Arnt V; Schmidt, Hartmut H; Berk, John L; et al. "Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study". The Lancet Neurology 20 1 (2021): 49-59. http://dx.doi.org/10.1016/s1474-4422(20)30368-9.
    10.1016/s1474-4422(20)30368-9
  9. Vilas-Boas, Maria Do Carmo; Rocha, Ana Patricia; Cardoso, Marcio Neves; Fernandes, Jose Maria; Coelho, Teresa; Cunha, Joao Paulo Silva. "Supporting the Assessment of Hereditary Transthyretin Amyloidosis Patients Based On 3-D Gait Analysis and Machine Learning". IEEE Transactions on Neural Systems and Rehabilitation Engineering 29 (2021): 1350-1362. http://dx.doi.org/10.1109/tnsre.2021.3096433.
    10.1109/tnsre.2021.3096433
  10. Dohrn, Maike F.; Ihne, Sandra; Hegenbart, Ute; Medina, Jessica; Züchner, Stephan L.; Coelho, Teresa; Hahn, Katrin. "Targeting transthyretin - Mechanism-based treatment approaches and future perspectives in hereditary amyloidosis". Journal of Neurochemistry 156 6 (2020): 802-818. http://dx.doi.org/10.1111/jnc.15233.
    10.1111/jnc.15233
  11. Liz, Marcia Almeida; Coelho, Teresa; Bellotti, Vittorio; Fernandez-Arias, Maria Isabel; Mallaina, Pablo; Obici, Laura. "A Narrative Review of the Role of Transthyretin in Health and Disease". Neurology and Therapy 9 2 (2020): 395-402. http://dx.doi.org/10.1007/s40120-020-00217-0.
    10.1007/s40120-020-00217-0
  12. Gertz, Morie; Adams, David; Ando, Yukio; Beirão, João Melo; Bokhari, Sabahat; Coelho, Teresa; Comenzo, Raymond L.; et al. "Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner". BMC Family Practice 21 1 (2020): http://dx.doi.org/10.1186/s12875-020-01252-4.
    10.1186/s12875-020-01252-4
  13. Oliveira J, Parente Freixo J, Santos M, ; Coelho, Teresa. "LAMA2 Muscular Dystrophy". In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews - Initial Posting: June 7, 2012; Last Update: September 17, 2020. (2020):
  14. Polydefkis, Michael; Gonzales-Duarte, Alejandra; Coelho, Teresa; Jonas, Wixner; Adams, David; Dinh, Quinn. "Tolérance et efficacité à long terme du Patiseran dans l'amylose héréditaire à transthyrétine". Revue Neurologique 176 (2020): S25. http://dx.doi.org/10.1016/j.neurol.2020.01.108.
    10.1016/j.neurol.2020.01.108
  15. Dyck, P. James B.; Coelho, Teresa; Waddington Cruz, Marcia; Brannagan, Thomas H.; Khella, Sami; Karam, Chafic; Berk, John L.; et al. "Neuropathy symptom and change: Inotersen treatment of hereditary transthyretin amyloidosis". Muscle & Nerve 62 4 (2020): 509-515. http://dx.doi.org/10.1002/mus.27023.
    10.1002/mus.27023
  16. Coelho, Teresa; Adams, David; Conceição, Isabel; Waddington-Cruz, Márcia; Schmidt, Hartmut H.; Buades, Juan; Campistol, Josep; et al. "A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosis". Orphanet Journal of Rare Diseases 15 1 (2020): http://dx.doi.org/10.1186/s13023-020-01399-4.
    10.1186/s13023-020-01399-4
  17. Brannagan, Thomas H.; Wang, Annabel K.; Coelho, Teresa; Waddington Cruz, Marcia; Polydefkis, Michael J.; Dyck, Peter J.; Plante-Bordeneuve, Violaine; et al. "Early Data on Long-Term Efficacy and Safety of Inotersen in Patients With Hereditary Transthyretin Amyloidosis: A 2-Year Update From the Open-Label Extension of the NEURO-TTR Trial". European Journal of Neurology (2020): http://dx.doi.org/10.1111/ene.14285.
    10.1111/ene.14285
  18. Inês, Mónica; Coelho, Teresa; Conceição, Isabel; Ferreira, Lara; de Carvalho, Mamede; Costa, João. "Health-related quality of life in hereditary transthyretin amyloidosis polyneuropathy: a prospective, observational study". Orphanet Journal of Rare Diseases 15 1 (2020): http://dx.doi.org/10.1186/s13023-020-1340-x.
    10.1186/s13023-020-1340-x
  19. Obici, Laura; Berk, John L.; González-Duarte, Alejandra; Coelho, Teresa; Gillmore, Julian; Schmidt, Hartmut H.-J.; Schilling, Matthias; et al. "Quality of life outcomes in APOLLO, the phase 3 trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosis". Amyloid (2020): 1-10. http://dx.doi.org/10.1080/13506129.2020.1730790.
    10.1080/13506129.2020.1730790
  20. Merlini, Giampaolo; Coelho, Teresa; Waddington Cruz, Márcia; Li, Huihua; Stewart, Michelle; Ebede, Ben. "Evaluation of Mortality During Long-Term Treatment with Tafamidis for Transthyretin Amyloidosis with Polyneuropathy: Clinical Trial Results up to 8.5 Years". Neurology and Therapy 9 1 (2020): 105-115. http://dx.doi.org/10.1007/s40120-020-00180-w.
    10.1007/s40120-020-00180-w
  21. González-Duarte, Alejandra; Berk, John L.; Quan, Dianna; Mauermann, Michelle L.; Schmidt, Hartmut H.; Polydefkis, Michael; Waddington-Cruz, Márcia; et al. "Correction to: Analysis of autonomic outcomes in APOLLO, a phase III trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosis". Journal of Neurology 267 3 (2020): 713-714. http://dx.doi.org/10.1007/s00415-020-09715-5.
    10.1007/s00415-020-09715-5
  22. Adams, David; Ando, Yukio; Beirão, João Melo; Coelho, Teresa; Gertz, Morie A.; Gillmore, Julian D.; Hawkins, Philip N.; et al. "Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy". Journal of Neurology 268 6 (2020): 2109-2122. http://dx.doi.org/10.1007/s00415-019-09688-0.
    10.1007/s00415-019-09688-0
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  87. Coelho, Teresa; Maia, Luis F.; da Silva, Ana Martins; Cruz, Márcia W.; Planté-Bordeneuve, Violaine; Suhr, Ole B.; Conceiçao, Isabel; et al. "Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy". Journal of Neurology 260 11 (2013): 2802-2814. http://dx.doi.org/10.1007/s00415-013-7051-7.
    10.1007/s00415-013-7051-7
  88. Planté-Bordeneuve, V.; Hachulla, E.; Vuillemet, F.; Coelho, Teresa; Rapezzi, C.; Suhr, O.; Karayal, O.. "L’observatoire international pour l’amylose à transthyrétine (TTR) THAOS : une nouvelle fenêtre sur la maladie et ses traitements". Revue Neurologique 169 (2013): A51. http://dx.doi.org/10.1016/j.neurol.2013.01.114.
    10.1016/j.neurol.2013.01.114
  89. Ando, Yukio; Coelho, Teresa; Berk, John L; Cruz, Márcia Waddington; Ericzon, Bo-Göran; Ikeda, Shu-ichi; Lewis, W David; et al. "Guideline of transthyretin-related hereditary amyloidosis for clinicians". Orphanet Journal of Rare Diseases 8 1 (2013): 31. http://dx.doi.org/10.1186/1750-1172-8-31.
    10.1186/1750-1172-8-31
  90. Coelho, Teresa; Maurer, Mathew S.; Suhr, Ole B.. "THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis". Current Medical Research and Opinion 29 1 (2012): 63-76. http://dx.doi.org/10.1185/03007995.2012.754348.
    10.1185/03007995.2012.754348
  91. Planté-Bordeneuve, Violaine; Suhr, Ole B.; Maurer, Mathew S.; White, Barbara; Grogan, Donna R.; Coelho, Teresa. "The Transthyretin Amyloidosis Outcomes Survey (THAOS) registry: design and methodology". Current Medical Research and Opinion 29 1 (2012): 77-84. http://dx.doi.org/10.1185/03007995.2012.754349.
    10.1185/03007995.2012.754349
  92. Coelho, T.; Maia, L. F.; Martins da Silva, A.; Waddington Cruz, M.; Plante-Bordeneuve, V.; Lozeron, P.; Suhr, O. B.; et al. "Tafamidis for transthyretin familial amyloid polyneuropathy: A randomized, controlled trial". Neurology 79 8 (2012): 785-792. http://dx.doi.org/10.1212/wnl.0b013e3182661eb1.
    10.1212/wnl.0b013e3182661eb1
  93. Coelho, Teresa. "Female Sexual and Pelvic Floor Muscles Dysfunctions in Familial Amyloidotic Polyneuropathy (FAP-Portuguese Type)". Arch Esp Urol. 2012 May;65(4):476-88. 65 4 (2012): 476-488.
    Publicado
  94. Azevedo, Elsa; Castro, Pedro; Santos, Rosa; Freitas, João; Coelho, Teresa; Rosengarten, Bernhard; Panerai, Ronney. "Autonomic dysfunction affects cerebral neurovascular coupling". Clinical Autonomic Research 21 6 (2011): 395-403. http://dx.doi.org/10.1007/s10286-011-0129-3.
    10.1007/s10286-011-0129-3
  95. Santos, Rosário; Oliveira, Jorge; Vieira, Emília; Coelho, Teresa; Carneiro, António Leite; Evangelista, Teresinha; Dias, Cristina; et al. "Private dysferlin exon skipping mutation (c.5492G>A) with a founder effect reveals further alternative splicing involving exons 49–51". Journal of Human Genetics 55 8 (2010): 546-549. http://dx.doi.org/10.1038/jhg.2010.60.
    10.1038/jhg.2010.60
  96. Do Amaral, Barbas; Coelho, T.; Sousa, A.; Guimarães, A.. "Usefulness of labial salivary gland biopsy in familial amyloid polyneuropathy Portuguese type". Amyloid 16 4 (2009): 232-238. http://dx.doi.org/10.3109/13506120903421850.
    10.3109/13506120903421850
  97. Oliveira, J; Santos, R; Soares-Silva, I; Jorge, P; Vieira, E; Oliveira, ME; Moreira, A; et al. "LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients". Clinical Genetics 74 6 (2008): 502-512. http://dx.doi.org/10.1111/j.1399-0004.2008.01068.x.
    10.1111/j.1399-0004.2008.01068.x
  98. Munar-Qués, Miguel; Masjuan, Jaime; Coelho, Teresa; Moreira, Paul; Viader-Farré, Carlos; Saraiva, María J. M.. "Familial amyloid polyneuropathy associated with TTRSer50Arg mutation in two Iberian families presenting a novel single base change in the mutant gene". Amyloid 14 2 (2007): 147-152. http://dx.doi.org/10.1080/13506120701259580.
    10.1080/13506120701259580
  99. Maria isabela Sá; sofia cabral; P Dias Costa; Coelho, Teresa; Mário Freitas; Severo Torres; J Lopes Gomes. "Cardiac involvement in type 1 myotonic dystrophy". Rev Port Cardiol 9 26 (2007): 829-840.
    Publicado
  100. Martins, L.; Pedroso, S.; Henriques, A.C.; Dias, L.; Sarmento, A.M.; Seca, R.; Oliveira, F.; et al. "Simultaneous Pancreas-Kidney Transplantation: Five-Year Results From a Single Center". Transplantation Proceedings 38 6 (2006): 1929-1932. http://dx.doi.org/10.1016/j.transproceed.2006.06.089.
    10.1016/j.transproceed.2006.06.089
  101. Soares, Miguel L.; Coelho, Teresa; Sousa, Alda; Batalov, Serge; Conceição, Isabel; Sales-Luís, Maria L.; Ritchie, Marylyn D.; et al. "Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease". Human Molecular Genetics 14 4 (2005): 543-553. http://dx.doi.org/10.1093/hmg/ddi051.
    10.1093/hmg/ddi051
  102. Martins Da Silva, A.; Rocha, N.; Pinto, M.; Alves, V.; Farinha, F.; Correia, A.P.; Coelho, T.; Magalhães, M.. "Tremor as the first neurological manifestation of Sneddon's syndrome". Movement Disorders 20 2 (2004): 248-251. http://dx.doi.org/10.1002/mds.20270.
    10.1002/mds.20270
  103. Soares, Miguel Luz; Coelho, Teresa; Sousa, Alda; Holmgren, Gösta; Saraiva, Maria João; Kastner, Daniel L; Buxbaum, Joel N. "Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype–phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden". European Journal of Human Genetics 12 3 (2003): 225-237. http://dx.doi.org/10.1038/sj.ejhg.5201095.
    10.1038/sj.ejhg.5201095
  104. Martins, L; Henriques, A; Dias, L; Ventura, A; Seca, R; Almeida, R; Dores, J; et al. "Combined pancreas-kidney transplantation". Transplantation Proceedings 35 3 (2003): 1107-1108. http://dx.doi.org/10.1016/s0041-1345(03)00327-0.
    10.1016/s0041-1345(03)00327-0
  105. Paula Mendes; Isabel Meneses; Luís Monteiro; Coelho, Teresa; Cristiana Vasconcelos; Manuela Lemos; Rita Ferreira; Maria Clara Sá Miranda. "Evolução fenotípica na adrenoleucodistrofia [Phenotypic evolution in adrenoleukodystrophy]". Acta Med Port. 16 4 (2003): 285-288.
    Publicado
  106. Guimarães, Carla P.; Lemos, Manuela; Menezes, Isabel; Coelho, Teresa; Sá-Miranda, Clara; Azevedo, Jorge E.. "Characterisation of two mutations in the ABCD1 gene leading to low levels of normal ALDP". Human Genetics 109 6 (2001): 616-622. http://dx.doi.org/10.1007/s00439-001-0632-z.
    10.1007/s00439-001-0632-z
  107. Paula Mendes; Isabel Meneses; Coelho, Teresa; Manuela Lemos; Rita Ferreira. "Adrenoleucodistrofia: incidência e frequência relativa dos seus fenótipos. Experiência do Serviço de Endocrinologia do HGSA (1987 a 1999).". Arquivos de Medicina 15 (2001): 114-117.
    Publicado
  108. Coelho, T (C71E-3343-F445); Munar-Qués M, Pedrosa JL, Coelho T, Gusmão L, Seruca R, Amorim A, Sequeiros J.. "Two Pairs of Proven Monozygotic Twins Discordant for Familial Amyloid Neuropathy (FAP) TTR Met 30". Journal of Medical Genetics 36 8 (1999): 629-632.
    Publicado
  109. Soares, Miguel; Buxbaum, Joel; Sirugo, Giorgio; Coelho, Teresa; Sousa, Alda; Kastner, Daniel; João Saraiva, Maria. "Genetic anticipation in Portuguese kindreds with familial amyloidotic polyneuropathy is unlikely to be caused by triplet repeat expansions". Human Genetics 104 6 (1999): 480-485. http://dx.doi.org/10.1007/s004390050991.
    10.1007/s004390050991
  110. Coelho, Teresa; Munar-Qués, Miguel; Pedrosa, JL; Gusmão, L; Seruca, R; Amorim, A; Sequeiros, J.. "Two pairs of proven monozygotic twins discordant for familial amyloid neuropathy (FAP) TTR Met 30". 36 8 (1999): 629-632.
    Publicado
  111. Beirao, I.; Lobato, L.; Guimaraes, S.; Cardoso, P.; Costa, P.; Coelho, T.; Rocha, G.. "Early destructive spondyloarthropathy from combined  2-microglobulin and transthyretin Met30 amyloidosis in a dialysed patient". Nephrology Dialysis Transplantation 13 12 (1998): 3223-3225. http://dx.doi.org/10.1093/ndt/13.12.3223.
    10.1093/ndt/13.12.3223
  112. Vilarinho, Laura; Santorelli, Filippo M.; Cardoso, Maria Luís; Coelho, Teresa; Guimarães, António; Coutinho, Paula. "Mitochondrial DNA Analysis in Ocular Myopathy". European Neurology 39 3 (1998): 148-153. http://dx.doi.org/10.1159/000007925.
    10.1159/000007925
  113. Vilarinho, L.; Maia, C.; Coelho, T.; Coutinho, P.; Santorelli, F. M.. "Heterogeneous presentation in Leigh syndrome". Journal of Inherited Metabolic Disease 20 5 (1997): 704-705. http://dx.doi.org/10.1023/a:1005330611147.
    10.1023/a:1005330611147
  114. Vilarinho, L; Maia, C; Coelho, Teresa; Coutinho, P; Santorelli, FM. "Estudo das citopatias mitocondriais. Parte I.". Arquivos de Medicina, 1997, 11:75-81. 11 (1997): 75-81.
    Publicado
  115. Vilarinho, L; Cardoso, ML; Coelho, Teresa; Matos, I; Coutinho, P; Guimarães, A. "Estudo das citopatias mitocondriais. Parte II. Revisão de 30 Doentes". Arquivos de Medicina 11 (1997): 160-166.
    Publicado
  116. Coelho, Teresa. "Familial Amyloid Polyneuropathy: New Developments in Genetics and Treatment". Curr Opin Neurol 9 5 (1996): 355-359.
    Publicado
  117. Sousa, Alda; Coelho, Teresa; Barros, José; Sequeiros, Jorge. "Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type I in Póvoa do Varzim and Vila do Conde (north of Portugal)". American Journal of Medical Genetics 60 6 (1995): 512-521. http://dx.doi.org/10.1002/ajmg.1320600606.
    10.1002/ajmg.1320600606
  118. Sampaio, C; Coelho, Teresa; Castro-Caldas, A; Bastos-Lima, A; Levy, A. "The response of "de novo" Parkinson's disease patients to bromocriptine in a "low and slow" regimen is predictive for prognosis". J Neural Transm 45 (1995): 197-202.
    Publicado
  119. Monteiro, L; Silveira, A; Sampaio-Silva, ML; Correia, JM; Costa, AM; Carvalho, MT; Coelho, JM; Coelho, Teresa. "Teníase/cisticercose por Taenia solium: estudo epidemiológico piloto numa aldeia do Norte de Portugal". Revista Portuguesa de Doenças Infecciosas 18 (1995): 182-188.
    Publicado
  120. Coelho, T; Sousa, A; Lourenco, E; Ramalheira, J. "A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected.". Journal of Medical Genetics 31 4 (1994): 293-299. http://dx.doi.org/10.1136/jmg.31.4.293.
    10.1136/jmg.31.4.293
  121. Alves, I L; Divino, C M; Schussler, G C; Altland, K; Almeida, M R; Palha, J A; Coelho, T; Costa, P P; Saraiva, M J. "Thyroxine binding in a TTR Met 119 kindred.". The Journal of Clinical Endocrinology & Metabolism 77 2 (1993): 484-488. http://dx.doi.org/10.1210/jcem.77.2.8102146.
    10.1210/jcem.77.2.8102146
  122. Monteiro, L; Coelho, Teresa; Stocker, A. "Neurocysticercosis--a review of 231 cases". Infection 20 (1992): 61-65.
    Publicado
  123. Almeida-Pinto, J; Veiga-Pires, JA; Stocker, A; Coelho, Teresa; Monteiro, L. "Cysticercosis of the brain. The value of computed tomography". Acta Radiol 29 (1988): 625-628.
    Publicado
  124. Monteiro, L; Coelho, Teresa; Stocker, A. "[Neurocysticercosis, a frequent parasitic disease in Portugal. 138 cases diagnosed by brain scanning]". Presse Med 16 (1987): 964-964.
    Publicado
  125. Lima, AB; Fontes, AC; Guimarães, A; Justiça, B; Reis, F; Leal, I; Rocha-Melo, J; Campos, M; Coelho, Teresa. "Infecção fúngica do Sistema Nervoso Central – a Propósito de um Caso de Aplasia Medular". Médico 116 (1987): 46-54.
    Publicado
Capítulo de livro
  1. Coelho, Teresa. "A Experiência do Aconselhamento Genético na Polineuropatia Amiloidótica Familiar". In O Teste Preditivo na Doença De Machado-Joseph, editado por Sequeiros, Jorge, 71-77. Instituto de Biologia Molecular e Celular, 1996.
    Publicado
  2. Sousa, A.; Coelho, T.; Sequeiros, J.. "Parental Transmission and Age-of-Onset in Familial Amyloidotic Polineuropathy (Portuguese Type)". In Amyloid and Amyloidosis 1990, 691-693. Springer Netherlands, 1991.
    10.1007/978-94-011-3284-8_170
  3. Sequeiros, J.; Sousa, A.; Coelho, T.. "Sex Differences and Age-Dependent Penetrance in FAP-Type I". In Amyloid and Amyloidosis 1990, 687-690. Springer Netherlands, 1991.
    10.1007/978-94-011-3284-8_169
  4. Sousa, A.; Coelho, T.; Lobato, L.; Sequeiros, J.. "Anticipation of Age-of-Onset in Familial Amyloidotic Polineuropathy (Portuguese Type)". In Amyloid and Amyloidosis 1990, 694-697. Springer Netherlands, 1991.
    10.1007/978-94-011-3284-8_171
  5. Carvalho, M.; Freitas, J.; Puig, J.; Coelho, Teresa; Fernandes, P.; Costa, O.; de Freitas, Falcão; Coelho, T.. "Spectral Analysis of R-R Variability in Familial Amyloidotic Polyneuropaty, Andrade Type". In Amyloid and Amyloidosis 1990, editado por Natvig J.B. et al., 839-842. Springer Netherlands, 1991.
    Publicado • 10.1007/978-94-011-3284-8_206
  6. Coelho, Teresa; Morgado, R; Coutinho, P. "Statistical Analysis of Factors which May Influence the Duration of FAP -1". In Familial Amyloidotic Polyneuropathy and other TTR Related Disorders, editado por Costa, PP; Freitas AF; Saraiva, MJ, 351-355. Arquivos de Medicina, 1990.
    Publicado
  7. Amorim, P; Araujo, I; Coelho, Teresa; Freitas, AF; Araujo, S. "Cardiovascular Disorders in FAP Patients Under General Anaesthesia for Surgical Procedures". In Familial Amyloidotic Polyneuropathy and other TTR Related Disorders, editado por Costa, PP; Freitas, AF; Saraiva, MJ, 305-310. Arquivos de Medicina, 1990.
    Publicado
Poster em conferência
  1. Souto Silva, Renata; Oliveira, Vanessa; Sousa, Ana Paula; Cardoso, Márcio; Garrido, Cristina; Coelho, Teresa; Santos, Manuela. "Atrofia Muscular Espinhal Tipos 1 a 4. Caracterização dos doentes do Centro Hospitalar do Porto". Trabalho apresentado em Congresso de Neurologia 2018, 2018.
  2. Armindo Fernandes; Coelho, Teresa; Aurora Rodrigues; Helena Felgueiras; Pedro Oliveira; Antonio Guimaraes; Manuel Melo Pires; Ricardo Taipa. "Correlacoes Clinico-Patologicas nas Biopsias de Nervo Sural na Polineuropatia Amiloidotica Familiar por Transtirretina". Trabalho apresentado em Congresso de Neurologia 2018, 2018.
  3. Gonzalez Duarte, A; Coelho, Teresa; Adams, D; Yang, C; Polydefkis, M; Kristen, A; Tournev, I; et al. "Long-term use of Patisiran, an investigational RNAi therapeutic, in patients with Hereditary Transthyretin-Mediated Amyloidosis: 12 month efficacy and safety data from Global Open Label Extension (Ole) Study". Trabalho apresentado em American Association Of Neuromuscular & Electrodiagnostic Medicine Annual Meeting 2018, 2018.
  4. Quan, D; Adams, D; Gonzalez Duarte, A; Polydefkis, M; Kristen, A; Tournev, I; Schmidt, H; et al. "Evaluating the impact of Patisiran on disability using The Rasch-Built Overalldisability Scale (R-Ods) in patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis in the Apollo Study". Trabalho apresentado em American Association Of Neuromuscular & Electrodiagnostic Medicine Annual Meeting 2018, 2018.
  5. Gertz, M; Wang, A; Coelho, Teresa; Waddington Cruz, M; Polydefkis M, Dyck P, Scheinberg M, Plante Bordeneuve V, Berk J, Barroso F, Adams D, Brannagan T, Whelan C, Merlini G,; Drachman B, Bheitner S, Conceicao I, Schmidt H, Vita G, Campistol J, Gorevic P, Monia B, Hughes S, Kwoh J,; Mcevoy B, Jackermann E, Benson M. "Safety and efficacy of Inotersen in patients with Hereditary Transthyretinamyloidosis with Polyneuropathy (Neuro-Ttr)". Trabalho apresentado em American Association of Neuromuscular & Electrodiagnostic Medicine Annual Meeting 2018, 2018.
  6. Polydefkis, M; Coelho, Teresa; Waddington Cruz, M; Dyck, P; Scheinberg M, Plante Bordeneuve V, Berk J, Barroso F, Adams D, Brannagan T,; Whelan C, Merlini G, Drachman B, Heitner S, Conceicao I, Schmidt H, Vita G,; Campistol J, Gorevic P, Monia B, Hughes S, Kwoh J, Mcevoy B, Ackermann E, Gertz M, Benson M, Wang A. "Inotersen improves Modified Neuropathy Impairment Scores plus 7 Measures in patients with Hereditary Transthryetin (hATTR) Amyloidosis in The Phase 3 Study (Neuro-TTR)". Trabalho apresentado em American Association of Neuromuscular & Electrodiagnostic Medicine Annual Meeting 2018, 2018.
  7. Brannagan, T; Wang, A; Coelho, Teresa; Waddington Cruz, M; Polydefkis M, Dyck P, Scheinberg M, Plante Bordeneuve V, Berk J, Barroso F, Adams D, Whelan C, Merlini G, Drachman B,; Heitner S, Conceicao I, Schmidt H, Vita G, Campistol J, Gorevic P, Monia B, Hughes S, Kwoh J, Mcevoy B,; Ackermann E, Benson M, Gertz M. "Open Label Extension of the Phase 3 Study Neuro-TTR to assess the long-term efficacy and safety of Inotersen in patients wth Hereditary Transthyretin Amyloidosis". Trabalho apresentado em American Association of Neuromuscular & Electrodiagnostic Medicine Annual Meeting 2018, 2018.
  8. Oliveira Santos, M; Falcao de Campos, C; Garrido, C; Palavra, F; Negrao, L; Vieira, JP; Mendonca, C; Coelho, Teresa; Fineza I, Santos M, Moreno T. "Clinical and molecular features of Proximal Spinal Muscle Atrophy in Portugal: A Multicentre Retrospective Study". Trabalho apresentado em 23rd International Annual Congress Of The World Muscle Society, 2018.
  9. Taipa, R; Martins da Silva, A; Lobato, L; Vizcano, R; Alves, J; Coelho, Teresa; Melo Pires, M. "Early Central Nervous System Involvement In V30M ATTR Amyloidosis Patient". Trabalho apresentado em 19th International Congress Of Neuropathology - Japan, 2018, 2018.
  10. Grogan, M; Adams, D; Coelho, Teresa; Kristen, A; Dispenzieri, A; Solomon, S; Gollob, J; et al. "NT-ProBNP levels in patients with Hereditary Transthyretin-Mediated Amyloidosis treated in the Phase 3 Apollo Study based on diuretic use". Trabalho apresentado em 22nd Annual Scientific Meeting of the Heart Failure Society of America - Nashville, USA, 2018.
  11. Gertz, M; Wang, A; Coelho, Teresa; Waddington Cruz, M; Polydefkis M, Dyck P, Scheinberg M, Plante Bordeneuve V, Berk J, Barroso F, Brannagan T, Khella S, Conceicao I,; Gorevic P, Monia B, Benson M. "Safety and efficacy of Inotersen in patients with Hereditary Transthyretin Amyloidosis with Polyneuropathy (Neuro-TTR)". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  12. Coelho, Teresa; Suhr, O; Quan, D; Brannagan, T; Gollob J, Goyal S, Altincatal A, Agarwal S, Lin H, Adams D. "Longitudinal changes in MNIS 7 are associated with changes in ambulatory status in Hereditary Transthyretin Mediated Amyloidosis". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  13. Gonzalez Duarte, A; Adams, D; Oriordan, W; Yang, C; Yamashita, T; Kristen, A; Tournev, I; et al. "Changes in neuropathy stage in patients with Hattr Amyloidosis following treatment with Patisiran: Analysis from Apollo". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  14. Coelho, Teresa; Brannagan, T; Wang, A; Waddington Cruz M, Polydefkis, M, Dyck P, Plante Bordeneuve V, Berk J, Barroso F, Adams D, Merlini G, Conceicao, I; Monia B, Hughes S, Kwoh J, Jung S, Baker B, Ackerman E, Benson M, Gertz M. "Long-term efficacy and safety of Inotersen in patients with Hereditary Transthyretin (hATTR) Amyloidosis treated in the open label extension of the Phase 3 Study Neuro-TTR". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  15. Coelho, Teresa; Flynn A, Ebede B, Rill D, Sultan M, Li H, Huber P. "Comprehensive safety profile of Tafamidis". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  16. Dick, P; Wang, A; Coelho, Teresa; Waddington Cruz M, Polydefkis M, Gertz M, Sheinberg M, PanteBordeneuve V, Berk J, Barroso F, Brannagan T, Khella S,; Conceicao I, Gorevic P, Monia B, Benson M. "Inotersen improved Quality of Life and neuropathy measures across levels of transthyretin reduction (Neuro-TTR)". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  17. Monteiro, C; Martins da Silva, A; Rodrigues, C; Anselmo, J; Fernandes, J; Coelho, Teresa. "Development and validation of The Transthyretin Familial Amyloid Polyneuropapathy Score (TTR-FAP Score)". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  18. Sousa, A.; Valdrez, K; Anselmo, J; Cardoso, M; Coelho, Teresa. "Comparison of Sudoscan, QSART and SSR in the evaluation of sudomotor dysfunction". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  19. Polydefkis, M; Adams, D; Coelho, Teresa; Kristen A, Gonzalez Duarte A, Berk J, Quan D, Partisano A, Gollob J, Sweester M, Chen J, Suhr O. "Infusion related reactions in patients with hATTR Amyloidosis treated with Patisiran". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  20. Brannagan, T; Wang, A; Coelho, Teresa; Waddington Cruz M, Polydefkis M, Dyck M, Plante Bordeneuve V, Berk J, Barroso F, Adams D, Merlini G, Conceicao I,; Monia B, Hughes S, Kwoh J, Jung S, Baker B, Ackerman E, Benson M, Gertz M. "Indirect comparision of Patisiran and Tafamidis for treatment of Hereditary Transthyretin Mediated (hATTR) Amyloidosis with Polyneuropathy". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  21. Dyck, P; Adams, D; Coelho, Teresa; Polydefkis M, Gonzalez Duarte A, Kristen A, Berk J, Partisano A, Gollob J, Sweester M, Chen J, Suhr O. "Neuropathy progression in patients with hATTR Amyloidosis. Analysis of the Apollo placebo arm". Trabalho apresentado em 2018 Peripheral Nerve Society Annual Meeting - Baltimore, USA, 2018.
  22. Sousa, L.; Santos, E.; Martins, J.; Sousa, A.; Cardoso, M.; Silveira, F.; Naidais, G.; et al. "Congenital myasthenic syndromes in a subpopulation of the north of portugal". Trabalho apresentado em 15th International Congress on Neuromuscular Diseases, Vienna, Austria, 2018.
  23. Mauermann, M; Adams, D; Gonzalez Duarte, A; Coelho, Teresa; Yang C, Polydefkis M, Kristen A, Tournev I, Schmidt H, Berk J, Lin K, Gandhi P, Sweetser M, White M, Gollob J, Suhr O. "Impact of Patisiran on Autonomic Neuropathy in Hereditary Transthyretin Mediated Amyloidosis". Trabalho apresentado em 15th International Congress on Neuromuscular Diseases - Vienna, Austria, 2018.
  24. Coelho, Teresa; Adams, D; Gonzalez Duarte, A; Oriordan, W; Yang C, Polydefkis M, Kristen A, Tournev I, Schmidt H, Berk J, Lin K, Gandhi P, Sweetser M, Powell C, Gollob J, Suhr O. "Transthyretin reduction with Patisiran in The Apollo Phase 3 study". Trabalho apresentado em 15th International Congress on Neuromuscular Diseases - Vienna, Austria, 2018.
  25. Obici, L; Coelho, Teresa; Adams, D; Gonzalez Duarte, A; Oriordan W, Yang C, Arnt K, Tournev I, Schmidt H, Berk J, Lin K, Gandhi P, Sweetser M, Lin T, Gollob J, Suhr O. "Apollo Phase 3 Study: Impact of baseline neuropathy severity on response to Patisiran". Trabalho apresentado em 15th International Congress on Neuromuscular Diseases - Vienna, Austria, 2018.
  26. Cavaco, S; Martinsda Silva, A; Fernandes, J; Samoes, R; Alves, C; Cardoso, M; Kelly, J; Monteiro, C; Coelho, Teresa. "Age-dependent cognitive dysfunction in untreated and liver transplanted ATTR V30M patients". Trabalho apresentado em 4th Congress Of The European Academy Of Neurology - Lisboa, Portugal, 2018.
  27. Coelho, Teresa; Rapezzi, C. "Developing a framework to optimise the ongoing assessment of ATTR- Amyloidosis in patients with a cardiac phenotype". Trabalho apresentado em 4th Congress Of The European Academy Of Neurology - Lisboa, Portugal, 2018.
  28. Parman, Y; Coelho, Teresa; Conceicao, I; Galn, L; Obici, L; Rousseau, A. "Developing a framework to optimise the ongoing assessment of ATTR- Amyloidosis". Trabalho apresentado em 4th Congress Of The European Academy Of Neurology -Lisboa, Portugal, 2018.
  29. Berk, J; Coelho, Teresa; Ak, W; Waddington Cruz, M; Polydefkis,M, Dyck P, Scheinberg M, PlanteBordeneuve V, Barroso F, Adams D, Brannagan T, Whelan C,; Merlini G, Drachman B, Heitner S, Conceicao I, Schmidt H, Vita G, Campistol J,Gorevic P, Monia B, Hughes S, Kwoh J,; Jung B, Ackermann E, Gertz M, Benson M. "Inotersen improves quality of life and neuropathy in patients with Hereditary Transthyretin (hATTR) Amyloidosis with Polyneuropathy: Results of the Phase 3 Study Neuro-TTR". Trabalho apresentado em ISPOR 2018 - Boston, USA, 2018.
  30. Coelho, Teresa; Slama, M; Solomon, S; Adams, D; Damy T, Merlini G, Grogan M, Maurer M, Partisano A, Chen J, Karsten V, Vest J, Suhr O, Kristen A. "Analysis of NT-ProBNP baseline levels in Apollo as a predictor of survival in Hereditary Transthyretin-Mediated (hATTR) Amyloidosis". Trabalho apresentado em European Society Of Cardiology - Heart Failure 2018, 2018.
  31. Berk, J; Wang, A; Coelho, Teresa; Waddington Cruz M, Polydefkis M, Dyck P, Scheinberg M, PlanteBordeneuve V, Barroso F, Adams D, Brannagan T, Whelan C,; Drachman B, Heitner S, Conceicao I, Schmidt H, Vita G, Campistol J, Gamez J, Gane E, Gorevic P; Bulle Oliveira A, Monia B, Hughes S, Kwoh J, Mcevoy B, Baker B, Jackermann E, Guthrie S, Kessler A; Gertz M, Benson M, Merlini G. "Burden of Hereditary Transthyretin Amyloidosis with Polyneuropathy in patients enrolled in the Phase 3 Study Neuro-TTR". Trabalho apresentado em 70th American Academy of Neurology Annual Meeting - Los Angeles, USA, 2018.
  32. Coelho, Teresa; Brannagan, T; Wang, A; Waddington Cruz M, Polydefkis M, Dyck P, Scheinberg M, Berk J, Barroso F, Adams D, Whelan C, Merlini G,; Drachman H, Heitner S, Conceicao I, Schmidt H, Vita G, Campistol J, Gamez J, Gorevic P, Monia B, Hughes S, Kwoh J,; Mcevoy B, Baker B, Ackermann E, Benson M, Gertz M. "Open label extension of the Phase 3 Study Neuro-TTR to assess the long-termefficacy and safety of Inotersen in patients with Hereditary Transthyretin Amyloidosis". Trabalho apresentado em 70th American Academy of Neurology Annual Meeting - Los Angeles, USA, 2018.
  33. Gonzalez Duarte, A; Adams, D; Oriordan, W; Yang, C; Yamashita, T; Kristen, A; Tournev, I; et al. "Changes in neuropathy stage in patients with Hereditary Transthyretin mediated amyloidosis following treatment with Patisiran, an investigational RNAi therapeutic: An analysis from the Phase 3 Apollo Study". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  34. Berk, J; Lin, H; Agarwal, S; Merkel, M; Gollob, J; Berger, A; Shah, S; et al. "Impact of Hereditary Transthyretin-Mediated Amyloidosis on use of healthcare services. An analysis of the Apollo Study". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  35. Berk, J; Lin, H; Agarwal, S; Merkel, M; Gollob, J,; Berger, A; Shah, S; et al. "Impact of Hereditary Transthyretin-Mediated Amyloidosis on daily living and work productivity: Baseline results from Apollo". Trabalho apresentado em XVIth International Symposium on Amyloidosis I- Kumamoto, Japan, 2018.
  36. Suhr, O; Gonzalez Duarte, A; Oriordan, W; Yang, C; Yamashita, T; Kristen, A; Tournev, I; et al. "Long-term use of patisiran, an investigational RNAi therapeutic, in patients with Hereditary Transthyretin mediated Amyloidosis: Baseline demographics and preliminary data from global open label extension study". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  37. Lemos, Carolina; Coelho, Teresa. "The role of genetic factors of Alzheimer and Parkinson Disease as modulators of age at onset on Familial Amyloid Polyneuropathy". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  38. Coelho, Teresa; Adams, D; Gonzalez Duarte, A. "Patisiran, an investigational RNAi therapeutic for patients with Hereditary Transthyretin-Mediated Amyloidosis: regional and genotypic subgroup analyses from the Apollo Study". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  39. Sousa, Ana Paula; Valdrez, Kátia; Cardoso, Márcio; Anselmo, João; Freitas, Mónica; Ferreira, Hélder; Coelho, Teresa. "The diagnostic utility of neurophysiologic tests for early diagnostic of Transthyretin Familial Amyloid Polyneuropathy". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  40. Sousa, Ana Paula; Valdrez, Kátia; Alves, Cristina; Martins da Silva, Ana; Coelho, Teresa. "The diagnostic value of unspecific clinical features in the follow-up of Val30Met TTR mutation carriers". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  41. Brannagan, T; Wang, A; Coelho, Teresa; Waddington Cruz, M; Polydefkis M, Dyck P, Scheinberg M, Plante Bordeneuve V, Berk J, Barroso F, Adams D, Whelan C, Merlini G, Drachman B,; Heitner S, Conceicao I, Schmidt H, Vita G, Campistol J, Gorevic P, Monia B, Hughes S, Kwoh J, Mcevoy B,; Ackermann E, Benson M, Gertz M. "Open Label Extension of the Phase 3 Study Neuro-TTR to assess the long-term efficacy and safety of Inotersen in patients with Hereditary Transthyretin Amyloidosis (hATTR)". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  42. Damy, T; Conceicao, I; Planté-Bordeneuve, V; Mundayat, R; Schumacher, J; Coelho, Teresa. "Cardiac disorders in THAOS subjects with V30M Transthyretin Amyloidosis". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  43. Polydefkis, M; Coelho, Teresa; Waddington Cruz, M; Dyck, P; Scheinberg M, Planté-Bordeneuve V, Berk J, Barroso F, Adams D, Brannagan T, Whelan C, Merlini G, Drachman B, Heitner S,; Conceicao I, Schmidt H, Vita G, Campistol J, Gamez J, Gane E, Gorevic P, Souza Bulle Oliveira A, Monia B, Hughes S; Kwoh J, Mcevoy B, Baker B, Ackermann E, Gertz M, Benson M, Wang A. "Inotersen improves Norfolk Quality of Life-Diabetic Neuropathy Measures in patients with Hereditary Transthyretin Amyloidosis with Polyneuropathy in the Phase3 Study Neuro-TTR". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  44. Berk, J; Wang, A; Coelho, Teresa; Waddington Cruz M, Polydefkis M, Dyck P, Scheinberg M, PlanteBordeneuve V, Barroso F, Adams D, Brannagan T, Whelan C,; Drachman B, Heitner S, Conceicao I, Schmidt H, Vita G, Campistol J, Gamez J, Gane E, Gorevic P, Souza Bulle Oliveira A; Monia B, Hughes S, Kwoh J, Mcevoy B, Baker B, Jackermann E, Guthrie S, Kessler A; Gertz M, Benson M, Merlini G. "Burden of Hereditary Transthyretin Amyloidosis with Polyneuropathy in patients enrolled in the Phase 3 Study Neuro-TTR". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  45. Gertz, M; Wang, A; Coelho, Teresa; Waddington Cruz M, Polydefkis M, Dyck P, Scheinberg M, Plante Bordeneuve V, Berk J,. "Safety and efficacy of Inotersen in patients with Hereditary Transthyretin Amyloidosis with Polyneuropathy (Neuro-TTR)". Trabalho apresentado em XVIth International Symposium on Amyloidosis - Kumamoto, Japan, 2018.
  46. Oliveira, J; Cardoso, M; Taipa, R; Goncalves, A; Oliveira, M; Melo Pires, M; Santos, M.; Coelho, Teresa; Santos, R.. "The expanding phenotype of LAMA2-Related muscular dystrophies. Four additional cases diagnosed during adulthood". Trabalho apresentado em 21st International Congress Of The World Muscle Society - Granada, Spain, 2016.
  47. Samoes, R; Oliveira, J; Taipa, R; Goncalves, A; Cardoso, M; Coelho, Teresa; Melo Pires, M; Santos, R.; Santos, M.. "Ryanodine-related myopathies: Clinical, histopathologic and genetic heterogeneity among 16 patients from a portuguese tertiary centre". Trabalho apresentado em 21st International Congress of the World Muscle Society - Granada, Spain, 2016.
  48. Ferreira, Natalia; Abreu, Ana Carolina; Carneiro, Ines; Coelho, Teresa; Maria do Carmo Vilas Boas. "Role of gender and onset age as predictors of ophthalmologic changes in Transthyretin Familial Amyloid Polyneuropathy (TTR-FAP) patients". Trabalho apresentado em XVth International Symposium on Amyloidosis - Uppsala, Sweden, 2016.
  49. Ferreira, Natália; Coelho, Joao; Fonseca, Isabel; Vilas-Boas, Maria do Carmo; Coelho, Teresa. "Evolution of ophthalmological alterations in TTR Met30 FAP on Tafamidis". Trabalho apresentado em XVth International Symposium on Amyloidosis - Uppsala, Sweden, 2016.
  50. Ferreira, Natalia; Dias, David; Fonseca, Isabel; Coelho, Teresa. "Specific ocular changes in TTR Met30 FAP after liver transplantation". Trabalho apresentado em 1st European Congress on Hereditary ATTR Amyloidosis - Paris, France, 2015.
  51. Ferreira, Natália; Coelho, Joao; Dias, David; Coelho, Teresa. "Specific ophthalmologic changes in late onset FAP portuguese patients". Trabalho apresentado em 1st European Congress on Hereditary ATTR Amyloidosis - Paris, France, 2015.
  52. Lopes, Alice; Sousa, Alexandra; Fonseca, Isabel; Branco, Margarida; Rodrigues, Carla; Freitas, Paula; Coelho, Teresa. "Life paths of Familial Amiloidotic Polyneuropathy patients. A descriptive study". Trabalho apresentado em 1st European Congress on Hereditary ATTR Amyloidosis - Paris, France, 2015.
  53. Lopes, Alice; Sousa, Alexandra; Frade, Ines; Miranda, Helena; Coelho, Teresa; Daniel,Jorge. "Quality of life and psychosocial aspects in liver transplantation. A longitudinal survey". Trabalho apresentado em 17th Congress of the European Society for Organ Transplantation - Brussels, Belgium, 2015.
  54. Martins, Joana; Moreira, Isabel; Vieira, Emília; Santos, Rosário; Coelho, Teresa. "Descrição de uma família com doença muscular com rippling e fraqueza distal com uma mutação no gene da Caveolina". Trabalho apresentado em Fórum De Neurologia 2015 - Aveiro, Portugal, 2015.
  55. Coelho, Teresa; Monteiro, C; Kristen, A; Benson, M; Karayal, O; Mundayat, R. "Transthyretin Amyloidosis Outcomes Survey (THAOS): Early symptom presentation in Hereditary Transthyretin Amyloidosis". Trabalho apresentado em 13th International Congress on Neuromuscular Diseases - Nice, France, 2014.
  56. Coelho, Teresa; Conceicao, I; Martins da Silva, A; Cardoso, M; Monteiro, C; Alves, C; Pereira, P; Rodrigues, C; Fonseca, I. "Evolution of one-year treatment with Tafamidis in portuguese patients with Transthyretin Familial Amyloid Polyneuropathy". Trabalho apresentado em Joint Congress of European Neurology European Neurological Society and the European Federation of Neurological Societies - Istambul, Turkey, 2014.
  57. Chapman, J; Coelho, Teresa; Kelly, J; Jiang, X. "A quantitative, non-native TTR Elisa Assay for V30M FAP patient identification and use as a biomarker in drug development". Trabalho apresentado em The XIV International Symposium On Amyloidosis - Indiannapolis, USA, 2014.
  58. Ferreira, N.; Coelho, Teresa. "Specific ophtalmologic changes in late onset familial amyloidpolyneuropathy (FAP)". Trabalho apresentado em The XIV International Symposium On Amyloidosis - Indiannapolis, USA, 2014.
  59. Ferreira, N.; Karayal, O; Mundayat, R; Coelho, Teresa. "Ophtalmic findings in THAOS – the Transthyretun Amyloidosis Survey". Trabalho apresentado em XIV International Symposium On Amyloidosis - Indiannapolis, USA, 2014.
  60. Rocha, A; Martins da Silva, A; Cardoso, M; Monteiro, C; Beirão, I; Alves, C; Coelho, Teresa; Lobato, L. "Treatment of ATTR V30M with Tafamidis: Successful decrease of proteinuria". Trabalho apresentado em XIV International Symposium On Amyloidosis, Indiannapolis, 2014.
  61. Alves, C; Vilas-Boas, M; Valdrez, K; Martins da Silva, A; Pessegueiro, H; Daniel, J; Taipa, R; et al. "Domino Liver Transplantation (DLT) and De Novo Familial Amyloid Polyneuropathy (FAP) at Hospital De Santo António/Centro Hospitalar Do Porto (CHP)". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy - Rio de Janeiro, Brasil, 2013.
  62. Alves Ferreira, M; Coelho, Teresa; Santos, D.; Sequeiros, J; Alonso, I; Sousa, A.; Lemos, C. "What does the TTR Locus tell us about the variation in age-at-onset in Familial Amyloid Polyneuropathy?". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy - Rio de Janeiro, 2013.
  63. Santos, D.; Coelho, Teresa; Alves Ferreira, M; Sequeiros, J; Alonso, I; Sousa, A.; Lemos, C. "Study of Apoe polymorphisms as possible modifiers of age-at-onset in Familial Amyloid Polyneuropathy (FAP ATTR V30M)". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy - Rio de Janeiro, Brasil, 2013.
  64. Domingos, J; Coelho, Teresa; Moreira, I; Martins da Silva, A; Alves, C; Rodrigues, C. "Factors Influencing TTR-FAP Mean Time For Diagnosis". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy - Rio de Janeiro, Brasil, 2013.
  65. Monteiro, C; Coelho, Teresa; Waddington Cruz, M; Kristen, A; Karayal, O; Mundayat, R; Stewart, M. "Transthyretin Amyloidosis Outcomes Survey (THAOS): Clinical Presentation of Symptoms Across The Disease Course For Major Genotype Groups". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy - Rio de Janeiro, Brasil, 2013.
  66. Maurer, M; Falk, R; Kristen, A; Damy, T; Rapezzi, C; Planté Bordeneuve, V; Coelho, Teresa; Mundayat, R; Suhr, O. "Differences in Transthyretin Amyloidosis Between the United States and the Rest Of The World: A report from the Transthyretin Amyloid Outcomes Survey (THAOS)". Trabalho apresentado em 17th Annual Meeting Of The Heart Failure Society Of America - Orlando, USA, 2013.
  67. Planté Bordeneuve, V; Coelho, Teresa; Lawson, V; Schumacher, J; Mundayat, R; Karayal, O; Rapezzi, C. "Unravelling Pheno-Genotypic Associations In Transthyretin Amyloidosis Using Data From THAOS – The Transthyretin Amyloidosis Outcome Survey". Trabalho apresentado em 65th Annual Meeting of American Academy of Neurology - San Diego, USA, 2013.
  68. Cardoso, M; Coelho, Teresa; Mundayat, R. "Overview Of Patient Demographics And Clinical Characteristics In THAOS – The Transthyretin Amyloidosis Outcome Survey". Trabalho apresentado em 65th Annual Meeting of American Academy of Neurology - San Diego, USA, 2013.
  69. Lemos, C; Coelho, Teresa; Martins da Silva, A; Sequeiros, J; Sousa, A.. "Age-at-onset variation in a large group of FAP ATTRV30M kindreds: Gender differences and the phenomenon of anticipation". Trabalho apresentado em 16ª Reunião da Sociedade Portuguesa de Genética Humana - Porto, Portugal, 2012.
  70. Rocha, S; Viana Pinheiro; Guimaraes, A; Coelho, Teresa. "Miotonia Congénita: Variabilidade Fenotípica Dominante Ou Recessiva". Trabalho apresentado em Congresso De Neurologia 2012 - Lisboa, Portugal, 2012.
  71. Coelho, Teresa; Santos, D.; Neto, J; Pinto Basto, J; Sequeiros, J; Alonso, I; Lemos, C; Sousa, A.. "The Role of APCS and RBP4 Genes as Modifiers of Age-At-Onset in Familial Amyloid Polyneuropathy (FAP ATTRV30M)". Trabalho apresentado em 62nd Meeting American Society Of Human Genetics - San Francisco, USA, 2012.
  72. Lemos, C; Coelho, Teresa; Martins da Silva, A; Sequeiros, J; Sousa, A.. "Parent-of-origin effects and gender differences influence age-at-onset variation in FAP ATTRV30M kindreds". Trabalho apresentado em Meeting American Society Of Human Genetics - San Francisco, USA, 2012.
  73. Coelho, Teresa; Maurer, M; Matthew, S; Planté Bordeneuve, V; Rapezzi, C; Suhr, O. "Baseline demographics and clinical characteristics in THAOS - The Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em 16th Congress Of The European Federation Of Neurologic Societies - Stockholm, Sweden, 2012.
  74. Coelho, Teresa; Conceicao, I; Planté Bordeneuve, V; Waddington Cruz, M. "Description of Neuropathic Symptoms Reported by ATTR Patients in THAOS – The Transthyretin Amyloidosis Outcome Survey". Trabalho apresentado em 16th Congress Of The European Federation Of Neurologic Societies - Stockholm, Sweden, 2012.
  75. Merlini, G; Coelho, Teresa; Judge, D; Planté Bordeneuve, V; Kelly, J; Lombardo, I. "Transthyretin Stabilization by Tafamidis in Patients With Transthyretin Amyloidosis". Trabalho apresentado em 16th Congress Of The European Federation Of Neurologic Societies - Stockholm, Sweden, 2012.
  76. Santos, D.; Coelho, Teresa; Neto, J; Pinto Basto, J; Sequeiros, J; Alonso, I; Lemos, C; Sousa, A.. "APCS and RBP4 Will Act As Modifiers Of Age-At-Onset In Familial Amyloid Polyneuropathy (FAP ATTRV30M)?". Trabalho apresentado em European Congress of Epidemiology 2012 - Porto, Portugal, 2012.
  77. Lemos, C; Coelho, Teresa; Martins da Silva, A; Sequeiros, J; Mendonça, D; Sousa, A.. "Anticipation Of Age-At-Onset In A Group Of Portuguese Familial Amyloid Polyneuropathy (FAP ATTRV30M) Kindreds". Trabalho apresentado em European Congress of Epidemiology 2012 - Porto, Portugal, 2012.
  78. Sousa, A.; Coelho, Teresa; Lemos, C; Mendonça, D. "The use of survival analysis to estimate age-at-onset of Familial Amyloid Polyneuropathy (FAPATTRV30M) highlights gender differences in early-onset (o.<40) patients but fails to detect it in late-onset (o.>50) patients". Trabalho apresentado em European Human Genetics Conference 2012 - Nuremberg, Germany, 2012.
  79. Santos, D.; Coelho, Teresa; Neto, J; Pinto Basto, J; Sequeiros, J; Alonso, I; Lemos, C; Sousa, A.. "APCS and RBP4: Possible modifiers of age-at-onset in Familial Amyloid Polyneuropathy". Trabalho apresentado em European Human Genetics Conference 2012 - Nuremberg, Germany, 2012.
  80. Lemos, C; Coelho, Teresa; Santos, D.; Neto, J; Alves Ferreira, M; Pinto Basto, J; Sequeiros, J; Alonso, I; Sousa, A.. "Variability In Age-At-Onset Of Familial Amyloid Polyneuropathy (FAP ATTRV30M): An Extended Haplotype Effect?". Trabalho apresentado em European Human Genetics Conference 2012 - Nuremberg, Germany, 2012.
  81. Coelho, Teresa; Maurer, M; Matthew, S; Waddington Cruz M, Et Al.. "Baseline profile of patients undergoing Tafamidis treatment in THAOS – The Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em XIII International Symposium on Amyloidosis - Groningen, The Netherlands, 2012.
  82. Coelho, Teresa; Martins da Silva, A; Lemos, C; Sousa, A.. "Gender Differences And Variability Of Age-Of-Onset In Familial Amyloid Polyneuropathy (ATTRV30M) In Portugal. A Reappraisal". Trabalho apresentado em XIII International Symposium on Amyloidosis, Groningen - The Netherlands, 2012.
  83. Monteiro, C; Sequeira, T; Santos, M.; Martinho, A; Sá, I.; Reis, H; Coelho, Teresa. "Heart Failure Secondary To Severe Cardiomyopathy: Clinical Presentation Of Familial Amyloid Polyneuropathy With Val30Met Mutation". Trabalho apresentado em XIII International Symposium on Amyloidosis - Groningen, The Netherlands, 2012.
  84. Merlini, G; Coelho, Teresa; Falk, R; Judge, D; Lombardo, I. "Transthyretin Stabilization, Efficacy And Safety Of Tafamidis For The Treatment Of Transthyretin Amyloidosis". Trabalho apresentado em XIII International Symposium on Amyloidosis - Groningen, The Netherlands, 2012.
  85. Lemos, C; Coelho, Teresa; Martins da Silva, A; Sequeiros, J; Sousa, A.. "Anticipation Is A True Biological Mechanism Observed In A Large Group Of Portuguese FAP ATTRV30M Kindreds". Trabalho apresentado em XIII International Symposium on Amyloidosis - Groningen, The Netherlands, 2012.
  86. Coelho, Teresa; Maurer, M; Planté-Bordeneuve, V; Rapezzi C, Et Al. "Baseline demographics in THAOS - the Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em 64th Annual Meeting of American Academy of Neurology - New Orleans, USA, 2012.
  87. Kaufman, H; Maurer, M; Coelho, Teresa; Planté-Bordeneuve, V; Rapezzi, C; Suhr, O Et Al.. "Comparison of US and non-US patients with Familial Amyloid Polyneuropathy (FAP) and Familial Amyloid Cardiomyopathy (FAC) in THAOS". Trabalho apresentado em 64th Annual Meeting of American Academy of Neurology - New Orleans, USA, 2012.
  88. Sousa, A.; Lemos, C; Martins da Silva, A; Neto, J; Alonso, I; Pinto Basto, J; Sequeiros, J; Coelho, Teresa. "Familial Amyloid Polyneuropathy Attrv30m: What Can We Learn From The Study Of Families In Which The Proband Had No Affected Parent At The Time Of Diagnosis". Trabalho apresentado em 12th Meeting International Congress Of Human Genetics/61st Meeting American Society Of Human Genetics - Montréal, Canada, 2011.
  89. Lemos, C; Coelho, Teresa; Neto, J; Pinto Basto, J; Sequeiros, J; Alonso, I; Sousa, A.. "The Role Of CIS-Acting Genetic Modifiers In Phenotypic Variability Of Familial Amyloid Polyneuropathy ATTRV30M". Trabalho apresentado em 12th Meeting International Congress Of Human Genetics/61st Meeting American Society Of Human Genetics - Montréal, Canada, 2011.
  90. Santos, D.; Coelho, Teresa; Neto, J; Pinto Basto, J; Sequeiros, J; Alonso, I; Lemos, C; Sousa, A.. "Searching For Modifiers Of Age-At-Onset In Familial Amyloid Polyneuropathy (FAP) ATTRV30M: A Candidate Gene Approach". Trabalho apresentado em 12th Meeting International Congress Of Human Genetics/61st Meeting American Society Of Human Genetics - Montréal, Canada, 2011.
  91. Coelho, Teresa; Maia, L; Martins da Silva, A; Waddington Cruz, M; Planté-Bordeneuve, V; Lozeron, P; Suhr, O; et al. "Tafamidis And Nerve Fiber Function In Transthyretin-Type Familial Amyloid Polyneuropathy". Trabalho apresentado em American Association of Neuromuscular & Electrodiagnostic Medicine Annual Meeting 2011 - San Francisco, USA, 2011.
  92. Coelho, Teresa; Waddington-Cruz, M; Conceicao, I; Planté-Bordeneuve, V; Ericzon, B; Falk, R; Ikeda, S; et al. "Baseline Nutritional Status In The Transthyretin Amyloidosis Outcome Survey (THAOS)". Trabalho apresentado em 15th Congress of The European Federation of Neurological Societies - Budapest, Turkey, 2011.
  93. Waddington Cruz, M; Coelho, Teresa; Conceicao, I; Planté-Bordeneuve, V; Ericzon, B; Falk, R; Ikeda, S; et al. "Demographics And Neurologic Function In Early- And Late-Onset Syptomatic Patients In The Transthyretin Amyloidosis Outcomes Survey (THAOS)". Trabalho apresentado em 2011 Meeting of the Peripheral Nerve Society - Potomac, USA, 2011.
  94. Vinik, E; Vinik, A; Paulson, J; Merkies, I; Coelho, Teresa; Grogan, D. "Validation Of Norfolk QOL-DN As A Measure Of Qol In Patients With Transthyretin Familial Amyloid Polyneuropathy". Trabalho apresentado em 2011 Meeting of the Peripheral Nerve Society - Potomac, USA, 2011.
  95. Coelho, Teresa; Sousa, Alda. "Familial Amyloid Polyneuropathy (Fap Attrv30m): A Good Model For Genetic Modifiers For Age-At-Onset". Trabalho apresentado em 21st Meeting Of The European Neurological Society - Lisbon, Portugal, 2011.
  96. Reguengo, H; Cardoso, M; Coelho, Teresa; Martins da Silva, A; Novais, M; Gomes, L; Fonseca, I; Martins, B; Marques, F. "SOD Levels On Erythrocytes From FAP Patients Show Increased Oxidative Stress". Trabalho apresentado em 21st International Congress Of Clinical Chemistry And Laboratory Medicine - Berlin, Germany, 2011.
  97. Lemos, C; Coelho, Teresa; Neto, J; Pinto Basto, J; Sequeiros, J; Alonso, I; Sousa, A. "Can Variability Of Age-At-Onset In Familial Amyloid Polyneuropathy ATTRV30M Be Explained By CIS-Acting Genetic Modifiers?". Trabalho apresentado em 2nd I3s Retreat - Póvoa De Varzim, Portugal, 2011.
  98. Coelho, Teresa; Maia, L; Martins da Silva, A; Waddington Cruz, M; Planté-Bordeneuve, V; Lozeron, P; Suhr, O; Campistol J, Conceição I, Schmidt H, Trigo P, Packman J, Grogan D. "A Comprehensive Evaluation Of The Disease-Modifying Effects Of Tafamidis In Patients With Transthyretin Type Familial Amyloid Polyneuropathy". Trabalho apresentado em 63rd American Academy of Neurology OMeeting - Honolulu, USA, 2011.
  99. Conceição, I; Coelho, Teresa; Planté-Bordeneuve, V; Waddington Cruz, M; Ericzon, B; Falk, R; Ikeda, S; Mauer M, Suhr O B, Ando Y, Mazzeo A, Grogan D. "Baseline Neurologic Function In Symptomatic Patients In The Transthyretin Amyloidosis Outcomes Survey (THAOS)". Trabalho apresentado em 63rd American Academy of Neurology Meeting - Honolulu, USA, 2011.
  100. Coelho, Teresa; Merkies, I; Vinik, A; Vinik, E; Chan, J; Packman, J; Grogan, D. "Relationship Between Objective Measures Of Neuropathy And Quality Of Life In Stages Of Severity Of Transthyretin Familial Amyloid Polyneuropathy". Trabalho apresentado em XII International Symposium on Amyloidosis - Rome, Italy, 2010.
  101. Planté-Bordeneuve, V; Coelho, Teresa; Ericzon, B; Falk, R; Ikeda, S; Mauer, M; Suhr, O; Trigo, P; Grogan, D. "Initial Findings From The Transthyretin Amyloidosis Outcomes Survey (THAOS) – A Global Web-Based Registry". Trabalho apresentado em 62nd American Academy of Neurology Meeting - Toronto, Canada, 2010.
  102. Coelho, Teresa; Maia, L; Cavaco, S; Melo Pires, M; Freitas, J; Dias, D; Miranda, H; Magalhães, R; Correia, M. "Post-Liver Transplant ATTR Val30Met Patients: CNS Clinical Phenotype". Trabalho apresentado em 62nd American Academy of Neurology Meeting - Toronto, Canada, 2010.
  103. Coelho, Teresa; Merkies, I; Vinik, A; Vinik, E; Chan, J; Packman, J; Grogan, D. "Outcome Measures For Transthyretin Type Familial Amyloid Polyneuropathy". Trabalho apresentado em 62nd American Academy of Neurology Meeting - Toronto, Canada, 2010.
  104. Coelho, Teresa; Maia, L; Martins da Silva, A; Waddington-Cruz, M; Planté-Bordeneuve, V; Suhr, O; Campistol J, Conceiçao I, Schmidt H, Trigo P, Grogan D, Packman J. "A Landmark Clinical Trial Of A Novel Small Molecule Transthyretin Stabilizer, Fx-1006a, In Patients With TTR Amyloid Polyneuropathy: A Phase II/III, Randomized, Double-Blind, Placebo-Controlled Study". Trabalho apresentado em Peripheral Nerve Society Meeting 2009 - Würzburg, Germany, 2009.
  105. Planté-Bordeneuve, V; Coelho, Teresa; Ericzon, B; Falk, R; Ikeda, M; Maurer, M; Suhr, O; Trigo, P; Grogan, D. "THAOS. Transthyretin Amyloidosis Outcomes Survey, A New Global Web-Based Registry". Trabalho apresentado em Peripheral Nerve Society Meeting 2009 - Würzburg, Germany, 2009.
  106. Coelho, Teresa; Maia, L; Martins da Silva, A; Waddington-Cruz, M; Planté-Bordeneuve, V; Suhr, O; Campistol, J; et al. "A Landmark Clinical Trial Of A Novel Small Molecule Transthyretin Stabilizer, Fx-1006a, In Patients With TTR Amyloid Polyneuropathy: A Phase II/III, Randomized, Double-Blind, Placebo-Controlled Study". Trabalho apresentado em 61st American Academy of Neurology Meeting - Seattle, USA, 2009.
  107. Planté-Bordeneuve, V; Coelho, Teresa; Ericzon, B; Falk, R; Ikeda, S; Maurer, M; Suhr, O; Trigo, P; Grogan, D. "THAOS. Transthyretin Amyloidosis Outcomes Survey, A New Global, Web-Based Registry". Trabalho apresentado em 61st American Academy of Neurology Meeting - Seattle, USA, 2009.
  108. Felgueiras, R; Damásio, J; Coelho, Teresa. "Revisão Genética E Clínica De 30 Doentes Com Distrofia Facioescapulohumeral". Trabalho apresentado em Congresso De Neurologia 2008 - Porto, Portugal, 2008.
  109. Coelho, Teresa; Maia, L; Waddington-Cruz, M; Martins da Silva, A; Planté-Bordeneuve, V; Suhr, O; Campistol J, Conceição I, Schmidt H, Trigo P, Cros D, Grogan D, Packman J. "Apresentação de um ensaio clínico com uma molécula estabilizadora da Transtirretina em doentes com Polineuropatia Amiloidótica Familiar". Trabalho apresentado em Congresso De Neurologia 2008 - Porto, Portugal, 2008.
  110. Santos, M.; Coelho, Teresa; Lima, J; Mihaylova, V; Muller, J; Lochmuller, H. "Congenital Myasthenic Syndromes – Eight Northern Portuguese Patients". Trabalho apresentado em 13th International Congress Of The World Muscle Society. Newcastle, England, 2008.
  111. Cardoso, M; Santos, E.; Carvalho, A; Coelho, Teresa. "Endocrine and Metabolic Disorders in Myothonic Dystrophy Type 1". Trabalho apresentado em 13th International Congress of The World Muscle Society - Newcastle, England, 2008.
  112. Coelho, Teresa; Maia, L; Martins da Silva, A; Waddington-Cruz, M; Planté-Bordeneuve, V; Suhr O, Campistol J, Conceição I, Schmidt H, Trigo P, Cros D, Grogan D, Packman J. "A Landmark Clinical Trial Of A Novel Small Molecule Transthyretin Stabilizer, Fx-1006a, In Patients With TTR Amyloid Polyneuropathy. A Phase II/III, Randomized, Double-Blind, Placebo-Controlled Study". Trabalho apresentado em VII International Symposium on Familial Amyloid Polyneuropathy and 1st International Workshop on Hereditary Amyloidosis, London, England, 2008.
  113. Planté-Bordeneuve, V; Suhr, O; Coelho, Teresa; Ericzon, B; Labaudinière, R; Packman, J; Grogan, D. "THAOS - Transthyretin Amyloidoses Outcomes Survey, A New Global, Web-Based Registry". Trabalho apresentado em VII International Symposium on Familial Amyloid Polyneuropathy and 1st International Workshop on Hereditary Amyloidosis, London, England, 2008.
  114. Maia, L; Coelho, Teresa; Melo Pires, M; Saraiva, M; Guimaraes, A. "Different Patterns of CNS TTR Amyloid Pathology". Trabalho apresentado em VII International Symposium on Familial Amyloid Polyneuropathy and 1st International Workshop on Hereditary Amyloidosis, London, England, 2008.
  115. Planté-Bordeneuve, V; Suhr, O; Coelho, Teresa; Labaudinière, R; Packman, J; Grogan, D. "THAOS - Transthyretin Amyloidoses Outcomes Survey, A New Global, Web-Based Registry". Trabalho apresentado em 18th Meeting of The European Neurological Society, Nice, France, 2008.
  116. Coelho, Teresa; Waddington-Cruz, M; Planté-Bordeneuve, V; Cros, D; Grogan, D; Packman, J. "Correlation Of Clinical Outcomes And Disease Burden In Patients With Transthyretin (TTR) Amyloid Polyneuropathy: Study Fx-005, A Landmark Clinical Trial Of Fx-1006a, A Novel Small Molecule TTR Stabiliser". Trabalho apresentado em 18th Meeting of The European Neurological Society - Nice, France, 2008.
  117. Waddington-Cruz, M; Coelho, Teresa; Maia, L; Martins da Silva, A; Planté-Bordeneuve, V; Suhr, O; Campistol, J; et al. "A Landmark Clinical Trial Of A Novel Small Molecule Transthyretin (TTR) Stabiliser, Fx-1006a, In Patients With TTR Amyloid Polyneuropathy: A Phase II/III, Randomised, Double-Blind, Placebo-Controlled Study". Trabalho apresentado em 18th Meeting of The European Neurological Society - Nice, France, 2008.
  118. Taipa, R; Coelho, Teresa; Melo Pires, M; Moreira, T; Correia, C. "CIDP Associated With Hepatitis C Virus Infection Responsive To Combination Antiviral Therapy". Trabalho apresentado em 18th Meeting of The European Neurological Society - Nice, France, 2008.
  119. Cardoso, M; Santos, E.; Ramalheira, J; Lopes, J; Coelho, Teresa. "Sleep Disorders In Myotonic Dystrophy Type 1". Trabalho apresentado em 18th Meeting of The European Neurological Society - Nice, France, 2008.
  120. Coelho, Teresa. "Safety And Efficacy Of Oral-Administered Fx-1006a In Patients With Familial Amyloid Polyneuropathy (FAP): A Phase II/III, Randomized, Double-Blind, Placebo-Controlled Study". Trabalho apresentado em 4th European Conference on Rare Diseases - Lisboa, Portugal, 2007.
  121. Barbas do Amaral, J; Coelho, Teresa; Guimaraes, A. "Labial Salivary Gland Biopsy For Fap Diagnosis". Trabalho apresentado em XIst International Symposium on Amyloidosis - Woods Hole, USA, 2006.
  122. Bulawa, C; Wang, L; Coelho, Teresa; Ranløv, P; Svendsen, I; Packman, J; Labaudinière, R. "Stabilization Of Amyloidgenic Transthyretin Variants In Plasma By Fx-1006a". Trabalho apresentado em XIst International Symposium on Amyloidosis - Woods Hole, USA, 2006.
  123. Coelho, Teresa; Martins da Silva, A; Maia, L; Sousa, A.. "Genetic Epidemiology of FAP In Portugal". Trabalho apresentado em XIst International Symposium on Amyloidosis - Woods Hole, USA, 2006.
  124. Lopes, A; Carvalho, I.; Seca, R; Pessegueiro, H; Coelho, Teresa; Pereira, R.; Teixeira, M; Ribeiro, V; Amil, M. "Quality Of Life 10 Years Of Liver Transplantation". Trabalho apresentado em XIst International Symposium on Amyloidosis - Woods Hole, USA, 2006.
  125. Coelho, Teresa; Santos, M.; Cerqueira, R; Melo Pires, M; Lameiras, L; Gabriel, H; Fernandes, A; Tavares, P; Guimarães, A. "Three Novel Mutations of The Myelin P0 Gene (MPZ) in Portuguese Families With CMT1b". Trabalho apresentado em 11th International Congress of The World Muscle Society - Bruges, Belgium, 2006.
  126. Santos, M.; Coelho, Teresa; Machado, A; Cerqueira, R; Fernandes, A; Tavares, P. "Hereditary Neuropathies in a Pediatric Clinic". Trabalho apresentado em 11th International Congress of the World Muscle Society - Bruges, Belgium, 2006.
  127. Magalhães, P; Silveira, I; Coelho, Teresa; Sequeiros, J. "Frequency o f 17p11.2 Duplication/Deletion in a Group of Portuguese Patients with Charcot-Marie-Tooth Type 1 (CMT1a) and Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)”.". Trabalho apresentado em European Human Genetics Conference 2006 - Amsterdam, The Netherlands, 2006.
  128. Coelho, Teresa; Cerqueira, R; Lameiras, L; Gabriel, H; Santos, M.; Tavares, P; Fernandes, A. "Novel Mutation of the Myelin P0 Gene (MPZ) in a Portuguese Family with CMT1b Disease". Trabalho apresentado em European Human Genetics Conference 2006 - Amsterdam, The Netherlands, 2006.
  129. Pinto Basto, J; Coelho, Teresa; Leal Loureiro, J; Rocha, J; Lopes, A; Sequeiros, J. "Prenatal Diagnosis In Late Onset Neurological Disorders In Portugal. Experience With 83 Requests Since 1996". Trabalho apresentado em European Human Genetics Conference 2006 - Amsterdam, The Netherlands, 2006.
  130. Rolim, L; Lopes, A; Rodrigues, C; Coelho, Teresa. "Estudo de Validação da Escala de Avaliação da Coesão e da Adaptabilidade Familiares – III (Faces III) numa Amostra Portuguesa de Doentes com Polineuropatia Amiloidótica Familiar". Trabalho apresentado em 6.º Congresso Nacional de Psicologia da Saúde - Faro, Portugal, 2006.
  131. Vila-Chã, N; Maia, L; Melo Pires, M; Coelho, Teresa; Magalhães, M; Lopes Lima, J. "Pakinsonismo e Dropped Head Syndrome". Trabalho apresentado em Congresso de Neurologia 2004 - Espinho, Portugal, 2004.
  132. Chaves, J; Fonseca, I; Lobato, L; Reis, H; Coelho, Teresa. "Cardiomyopathy in Familial Amyloid Polyneuropathy". Trabalho apresentado em Congress of the European Federation of Neurological Societies - Paris, France, 2004.
  133. Maré, R; Coelho, Teresa; Santos, R.; Santos, M.. "Estudo Clínico e Molecular de 39 Doentes com Atrofia Espinal Progressiva". Trabalho apresentado em Congresso de Neurologia 2002 - Espinho, Portugal, 2002.
  134. Marta, M; Martins da Silva, A; Silva, AP; Meireles, L; Coelho, Teresa; Leite, I. "Hearing Loss in 17 Patients with Mitochondrial Disorders". Trabalho apresentado em Xth International Congress on Neuromuscular Diseases - Vancouver, Canada, 2002.
  135. Maré, R; Tuna, A; Santos, M.; Coelho, Teresa. "Distal Hereditary Motor Neuropathy. Two Portuguese Families.". Trabalho apresentado em Xth International Congress On Neuromuscular Diseases - Vancouver, Canada, 2002.
  136. Coelho, Teresa; Tuna, A; Marta, M; Martins da Silva, A; Fraga, C; Sousa, A.. "Do Familial Amyloid Polyneuropathy Patients Live Longer After Liver Transplantion?". Trabalho apresentado em Xth International Congress On Neuromuscular Diseases - Vancouver, Canada, 2002.
  137. Martins da Silva, A; Lemos, J; Brito, R.; Leite, I; Paiva, I; Lopes, J; Correia, M; et al. "Evoked Potentials in Chronic Idiopathic Inflammatory Demyelinating Polyneuropathy". Trabalho apresentado em Xth International Congress On Neuromuscular Diseases - Vancouver, Canada, 2002.
  138. Marta, M; Coelho, Teresa; Guimarães, A; Santos, M.; Guimaraes, A. "Autossomal Recessive Centronuclear Myopathy: Clinical and Muscle Biopsy Characteristics of Three Patients". Trabalho apresentado em Xth International Congress On Neuromuscular Diseases - Vancouver, Canada, 2002.
  139. Marta, M; Palmares, M; Sousa, A.; Coelho, Teresa. "Advantages Of Facioscapulohumeral Muscular Dystrophy Molecular Diagnosis: Experience With 13 Families From The North Of Portugal". Trabalho apresentado em Xth International Congress on Neuromuscular Diseases - Vancouver, Canada, 2002.
  140. Mendes, P; Meneses, I; Ramos, H; Coelho, Teresa; Vasconcelos, C; Lemos, M; Ferreira, R.; Miranda, M; Monteiro, L. "Evolução Fenotípica na Adrenoleucodistrofia". Trabalho apresentado em Congresso Português de Neurologia 2001 - Lisboa, Portugal, 2001.
  141. Marta, M; Palmares, M; Sousa, A; Coelho, Teresa. "Importância Do Diagnóstico Molecular no Estudo dos Doentes Com Distrofia Facioescapulohumeral: Resultados de 12 Famílias do Norte De Portugal". Trabalho apresentado em Congresso Português de Neurologia 2001 - Lisboa, Portugal, 2001.
  142. Marta, M; Coelho, Teresa; Guimarães, A; Santos, M.. "Miopatia Centronuclear Autossómica Recessiva: Descrição das Características Clínicas e Histopatológicas de Três Doentes". Trabalho apresentado em Congresso Português de Neurologia 2001 - Lisboa, Portugal, 2001.
  143. Sousa, A; Martins da Silva, A; Marta, M; Sequeiros, J; Coelho, Teresa. "Familial Amyloid Neuropathy (FAP Met30) in Portugal: A Combined Use of Family Studies and A 60 Years’ Register in the Assessment of Anticipation Of Age-At- Onset and the Evolutionary Dynamics of the Gene". Trabalho apresentado em 51st Meeting American Society Of Human Genetics - San Diego, USA, 2001.
  144. Marta, M; Martins da Silva, A; Sousa, A; Coelho, Teresa. "Familial Amyloid Polyneuropathy In Portugal: A Disease In Expansion With Variable Clinical Characteristics". Trabalho apresentado em XVII World Congress of Neurology - London, England, 2001.
  145. Martins da Silva, A; Marta, M; Sousa, A; Coelho, Teresa. "Familial Amyloid Polyneuropathy in Portugal is a Disease in Expansion With Variable Age of Onset". Trabalho apresentado em 53rd Annual Meeting of the American Academy of Neurology - Philadelphia, USA, 2001.
  146. Maré, R; Coelho, Teresa; Santos, R.; Santos, M.. "Atrofia Espinal Progressiva. Estudo Clínico e Molecular". Trabalho apresentado em Reunião Anual da Sociedade Portuguesa de Genética Humana - Porto, Portugal, 2000.
Resumo em conferência
  1. Carmo Vilas-Boas, Maria do; Patricia Rocha, Ana; Pereira Choupina, Hugo Miguel; Cardoso, Marcio; Fernandes, Jose Maria; Coelho, Teresa; Silva Cunha, Joao Paulo. "TTR-FAP Progression Evaluation Based on Gait Analysis Using a Single RGB-D Camera". Trabalho apresentado em 41st Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), Berlin, 2019.
    Publicado • 10.1109/embc.2019.8857354
  2. Renata Souto Silva; Vanessa Oliveira; Ana Paula Sousa; Cristina Garrido; Coelho, Teresa; Manuela Santos. "Atrofia Muscular Espinhal Tipos 1 a 4 - Caracterização dos doentes do Centro Hospitalar do Porto". Trabalho apresentado em Congresso de Neurologia 2018, Porto, 2018.
    Publicado
  3. Fernandes, A; Coelho, Teresa; Rodrigues, A; Felgueiras, H; Oliveira, P; Guimaraes, A; Melo Pires, M; Taipa, R. "Correlações Clinico-Patológicas Nas Biopsias De Nervo Sural Na Polineuropatia Amiloidótica Familiar Por Transtirretina". Trabalho apresentado em Sinapse 18 supl Nº2 - Congresso de Neurologia 2018 (SPN), Porto, 2018.
    Publicado
  4. Oliveira Santos, M; Falcao de Campos, C; Garrido, C; Conceicao, I; Palavra, F; Negrao, L; Vieira, JP; et al. "Clinical and Molecular Features of Proximal Spinal Muscle Atrophy in Portugal: A Multicentre Retrospective Study". Trabalho apresentado em Neuromuscular Disorders - 23rd International Annual Congress of the World Muscle Society, Mendoza, 2018.
    Publicado
  5. Sousa, A; Valdrez, K; Anselmo, J; Cardoso, Marcio; Coelho, Teresa. "Comparison of Sudoscan, Qsart and SSR in the evaluation of sudomotor dysfunction". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  6. Monteiro, C; Martins da Silva, A.; Rodrigues, C; Anselmo, J; Fernandes, J; Coelho, Teresa. "Development and validation of the Transthyretin Familial Amyloid Polyneuropapathy Score (TTR-FAP Score)". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  7. Dick, P; Wang, A; Coelho, Teresa; Cruz, MW; Polydefkis, M; Gertz, M; Sheinberg, M; et al. "Inotersen improved quality of life and neuropathy measures across levels of Transthyretin reduction (Neuro-TTR)". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  8. Brannagan, T; Wang, A; Coelho, Teresa; Cruz, MW; Polydefkis, M; Dyck, P; Plantebordeneuve, V; et al. "Open-Label extension of the Neuro-TTR study in patients with Hereditary Transthyretin (Hattr) Amyloidosis: Long-Term update". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  9. Coelho, Teresa; Ebenezer G; Sousa, AP; Wagner, K; Alves, C; Zhou, Y; Cardoso, M; Polydefkis, M. "Identifying the transition from TTR carrier To TTR neuropathy patient". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  10. Coelho, Teresa; Polydefkis, M; Lin, H; Gollob, J; Agarwal, S; Betts, M; Fahrbach, K; Chitnis, M; Plantebordeneuve, V. "Indirect comparision of Patisiran and Tafamidis for treatment of Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Polyneuropathy". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  11. Dyck, PJ; Adams, D; Polydefkis, M; Coelho, Teresa; Duarte, AG; Kristen, A; Berk, JL; et al. "Neuropathy progression in patients with hATTR Amyloidosis: Analysis of the Apollo placebo arm". Trabalho apresentado em Journal Of The Peripheral Nervous System - Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  12. Polydefkis, M; Coelho, Teresa; Adams, D; Kristen, A; Duarte, AG; Berk, J; Quan, D; et al. "Infusion related reactions in patients with hATTR Amyloidosis treated with Patisiran". Trabalho apresentado em Journal Of The Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  13. Coelho, Teresa; Suhr, O; Quan, D; Brannagan, T; Gollob, J; Goyal, S; Altincatal, A; et al. "Longitudinal changes in MNIS 7 are associated with changes in ambulatory status in Hereditary Transthyretin Mediated Amyloidosis". Trabalho apresentado em Journal Of The Peripheral Nervous System -2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  14. Coelho, Teresa; Flynn, A; Ebede, B; Rill, D; Sultan, M; Li, Huihua; Huber, P. "Comprehensive safety profile of Tafamidis". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  15. David Adams; William Oriordan; Chih Chao Yang; Taro Yamashita; Arnt Kristen; Ivaylo Tournev; Coelho, Teresa; et al. "Changes in neuropathy stage in patients with hATTR Amyloidosis following Patisiran treatment with Patisiran: Analysis from Apollo". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  16. Morie Gertz; Annabel Wang; Coelho, Teresa; Marcia Waddington Cruz; Michael Polydefkis; Peter Dyck; Morton Scheinberg; et al. "Safety and efficacy of Inotersen in patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy (Neuro-TTR)". Trabalho apresentado em Journal of the Peripheral Nervous System - 2018 Peripheral Nerve Society Annual Meeting, Baltimore, Maryland, 2018.
    Publicado
  17. Luisa Sousa; Ernestina Santos; J. Martins; Ana Sousa; Marcio Cardoso; Fernando Silveira; Ricardo Mar; et al. "Congenital myasthenic syndromes in a subpopulation of the north of portugal". Trabalho apresentado em Journal of Neuromuscular Diseases - 15th International Congress on Neuromuscular Diseases, Vienna, Austria, 2018.
    Publicado
  18. Laura Obici; Coelho, Teresa; David Adams; Alejandra Gonzalez Duarte; William Oriordan; Chihchao Yang; Arnt Kristen; et al. "Apollo Phase 3 Study: Impact of baseline neuropathy severity on response to Patisiran". Trabalho apresentado em Journal of Neuromuscular Diseases - 15th International Congress on Neuromuscular Diseases, Vienna, 2018.
    Publicado
  19. Coelho, Teresa; David Adams, Alejandra Gonzalezduarte, William Oriordan, Chihchao Yang, Michael Polydefkis,; Ivaylo Tournev, Hartmut Schmidt, John Berk, Kon Ping Lin, Pritesh Gandhi, Marianne Sweetser, Christine Powell,; Ole Suhr. "Transthyretin reduction with patisiran in the Apollo Phase 3 study". Trabalho apresentado em Journal of Neuromuscular Diseases - 15th International Congress on Neuromuscular Diseases, Vienna, 2018.
    Publicado
  20. Michelle Mauermann; David Adams; Alejandra Gonzalez Duarte; Coelho, Teresa; Chihchao Yang, Michael Polydefkis, Arnt KriArnt Kristen, Ivaylo Tournev, Hartmut Schmidt, John Berk, Kon Ping Lin; Pritesh Gandhi, Marianne Sweetser, Matthew White, Jared Gollob, Ole Suhr. "Impact of Patisiran on Autonomic Neuropathy in Hereditary Transthyretin Mediated Amyloidosis patients". Trabalho apresentado em Journal of Neuromuscular Diseases - 15th International Congress on Neuromuscular Diseases, Vienna, 2018.
    Publicado
  21. Isabel Conceicao; John Berk; Annabel Wang; Coelho, Teresa; M Waddington Cruz, M Polydefkis, P Dyck, M Scheinberg, V Plantebordeneuve, F Barroso, D Adams, T Brannagan, C Whelan; B Drachman, S Heitner, H Schmidt, G Vita, J Campistol, P Gorevic, A Souza Bulle Oliveira, B Monia; A Sikora Kessler, M Gertz, M Benson, G Merlini. "Baseline characteristics of patients with Hereditary Transthyretin (hATTR) Amyloidosis with Polyneuropathy enrolled in the Phase 3 Study Neuro-TTR demonstrate significant disease burden". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  22. S Cavaco; A Martins da Silva; J Fernandes; R Samoes; C Alves; M Cardoso; J Kelly; C Monteiro; Coelho, Teresa. "Age-dependent cognitive dysfunction in untreated and liver transplanted ATTR v30M patients". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  23. Coelho, Teresa; D Adams; A Gonzalez Duarte; W Oriordan; C Yang, T Yamashita, A Kristen, I Tournev, H Schmidt, J Berk, Kp Lin, P Gandhi, M Sweetser; M White, S Goyal, J Gollob, O Suhr. "Outcomes of patients with Hereditary Transthyretin-Mediated Amyloidosis with early onset V30M versus all other mutations in Apollo, A Phase 3 Study of Patisiran". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  24. C Rapezzi; Coelho, Teresa. "Developing a framework to optimise the ongoing assessment of ATTR- Amyloidosis in patients with a cardiac phenotype". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  25. Y Parman; Coelho, Teresa; I Conceicao; L Galn; L Obici; A Rousseau. "Developing a framework to optimise the ongoing assessment of ATTR- Amyloidosis". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  26. C Monteiro; C Rodrigues; J Fernandes; M Cardoso; C Alves; A Martins da Silva; Coelho, Teresa. "Validity and reliability of the Transthyretin Amyloidosis Neuropathy Score (TTRANS), a new outcome measure designed specifically for Familial Amyloid Polyneuropathy (TTR-FAP)". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  27. V Plantebordeneuve; M Waddington Cruz, M Polydefkis, P Dyck, M Scheinberg, J Berk, F Barroso, D Adams, C Whelan, G Merlini, B Drachman,; Coelho, Teresa; S Heitner, I Conceicao, H Schmidt, G Vita, J Campistol, J Gamez, P Gorevic, B Monia, M Benson, M Gertz. "Long-term efficacy and safety of Inotersen in patients with Hereditary Transthyretin (hATTR) Amyloidosis treated in the open label extension of the Phase 3 Study Neuro-TTR". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  28. Coelho, Teresa; D Adams; A Gonzalez Duarte; W Oriordan; CC Yang, T Yamashita, A Kristen, I Tournev, H Schmidt, J Berk, Kp Lin, P Gandhi, M Sweetser; J Chen, S Goyal, J Gollob, O Suhr. "Impact of prior TTR stabilizer use in patients with Hereditary Transthyretin Mediated Amyloidosis in the Apollo Phase 3 Study of Patisiran". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  29. L Obici; Coelho, Teresa; D Adams; A Gonzalez Duarte, W Oriordan, CC Yang, T Yamashita, A Kristen, I Tournev, H Schmidt, J Berk; KP Lin, P Gandhi, M Sweetser, J Chen, S Goyal, J Gollob, O Suhr. "Impact of Patisiran, an investigational RNAi therapeutic, on nutritional status in patients with Hereditary Transthyretin Mediated Amyloidosis". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  30. Coelho, Teresa; A Wang; M Waddington Cruz; M Polydefkis, P Dyck, M Scheinberg, V Plantebordeneuve, J Berk, F Barroso, D Adams; T Brannagan, C Whelan, G Merlini, B Drachman, S Heitner, I Conceicao, H Schmidt, G Vita, J Gamez, E Gane, P Gorevic; A Souza Bulle Oliveira, B Monia, M Gertz, M Benson. "Inotersen improves quality of life and neuropathy in patients with Hereditary Transthyretin (hATTR) Amyloidosis with Polyneuropathy: Results of the Phase 3 Study Neuro-TTR". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  31. Coelho, Teresa. "Sixty years of transthyretin Familial Amyloid Polyneuropathy in Europe: Epidemiology, clinical presentation and genetic basics". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  32. G Vita; M Polydefkis; Coelho, Teresa; M Waddington Cruz, P Dyck, M Scheinberg, V Plantebordeneuve, J Berk, F Barroso, D Adams; T Brannagan, C Whelan, G Merlini, B Drachman, S Heitner, I Conceicao, H Schmidt, J Campistol, E Gane, P Gorevic; A Souze Bulle Oliveira, B Monia, M Gertz, M Benson, A Wang. "Inotersen improved Norfolk Quality Of Life-Diabetic Neuropathy (Norfolk QOLDN) measures in patients with Hereditary Transthyretin (hATTR) Amyloidosis Treated in the Phase 3 Study Neuro-TTR". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, 2018.
    Publicado
  33. L Maia; J Beirao; R Magalhaes; A Carneiro; AC Abreu; H Doria; T Rodrigues; M Correia; Coelho, Teresa. "Impact of central nervous system and ocular phenotypes in ATTR V30M patients". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  34. L Obici; Coelho, Teresa; D Adams; A Gonzalez Duarte, W Oriordan, CC Yang, T Yamashita, A Kristen, I Tournev, H Schmidt, J Berk; KP Lin, P Gandhi, M Sweetser, J Chen, S Goyal, J Gollob, O Suhr. "Impact of Patisiran on Norfolk Quality of Life Questionnaire Diabetic Neuropathy (QOL-DN) in patients with Hereditary Transthyretin-Mediated Amyloidosis: Results from the Phase 3 Apollo Study". Trabalho apresentado em European Journal of Neurology - 4th Congress Of The European Academy Of Neurology, Lisboa, 2018.
    Publicado
  35. Fernandes, Armindo; Coelho, Teresa; Rodrigues, Aurora; Felgueiras, Helena; Oliveira, Pedro; Guimarães, António; Melo Pires, Manuel. "Correlacoes clinico-patologicas nas biopsias de Nervo Sural na Polineuropatia Amiloidótica Familiar por Transtirretina". Trabalho apresentado em Congresso de Neurologia 2018, Porto, 2017.
    Publicado
  36. Vilas-Boas, Maria Do Carmo; Rocha, Ana Patricia; Choupina, Hugo Miguel Pereira; Fernandes, Jose Maria; Coelho, Teresa; Cunha, Joao Paulo Silva. "The first Transthyretin Familial Amyloid Polyneuropathy gait quantification study - preliminary results". Trabalho apresentado em 39th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC'17), Jeju Island, 2017.
    Publicado • 10.1109/embc.2017.8037087
  37. Salgado, Paula; Alves, Cristina; Fonseca, Isabel; Martins da Silva, Ana; Cardoso, Márcio; Valdrez K, Ferreira H, Pessegueiro H, Daniel J, Ferreira S, Gandarra J, Lopes V, Barbas Amaral J, Moreira R; Taipa R, Guimaraes A, Pires MM; Coelho, Teresa. "Transplante hepático sequencial e Polineuropatia Amiloidótica Familiar Adquirida - Experiência do Hospital Santo António/Centro Hospitalar do Porto". Trabalho apresentado em Congresso de Neurologia 2017 - Sinapse 17, Lisboa, 2017.
    Publicado
  38. J Oliveira; M Cardoso; R Taipa; A Goncalves; M Oliveira; M Melo Pires; M.Santos; Coelho, Teresa; R.Santos. "The expanding phenotype of LAMA2-Related muscular dystrophies: Four additional cases diagnosed during adulthood". Trabalho apresentado em Neuromuscular Disorders - 21st International Congress Of The World Muscle Society, Granada, 2016.
    Publicado
  39. R Samoes; J Oliveira; R Taipa; A Goncalves; M Cardoso; Coelho, Teresa; MM Pires; R.Santos; M.Santos. "Ryanodine-related myopathies: Clinical, histopathologic and genetic heterogeneity among 16 patients from a portuguese tertiary centre". Trabalho apresentado em Neuromuscular Disorders - 21st International Congress of the World Muscle Society, Granada, 2016.
    Publicado
  40. Alice Lopes; Alexandra Sousa; Isabel Fonseca; Margarida Branco; Carla Rodrigues; Paula Freitas; Coelho, Teresa. "Life paths of Familial Amiloidotic Polyneuropathy patients: A descriptive study". Trabalho apresentado em Orphanet Journal Of Rare Diaseases - 1st European Congress on Hereditary ATTR Amyloidosis, Paris, 2015.
    Publicado
  41. Alice Lopes; Alexandra Sousa; Isabel Fonseca; Margarida Branco; Carla Rodrigues; Paula Freitas; Coelho, Teresa. "Psychopathological dimensions in Familial Amyloid Polyneuropathy patients". Trabalho apresentado em Orphanet Journal Of Rare Diaseases - 1st European Congress on Hereditary ATTR Amyloidosis, Paris, 2015.
    Publicado
  42. Coelho, Teresa; Ana Martins da Silva; Cristina Alves; Marcio Cardoso; Cecilia Monteiro; Isabel Fonseca; Carla Rodrigues; Vanessa Costa. "Familial Amyloid Plyneuropathy treatment with Tafamidis – Evaluation of one- and two-Year treatment in Porto, Portugal". Trabalho apresentado em Orphanet Journal Of Rare Diaseases - 1st European Congress on Hereditary ATTR Amyloidosis, Paris, 2015.
    Publicado
  43. Natalia Ferreira; David Dias; Carmen Vilas Boas; Isabel Fonseca; Coelho, Teresa. "Specific ocular changes in TTR Met30-FAP after liver transplantation". Trabalho apresentado em Orphanet Journal Of Rare Diaseases - 1st European Congress on Hereditary ATTR Amyloidosis, Paris, 2015.
    Publicado
  44. Lemos, Carolina; Coelho, Teresa; Alves-Ferreira, Miguel; Santos, Diana; Sousa, Alda. "Unravelling the epidemiology of late-onset and asymptomatic carriers of FAP ATTR V30M in a portuguese population". Trabalho apresentado em 1st European Congress on Hereditary ATTR amyloidosis, Paris, 2015.
    Publicado
  45. Santos, Diana; Coelho, Teresa; Alves-Ferreira, Miguel; Sequeiros, Jorge; Alonso, Isabel; Grazina, Manuela; Sousa, Alda; Lemos, Carolina. "The hidden story behind gender differences in familial amyloidpolyneuropathy (FAP) ATTRV30M". Trabalho apresentado em 1st European Congress on Hereditary ATTR amyloidosis, Paris, 2015.
  46. Ines, Monica; Coelho, Teresa; Conceiçao, Isabel; Duarte-Ramos, Filipa; Mamede de Carvalho; Costa, Joao. "Epidemiology of transthyretin Familial Amyloid Polyneuropathy in Portugal". Trabalho apresentado em 1st European Congress on Hereditary ATTR amyloidosis, Paris, 2015.
    Publicado
  47. Adams, David; Buades, Juan; Suhr, Ole; Obici, Laura; Coelho, Teresa. "Preliminary assessment of neuropathy progression in patients with hereditary ATTR amyloidosis after orthotopic liver transplantation (OLT)". Trabalho apresentado em 1st European Congress on Hereditary ATTR amyloidosis, Paris, 2015.
    Publicado
  48. Coelho, Teresa; Adams, David; Amitay, Oved. "Patients with hereditary ATTR amyloidosis experience an increasing burden of illness as the disease progresses". Trabalho apresentado em 1st European Congress on Hereditary ATTR amyloidosis, Paris, 2015.
    Publicado
  49. Ferreira, Natalia; Dias, David; Coelho, Teresa. "Specific ophtalmologic changes in late onset familial amyloidpolyneuropathy (FAP) portuguese patients". Trabalho apresentado em 1st European Congress on Hereditary ATTR amyloidosis, Paris, 2015.
    Publicado
  50. Coelho, Teresa; A Martins da Silva; E Ackermann; MM Yamashita; S Hughes; B Monia. "Current status of ISIS-TTRRx phase 3 study in patients with transthyretin familial amyloid polyneuropathy (FAP)". Trabalho apresentado em European Journal Of Neurology - 1st Congress Of The European Academy Of Neurology, Berlin, 2015.
    Publicado
  51. Joana Martins; Isabel Moreira; Emilia Vieira; Rosario Santos; Coelho, Teresa. "Descrição de uma família com doença muscular com rippling e fraqueza distal com uma mutação no gene da Caveolina". Trabalho apresentado em Sinapse - Fórum De Neurologia 2015, Aveiro, 2015.
    Publicado
  52. Emilia Vieira; Marcia Oliveira; Rosario Santos; Manuela Santos; Ricardo Taipa; Manuel Melo Pires; Coelho, Teresa. "Distrofia muscular das cinturas tipo 2G". Trabalho apresentado em Sinapse - Reunião da Primavera da Sociedade Portuguesa de Estudos de Doenças Neuromusculares, Porto, 2015.
    Publicado
  53. Coelho, Teresa; Monteiro, C; Kristen, A; Benson, M; Karayal, O; Mundayat, R. "Transthyretin Amyloidosis Outcomes Survey (THAOS): Early symptom presentation in Hereditary Transthyretin Amyloidosis". Trabalho apresentado em Journal of Neuromuscular Diseases - 13th International Congress on Neuromuscular Diseases, Nice, 2014.
    Publicado
  54. Samoes R; Valdrez, K; Coelho, Teresa; Goncalves, I; Taipa, R; Melo Pires, M; Martins Silva, A. "Pesquisa de amilóide no ligamento transverso do carpo de doentes com Polineuropatia Amiloidótica Familiar (Val30Met) e Síndrome do Túnel Cárpico". Trabalho apresentado em Sinapse - Congresso de Neurologia 2014 (SPN), Lisboa, 2014.
    Publicado
  55. Joana Domingos; Isabel Moreira; Ana Martins da Silva; Cristina Alves; Carla Rodrigues; Coelho, Teresa. "Factors influencing TTR-FAP mean time for diagnosis". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy, Rio de Janeiro, 2013.
    Publicado
  56. Alves, C; Vilas-Boas, M; Valdrez, K; Martins da Silva, A; Pessegueiro, H; Daniel, J; Taipa, R; et al. "Domino Liver Transplantation (DLT) and De Novo Familial Amyloid Polyneuropathy (FAP) at Hospital de Santo António/Centro Hospitalar do Porto (CHP)". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy, Rio de Janeiro, 2013.
    Publicado
  57. Alves Ferreira, M; Coelho, Teresa; Santos, D.; Sequeiros, J; Alonso, I; Sousa, A.; Lemos, C. "What does the TTR Locus tell us about the variation in age-at-onset in Familial Amyloid Polyneuropathy?". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy,, Rio de Janeiro, 2013.
    Publicado
  58. Santos, D.; Coelho, Teresa; Alves Ferreira, M; Sequeiros, J; Alonso, I; Sousa, A.; Lemos, C. "Study of Apoe polymorphisms as possible modifiers of age-at-onset in Familial Amyloid Polyneuropathy (FAP ATTR V30M)". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy, Rio de Janeiro, 2013.
    Publicado
  59. Monteiro, C; Coelho, Teresa; Waddington Cruz, M; Kristen, A; Karayal, O; Mundayat, R; Stewart, M. "Transthyretin Amyloidosis Outcomes Survey (THAOS): Clinical Presentation of Symptoms Across The Disease Course For Major Genotype Groups". Trabalho apresentado em 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy, Rio de Janeiro, 2013.
    Publicado
  60. Alves, C; Martins Da Silva, A; Pessegueiro, H; Daniel, J; Taipa, R; Pires, MM; Guimares, A; Coelho, Teresa. "Domino liver transplantation (DLT) and De Novo Familial Amyloid Polyneuropathy (FAP): The Portuguese experience". Trabalho apresentado em Neurology - 65th Annual Meeting of American Academy of Neurology, San Diego, California, 2013.
    Publicado
  61. Plantbordeneuve V; Coelho, Teresa; Lawson V; Schumacher J; Mundayat, R; Karayal O; Rapezzi C. "Unravelling pheno-genotypic associations in Transthyretin Amyloidosis using data from THAOS - The Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em Neurology - 65th Annual Meeting of American Academy of Neurology, Baltimore, Maryland, 2013.
    Publicado
  62. Cardoso, Márcio; Coelho, Teresa; Mundayat, Rajiv. "Overview of patient demographics and clinical characteristics in Thaos - The Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em Neurology - 65th Annual Meeting of American Academy of Neurology, Baltimore, Maryland, 2013.
    Publicado
  63. Coelho, Teresa. "A novel and effective oral treatment for Familial Amyloid Neuropathies". Trabalho apresentado em European Journal of Neurology - 16th Congress of the European Federation of Neurologic Societies, Stockholm, 2012.
    Publicado
  64. Merlini, G; Coelho, Teresa; Judge, DP; Plantebordeneuve, V; Kelly, JW; Lombardo, I. "Transthyretin stabilization by Tafamidis in patients with Transthyretin Amyloidosis". Trabalho apresentado em European Journal of Neurology - 16th Congress of the European Federation of Neurologic Societies, Stockholm, 2012.
    Publicado
  65. Coelho, Teresa; Conceicao, I.; Plantebordeneuve, V.; Waddington Cruz, M.. "Description of Neuropathic Symptoms Reported by ATTR patients in THAOS - The Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em European Journal Of Neurology - 16th Congress Of The European Federation Of Neurologic Societies, Stockholm, 2012.
    Publicado
  66. Coelho, Teresa; Maurer, MS; Matthew, S; Plantbordeneuve, V; Rapezzi, C; Suhr, O. "Baseline demographics and clinical characteristics in THAOS - The Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em European Journal of Neurology - 16th Congress Of The European Federation Of Neurologic Societies, Stockholm, 2012.
    Publicado
  67. Santos, D.; Coelho, Teresa; Neto, J; Pinto Basto, J; Sequeiros, J; Alonso, I; Lemos, C; Sousa, A.. "APCS and RBP4 Will Act As Modifiers Of Age-At-Onset In Familial Amyloid Polyneuropathy (FAP ATTRV30M)?". Trabalho apresentado em European Journal of Epidemiology, Porto, 2012.
  68. Lemos, C; Coelho, Teresa; Martins da Silva, A; Sequeiros, J; Mendonça, D; Sousa, A.. "Anticipation Of Age-At-Onset In A Group Of Portuguese Familial Amyloid Polyneuropathy (FAP ATTRV30M) Kindreds". Trabalho apresentado em European Journal of Epidemiology - European Congress of Epidemiology 2012, Porto, 2012.
    Publicado
  69. Santos, D; Coelho, Teresa; Neto, JL; Pintobasto, J; Sequeiros, J; Alonso, I; Lemos, C; Sousa, A. "APCS and RBP4: Possible modifiers of age-at-onset in Familial Amyloid Polyneuropathy". Trabalho apresentado em European Journal Of Human Genetics - European Human Genetics Conference 2012, Nürnberg, 2012.
    Publicado
  70. Lemos, C; Coelho, Teresa; Santos, D; Neto, Jl; Alves Ferreira, M; Pinto Basto, J; Sequeiros, J; Alonso, I; Sousa, A. "Variability in age-at-onset of Familial Amyloid Polyneuropathy (Fap ATTRV30M): An extended haplotype effect?". Trabalho apresentado em European Journal of Human Genetics - European Human Genetics Conference 2012, Nürnberg, 2012.
    Publicado
  71. Sousa, A; Coelho, Teresa; Lemos, C; Mendonca, D. "The use of survival analysis to estimate age-at-onset of Familial Amyloid Polyneuropathy (FAPATTRV30M) highlights gender differences in early-onset (o.<40) patients but fails to detect it in late-onset (o.>50) patients". Trabalho apresentado em European Journal of Human Genetics - European Human Genetics Conference 2012, Nürnberg, 2012.
    Publicado
  72. Kaufman, H; Maurer, M; Coelho, Teresa; Plantebordeneuve, V; Rapezzi, C; Suhr, O. "Comparison of US and non-US patients with Familial Amyloid Polyneuropathy (FAP) and Familial Amyloid Cardiomyopathy (FAC) in THAOS". Trabalho apresentado em Neurology - 64th Annual Meeting of American Academy of Neurology, Louisiana, New Orleans, 2012.
    Publicado
  73. Coelho, Teresa; Maurer, M; Plantebordeneuve, V; Rapezzi, C Et Al.. "Baseline demographics in THAOS-The Transthyretin Amyloidosis Outcomes Survey". Trabalho apresentado em Neurology - 64th Annual Meeting of American Academy of Neurology, Louisiana, New Orleans, 2012.
    Publicado
  74. Waddington Cruz, M; Coelho, Teresa; Conceicao, I; Plantebordeneuve, V; Ericzon, BG; Falk, RH; Ikeda, SI; et al. "Baseline nutritional status in the Transthyretin Amyloidosis Outcome Survey (THAOS)". Trabalho apresentado em European Journal of Neurology - 15th Congress Of The European Federation Of Neurologic Societies, Budapest, 2011.
    Publicado
  75. Waddington Cruz, M; Coelho, Teresa; Conceicao, I; Plantebordeneuve, V; Ericzon, BG; Falk, RH; Ikeda, S; et al. "Demographics and neurologic function in early- and late-onset syptomatic patients in The Transthyretin Amyloidosis Outcomes Survey (THAOS)". Trabalho apresentado em Journal Of The Peripheral Nervous System - 2011 Meeting of the Peripheral Nerve Society, Maryland, Potomac, 2011.
    Publicado
  76. Vinik, EJ; Vinik, AI; Paulson, JF; Merkies, I; Coelho, Teresa; Grogan, D. "Validation of Norfolk QOL-DN as a measure of QOL in patients with Transthyretin Familial Amyloid Polyneuropathy". Trabalho apresentado em Journal Of The Peripheral Nervous System - 2011 Meeting of the Peripheral Nerve Society, Maryland, Potomac, 2011.
    Publicado
  77. Coelho, Teresa; Suhr, O; Adams, D; Lozeron, P; Hawkins, P; Mant, T; Stangou, A; et al. "Interim clinical update for ALN-TTR01, A Novel RNAi therapeutic for the treatment of Transthyretin Amyloidosis". Trabalho apresentado em Journal Of The Peripheral Nervous System - 2011 Meeting of the Peripheral Nerve Society, Maryland, Potomac, 2011.
    Publicado
  78. Conceicao, I; Coelho, Teresa; Plantebordeneuve, V; Waddington Cruz, M; Ericzon, B; Falk R; Ikeda, S; et al. "An evaluation of The Quality Of Life in symptomatic patients in The Transthyretin Amyloidosis Outcomes Survey (THAOS)". Trabalho apresentado em European Journal of Neurology - 21st Meeting of The European Neurological Society, Lisboa, 2011.
    Publicado
  79. Coelho, Teresa. "New pharmacological treatment. Familial Amyloid Polyneuropathy.". Trabalho apresentado em European Journal of Neurology - 21st Meeting of The European Neurological Society, Lisboa, 2011.
    Publicado
  80. Pinto-Basto, J; Sequeiros, J; Coelho, Teresa; Rocha, J; Ledo, S; Leite, A; Rolim, L; et al. "Ten year of a programme for presymptomatic testing anda prenatal diagnosis in late-onset neurological diseases in Portugal: Machado-Joseph disease, Huntington disease and familial amyloid neuropathy type I-ATTRV30M.". Trabalho apresentado em European Journal of Human Genetics - European Human Genetics Conference 2006, Amsterdam, 2006.
    Publicado
  81. Magalhães, P; Silveira, I; Coelho, Teresa; Sequeiros, J. "Frequency of 17p11.2 duplication/deletion in a group of Portuguese patients with charcot-marie-tooth type 1 (cmt1A) and hereditary neuropathy with liability to pressure palsies (HNPP).". Trabalho apresentado em European Journal of Human Genetics - European Human Genetics Conference 2006, Amsterdam, 2006.
    Publicado
  82. Cerqueira, R; Lameiras, L; Gabriel, H; Coelho, Teresa; Santos, M.; Tavares, P; Fernandes, A. "Novel mutation of the myelin P0 gene (MPZ) in a Portuguese family with cmt1B disease". Trabalho apresentado em European Journal of Human Genetics - European Human Genetics Conference 2006, Amsterdam, 2006.
    Publicado
  83. Pinto-Basto, J; Coelho, Teresa; Leal Loureiro, J; Rocha, J; Lopes, A; Sequeiros, J. "Prenatal diagnosis in late-onset neurological disorders in Portugal: experience with 83 requests, since 1996". Trabalho apresentado em European Journal of Human Genetics - European Human Genetics Conference 2006, Amsterdam, 2006.
    Publicado
  84. Sousa, A; Martins da Silva, A; Fonseca, I; Coelho, Teresa. "Familial amyloid polyneuropathy V30M in Portugal: evolutionary dynamic of a disease in expansion". Trabalho apresentado em European Journal of Human Genetics - European Human Genetics Conference 2005, Prague, 2005.
    Publicado
Tese / Dissertação
  1. Coelho, Teresa. "Disease modifying therapies for attr amyloidoses: clinical development of new drugs and impacto on the natural history of the disease". Doutoramento, 2019.
Atividades

Apresentação oral de trabalho

Título da apresentação Nome do evento
Anfitrião (Local do evento)
2020/11 Disease modifying therapies for Hereditary ATTR amyloidosis with polyneuropathy Formação Amiloidose hATTR
Sociedade Portuguesa de Medicina Interna (Portugal)
2018/10 Presente y Futuro del Tratamento de la Amiloidosis Hereditaria por Transtirretina II Jornadas Amiloidosis Hereditaria por Transtirretina
Asociación EspañolaEnfermedad de Andrade (Palma de Maiorca, Espanha)
2018/07 ANS and Amyloid European Federation Of Autonomic Societies Annual Meeting 2018
European Federation Of Autonomic Societies (Vienna, Áustria)
2018/07 The novel scenario of ATTR Amyloidosis treatment 15th International Congress on Neuromuscular Disorders
World Federation of Neurology, Applied Research Group on Neuromuscular Disorders (Vienna, Áustria)
2018/07 Identifying the transition from TTR carrier to TTR neuropathy patient 2018 Peripheral Nerve Society Annual Meeting
Peripheral Nerve Society (Baltimore, Maryland , Estados Unidos)
2018/07 Development and validation of The Transthyretin Familial Amyloid Polyneuropapathy Score (TTR-FAP Score) 2018 Peripheral Nerve Society Annual Meeting
Peripheral Nerve Society (Baltimore, Maryland, Estados Unidos)
2018/06 Validity and reliability of The Transthyretin Amyloidosis Europathy Score (TTR ANS), a new outcome measure designed specifically for Familial Amyloidpolyneuropathy (TTR-FAP) 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Inotersen improved Norfolk Quality of Life-Diabetic Neuropathy (NORFOLKQOLDN) measures in patients with Hereditary Transthyretin (HATTR) Amyloidosis treated in the Phase 3 Study Neuro-TTR 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Impact of Patisiran on Norfolk Quality Of Life Questionnaire Diabetic Neuropathy (QOL-DN) in patients with Hereditary Transthyretin-Mediated Amyloidosis: Results from the Phase 3 Apollo Study 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Impact of central nervous system and ocular phenotypes in ATTR V30M patients 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Impact of Patisiran, an investigational RNAi therapeutic, on nutritional status in patients with Hereditary Transthyretinmediated Amyloidosis 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Age-dependent cognitive dysfunction In untreated and liver transplanted ATTR V30M patients 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Outcomes of patients with Hereditary Transthyretin-Mediated Amyloidosis with early onset V30M versus all other mutations in Apollo, A Phase 3 Study of Patisiran 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Baseline characteristics of patients with Hereditary Transthyretin (HATTR) Amyloidosis with Polyneuropathy enrolled in the Phase 3 Study Neuro-TTR demonstrate significant disease burden 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Long-term efficacy and safety of Inotersen in patients with Hereditarytransthyretin (HATTR) Amyloidosis treated in the Open Label extension of the Phase 3study Neuro-TTR 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Impact of prior TTR stabilizer use in patients with Hereditary Transthyretin mediated Amyloidosis in the Apollo Phase 3 Study of Patisiran 4th Congress of the European Academy of Neurology
European Academy of Neurology (Lisboa, Portugal)
2018/06 Novos Fármacos 4º Congresso Internacional e XI Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose (Portugal)
2018/05 Impact of Hereditary Transthyretin-Mediated Amyloidosis on use of healthcare services: An analysis of the Apollo Study 9th European Conference on Rare Diseases & Orphan Products
European Organisation for Rare Diseases (EURORDIS) (Vienna, Áustria)
2018/05 Impact of Patisiran on Norfolk Quality of Life Questionnaire Diabetic Nneuropathy (QOL-DN) in patients with Hereditary Transthyretin-Mediated Amyloidosis: Results from the cardiac subpopulation in the Phase 3 Apollo Study European Society Of Cardiology – Heart Failure 2018
European Society Of Cardiology (Viena, Áustria)
2018/04 Evaluation of quality of life and disability in patients with Hereditary Transthyretin-Mediated (HATTR) Amyloidosis with Polyneuropathy following treatment with Patisiran, an investigational RNAi therapeutic: results from the Phase3 Apollo Study 70th American Academy of Neurology Annual Meeting
American Academy of Neurology (Los Angeles, California, Estados Unidos)
2018/04 Safety and efficacy of Inotersen in patients with Hereditary Transthyretin Amyloidosis Polyneuropathy (Neuro-TTR) 70th American Academy of Neurology Annual Meeting
American Academy of Neurology (Los Angeles, California, Estados Unidos)
2018/04 Inotersen improves Norfolk Quality of Life-Diabetic Neuropathy Measures in patients with Hereditary Transthyretin Amyloidosis with Polyneuropathy in the Phase3 Study Neuro-TTR 70th American Academy of Neurology Annual Meeting
American Academy of Neurology (Los Angeles, California, Estados Unidos)
2018/03 Larger normal repeats Of ATXN2 Gene may decrease age at onset in portuguese Familial Amyloid Polyneuropathy (TTR-FAP Val30Met) patients XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japão)
2018/03 Cardiac Amyloidosis in Europe: An insight through the Transthyretin Amyloidosis Outcomes Survey XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japão)
2018/03 Variants in the Transthyretin gene region as modulators of disease expressivity XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japão)
2018/03 Patisiran, an investigational RNAi therapeutic for Hereditary Transthyretin mediated Amyloidosis: Results from the Phase 3 Apollo Study XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japão)
2018/03 The cross-talk between ocular and central nervous system phenotypes in ATTRV30M patients XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japão)
2018/03 Clinical paradigms in treatment effectiveness for Hereditary Transthyretin Amyloidosis XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japão)
2018/03 Development of response to therapy and disease specific biomarkers for the Hereditary Transthyretin Amyloidoses XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japão)
2018/01/19 How I treat ATTR amyloidosis - standards and novel therapies What´s New In Amyloidosis
University Hospital of Würzburg (Würzburg, Alemanha)
2018/01/19 Introduction to ATTR amyloidosis What´s New In Amyloidosis
University Hospital of Wuerzburg (Würzburg, Alemanha)
2017/11 Transplante hepático sequencial e Polineuropatia Amiloidótica Familiar Adquirida - Experiência do Hospital de Santo António/Centro Hospitalar do Porto Congresso de Neurologia 2017
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
2017/07 The first Transthyretin Familial Amyloid Polyneuropathy gait quantification study - preliminary results 39th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC'17)
IEEE Engineering in Medicine & Biology Society (Jeju, Coreia do Sul)
2016/11 Clinical trial for TTR amyloidosis using diflunisal XI International Symposium on Amyloidosis
International Society of Amyloidosis (Woods Hole, Massachussetts, Estados Unidos)
2015/11 TTR-FAP: liver transplant vs oral medication. How and when. 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, França)
2015/11 Psychopathological dimensions in Familial Amyloid Polyneuropathy patients 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, França)
2015/11 Familial Amyloid Polyneuropathy treatment with Tafamidis – Evaluation of one- and two-year treatment in Porto, Portugal 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, França)
2015/11 Unravelling the epidemiology of late-onset and asymptomatic carriers of FAP ATTR V30M in a portuguese population 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, França)
2015/11 The hidden story behind gender differences in Familial Amyloid Polyneuropathy (FAP) ATTRV30M 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, França)
2015/09/17 De novo vitreous opacities after pars plana vitrectomy in FAP TTR Val30Met: What to do? 15th EURETINA Congress
European Society of Retina Specialists (EURETINA) (Nice, França)
2015/02 Adult Neuromuscular Disorders: Clinical Approach XLIV Conferências de Genética Doutor Jacinto Magalhães
Centro de Genética Doutor Jacinto Magalhães / Centro Hospitalar Universitário do Porto (Porto, Portugal)
2014/06 Long-term effect of Tafamidis treatment on Transthyretin Familial Amyloid Polyneuropathy (TTR-FAP): Interim results from the Fx1A-303 study Joint Congress of European Neurology
European Neurological Society and the European Federation of Neurological Societies (Istambul, Turquia)
2014/06 Tafamidis meglumine and nerve fiber function in Portuguese patients with Transthyretin Familial Amyloid Polyneuropathy Joint Congress of European Neurology
European Neurological Society and the European Federation of Neurological Societies (Istambul, Turquia)
2014/05 Extracellular matrix remodeling genes associated with age-at-onset variability in Familial Amyloid Polyneuropathy Fórum de Neurologia
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
2014/05 Age-at-onset in Familial amyloid polyneuropathy is regulated by the non-carrier haplotype? Fórum de Neurologia
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
2014/05 Familial Amyloid Polyneuropathy treatment with Tafamidis – evaluation of one year treatment at Porto XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/05 Quantification of transthyretin kinetic stability in human plasma using subunit exchange XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/05 Neuropathy progression rate in patients with Familial Amyloid Polyneuropathy XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/05 Global gene expression profiling of sex-specific inflammatory triggers of the Transthyretin Amyloidoses XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/05 Haplotype analysis: Modulation of AO through a trans-acting mechanism in Familial Amyloid Polyneuropathy XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/05 Linking extracellular matrix remodeling genes and age-at-onset variability in Familial Amyloid Polyneuropathy XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/05 Current insights into quantifying transthyretin aggregation-associated pathology and its amelioration with Tafamidis XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/04 Survival in patients with Familial Amyloid Polyneuropathy receiving Tafamidis treatment XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/04 Further analysis of Phase II Trial of Patisiran, a novel RNAi therapeutic for the treatment of Familial Amyloid Polyneuropathy XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, Estados Unidos)
2014/01 Risque d' anticipation dans la Polyneuropathie Amyloide Familiale La Polyneuropathie Amyloide Familiale – Nouveaux Enjeux?
Centre de Référence Neuropathies amyloïdes familiales (Paris, França)
2013/12 Therapeutic developments in a neurodegenerative disease, Transthyretin Amyloidosis Instituto de Medicina Molecular Monday Lectures
Instituto de Medicina Molecular (Lisboa, Portugal)
2013/11/13 Familial Amyloid Polyneuropathy TTRMet30 in Portugal: An overview 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Rio de Janeiro, Brasil)
2013/11 Summary data for Tafamidis treatment 9th International Symposium on Familial Amyloidotic polyneuropathy and XIII International Symposium on Liver Transplantation in Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Rio de Janeiro, Brasil)
2013/10 Polineuropatia Amiloidótica Familiar - Novas Terapêuticas
Centro de Genética Preditiva e Preventiva do Instituto de Biologia Molecular e Celular (Porto, Portugal)
2013/10 Doença dos Pézinhos - benefícios de um diagnóstico precoce Update em Medicina
(Póvoa De Varzim, Portugal)
2013/09 Amyloid Neuropathies XXI World Congress of Neurology
World Federation of Neurology (Vienna, Áustria)
2013/05 Variation in age-at-onset in familial amyloid polyneuropathy: an haplotype study within the TTR locus Fórum de Neurologia
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
2013/05 A candidate-gene approach to identify modifiers of age-at-onset In Familial Amyloid Polyneuropathy: the role of APCS and RBP4 genes Fórum de Neurologia
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
2013/04 Polineuropatia Amiloidótica Familiar Update em Medicina
(Albufeira, Portugal)
2013/03 Domino liver transplantation (DLT) and de novo Familial Amyloid Polyneuropathy (FAP): The portuguese experience 65th American Academy of Neurology Annual Meeting
American Academy of Neurology (San Diego, California, Estados Unidos)
2013/03 Long-Term use of Tafamidis in Transthyretin Familial Amyloid Polyneuropathy: A single center Experience 65th American Academy of Neurology Annual Meeting
American Academy of Neurology (San Diego, California, Estados Unidos)
2012/11 Novas Perspectivas de Tratamento da PAF Congresso de Neurologia 2012
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
2012/09 New approaches to the management of TTR-FAP 16th Congress of the European Federation of Neurologic Societies
European Federation of Neurologic Societies (EFNS) (Stockholm, Suécia)
2012/09 Tafamidis: A novel and effective oral treatment for Familial Amyloid Polyneuropathy 14th Congress of the European Federation of Neurologic Societies 2012
European Federation of Neurologic Societies (EFNS) (Stockholm, Suécia)
2012/05 New Approaches to the management of TTR-FAP XIII International Symposium on Amyloidosis
International Symposium on Amyloidosis (Groningen, Países Baixos)
2012/05 Familial dynamics, attachment and psychopathology in FAP patients XIII International Symposium on Amyloidosis
International Society of Amyloidosis (Groningen, Países Baixos)
2012/05 Final phase I safety, pharmacokinetic and pharmacodynamic results of ALN-TTR01, a novel RNAi therapeutic for the treatment of Transthyretin Amyloidosis XIII International Symposium on Amyloidosis
International Society of Amyloidosis (Groningen, Países Baixos)
2012/05 Novas Perspectivas de Tratamento 2.º Congresso Internacional e IX Encontro Internacional de Paramiloidose para Técnicos de Saúde
(Vila do Conde, Portugal)
2012/05 Manifestações no Sistema Nervoso Central 2.º Congresso Internacional e IX Encontro Internacional de Paramiloidose para Técnicos de Saúde
2012/05 Factores que influenciam a idade de início 2.º Congresso Internacional e IX Encontro Internacional de Paramiloidose para Técnicos de Saúde
(Vila do Conde, Portugal)
2012/04 Comparison of US and non-US Patients with Familial Amyloid Polyneuropathy (FAP) and Familial Amyloid Cardiomyopathy (FAC) in THAOS – the Transthyretin Amyloidosis Outcomes Survey 64th American Academy of Neurology Annual Meeting
American Academy of Neurology (New Orleans, Louisiana, Estados Unidos)
2011/11 Sensitivity of salivary gland biopsy in the diagnosis of early symptomatic familial amyloid polyneuropathy (ATTR Val30Met 8th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Kumamoto, Japão)
2011/11 A genetic epidemiology study of FAP (ATTRV30M) reveals important differences in age-at-onset between the two eldest Portuguese clusters, Póvoa de Varzim/Vila do Conde and Covilhã 8th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Kumamoto, Japão)
2011/11 "Amyloid Detection In Biopsy And Attr Onset In Patients From THAOS (Transthyretin Amyloidosis Outcomes Survey)” Amyloid Detection In Biopsy And Attr Onset In Patients From Thaos (Transthyretin Amyloidosis Outcomes Survey)”
8th International Symposium on Familial Amyloidotic Polyneuropathy International Society of Amyloidosis (Kumamoto, Japão)
2011/11 "Symptoms Of Onset In Patients From THAOS (Transthyretin Amyloidosis Outcomes Survey)" 8th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Kumamoto, Japão)
2011/11 "Cross-Sectional Evaluation Of Bmi And Mbmi In THAOS (Transthyretin Amyloidosis Outcomes Survey)" 8th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis
2011/09 Sensitivity of salivary gland biopsy in the diagnosis of early symptomatic Familial Amyloid Polyneuropathy 15th Congress of the European Federation of Neurological Societies
European Federation of Neurological Societies (Budapest, Hungria)
2011/06 Early-treatment effects of Tafamidis in Transthyretin Type Familial Amyloid Polyneuropathy Biennial Meeting of the Peripheral Nerve Society
Peripheral Nerve Society (Potomac, Maryland, Estados Unidos)
2011/06 Interim clinical update for ALN-TTR01, a novel RNAi therapeutic for the treatment of Transthyretin Amyloidosis Biennial Meeting of the Peripheral Nerve Society
Peripheral Nerve Society (Potomac, Maryland, Estados Unidos)
2011/05 An evaluation of the quality of life in symptomatic patients in the Transthyretin Amyloidosis Outcomes Survey (THAOS) 21st Meeting of the European Neurological Society
European Neurological Society (Lisboa, Portugal)
2011/04 Il Trattamento delle amiloidosi Transtiretina correlate Riunione dell Associazione Italiana per lo Studio del Sistema Nervoso Periferico
Associazione Italiana per lo Studio del Sistema Nervoso Periferico (Bologna, Itália)
2011/04 The long-term effects of Tafamidis for the treatment of Transthyretin Type Familial Amyloid Polyneuropathy 63th American Academy of Neurology Annual Meeting
American Academy of Neurology (Honolulu, Hawaii, Estados Unidos)
2011/03 PAF II Congresso de Medicina da AEICBAS
Instituto de Ciências Biomédicas Abel Salazar (porto, Portugal)
2010/11 Familial Amyloid Polyneuropathy: New Perspectives on Disease-Modifying Treatments Plenary Session on the LXII Reunión Annual de la Sociedad Española de Neurología
Sociedad Española de Neurología (Barcelona, Espanha)
2010/11 Apresentação dos resultados positivos do ensaio-piloto com Tafamidis em doentes com Polineuropatia Amiloidótica Familiar Congresso de Neurologia 2010
Sociedade Portuguesa de Neurologia (Espinho, Portugal)
2010/09 Sustainability of response to Tafamidis, a disease-modifying therapy for transthyretin type familial amyloid polyneuropathy 14th Congress of the European Federation of Neurological Societies
European Federation of Neurological Societies (Geneve, Suiça)
2010/09 Initial findings from the Transthyretin Amyloidosis Outcomes Survey (THAOS) – a Global Web-Based Registry 14th Congress of the European Federation of Neurological Societies
European Federation of Neurological Societies (Geneve, Suiça)
2010/08 Tafamidis (Fx-1006A): a first-in-class disease-modifying therapy for Transthyretin Familial Amyloid Rio Neuro 2010
Academia Brasileira de Neurologia (Rio de Janeiro, Brasil)
2010/08 Initial findings from the Transthyretin Amyloidosis Outcomes Survey (THAOS) – a global web-based registry Rio Neuro 2010
Academia Brasileira de Neurologia (Rio de Janeiro, Brasil)
2010/04 Assessment of organ involvement and response to the therapy in familial transthyretin amyloidosis: consensus guidelines XII International Symposium on Amyloidosis
International Society of Amyloidosis (Roma, Itália)
2010/04 ATTR transplantation consensus panel 2009 XII International Symposium on Amyloidosis
International Society of Amyloidosis (Roma, Itália)
2010/04 Initial findings from the Tranthyretin Amyloidosis Outcomes Survey (THAOS) – a global, web-based registry XII International Symposium on Amyloidosis
International Society of Amyloidosis (Roma, Itália)
2010/04 Tafamidis (Fx-1006A): a first-in-class disease-modifying therapy for Transthyretin Familial Amyloid XII International Symposium on Amyloidosis
International Society of Amyloidosis (Roma, Itália)
2010/04 Tafamidis (Fx-1006A): a first-in-class disease-modifying therapy for Transthyretin Familial Amyloid 62nd American Academy of Neurology Annual Meeting
American Academy of Neurology (Toronto, Ontario, Canadá)
2009/06 L' espoir des medicaments des NAF: le premier essai multicentrique 1ère Journée du Centre de Référence Neuropathies Amyloïdes Familiales et autres Neuropathies Periphériques Rares
Centre de Référence Neuropathies Amyloïdes Familiales et autres Neuropathies Periphériques Rares (Villejuif, França)
2009/06 THAOS – um registo internacional de amiloidoses TTR 1.º Congresso Internacional e VII Encontro Nacional de Paramiloidose para Técnicos de Saúde
(Barcelos, Portugal)
2009/06 Os Ensaios Fx005 e Fx006 1.º Congresso Internacional e VII Encontro Nacional de Paramiloidose para Técnicos de Saúde
(Barcelos, Portugal)
2009/06 A Importância do Seguimento dos Portadores Assintomáticos 1.º Congresso Internacional e VII Encontro Nacional de Paramiloidose para Técnicos de Saúde
(Barcelos, Portugal)
2009/06 Seguimento dos Receptores de Transplante Sequencial 1.º Congresso Internacional e VII Encontro Nacional de Paramiloidose para Técnicos de Saúde
(Barcelos, Portugal)
2009/06 Hospital de Santo António – 70 anos de observação 1.º Congresso Internacional e VII Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose (Barcelos, Portugal)
2009/04 Polineuropatia Amiloidótica Familiar II Congresso Recursos de Saúde em Catástrofes e Emergências
2009/04 Polineuropatias Motoras Hereditárias Reunião de Primavera 2009
Sociedade Portuguesa de Estudosde Doenças Neuromusculares (Sesimbra, Portugal)
2008/11 Polineuropatia Amiloidótica Familiar: alguns aspectos da variabilidade fenotípica Congresso de Neurologia 2008
Sociedade Portuguesa de Neurologia (Porto, Portugal)
2008/09 Rationale, design and status of the efficacy and safety trial of Fx1006A in TTR Amyloid Polyneuropathy 7th International Symposium on Familial Amyloid Polyneuropathy and 1st International Workshop on Hereditary Amyloidosis
International Society of Amyloidosis (London, Reino Unido)
2008/08 Familial Amyloid Polyneuropathy: An extraordinary model of peripheral autonomic failure 12th Congress of the European Federation of Neurological Societies
European Federation of Neurological Societies (Madrid, Espanha)
2008/04 Risk Factors in FAP transplantation 4th European Liver and Intestine Transplant Association Winter Meeting
European Liver and Intestine Transplant Association (Cortina d’Ampezzo, Itália)
2006/10 Distrofias miotónicas III Congresso Nacional de Doenças Neuromusculares
Sociedade Portuguesa de Estudosde Doenças Neuromusculares (Almansor, Portugal)
2006/05 Familial Amyloid Polyneuropathy: An extraodinary model of peripheral autonomic failure 8th European Federation of Autonomic Societies Meeting
European Federation of Autonomic Societies (Lisboa, Portugal)
2006/05 Neurovascular coupling in autonomic failure: a functional transcranial Doppler study European Federation Of Autonomic Societies Annual Meeting 2006
European Federation Of Autonomic Societies (Lisboa, Portugal)
2006/05 Ten years of a programme for presymptomatic testing and prenatal diagnosis in late-onset neurological diseases in Portugal: Machado-Joseph disease, Huntington disease and Familial Amyloid Neuropathy Type I-ATTRV30M European Human Genetics Conference 2006
European Society of Human Genetics (Amsterdam, Países Baixos)
2006/05 Avanços no Conhecimento da Polineuropatia Amiloidótica Familiar – Perspectivas de Ensaios Terapêuticos VII Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose (Covilhã, Portugal)
2006/05 Problemas dos doentes em fases inicias da doença – problemas sensitivos e perturbações gastrointestinais VII Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose (Covilhã, Portugal)
2005/11 Neuropatia periférica como apresentação de amiloidose primária Congresso de Neurologia 2005
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
2005/10 A História Natural da Paramiloidose Reunião 10 Anos – 500 Transplantes no Porto, 3.ª Reunião Paul MacMaster’s Fellows e 1.º Encontro do Capítulo Nacional do IHPBA
Centro Hospitalat Universitário do Porto (Porto, Portugal)
2005/06 Neurovascular coupling in autonomic failure: a functional transcranial Doppler study 15th Meeting of the European Neurological Society
European Neurological Society (Vienna, Áustria)
2005/05 Problemas Clínicos – Diagnóstico Precoce I Encontro da Associação Portuguesa de Paramiloidose do Cartaxo
Associação Portuguesa de Paramiloidose (Cartaxo, Portugal)
2005 Ensaios Clínicos – A Perspectiva do Clínico I Encontro da Associação Portuguesa de Paramiloidose do Cartaxo
Associação Portuguesa de Paramiloidose (Cartaxo, Portugal)
2004/11 Contribuição da avaliação neurofisiológica das pequenas fibras nervosas para a definição do início da Polineuropatia Amiloidótica Familiar Congresso de Neurologia 2004
Sociedade Portuguesa de Neurologia (Espinho, Portugal)
2004/11 Perda de variabilidade na frequência cardíaca e pressão arterial na Polineuropatia Amiloidótica – padrão craniano achatado ou invertido Congresso de Neurologia 2004
Sociedade Portuguesa de Neurologia (Espinho, Portugal)
2004/09 Genetic epidemiology of Familial Amyloid Polyneuropathy TTRMet30 in Portugal 8th Congress of the European Federation of Neurological Societies
European Federation of Neurological Societies (Paris, França)
2003/11 A Neuropatia Paramiloidótica I Jornadas de Fisiopatologia Humana
Escola Superior de Saúde do Vale do Ave (Vila Nova de Famalicão, Portugal)
2003/11 A falência autonómica afecta o acoplamento neurovascular cerebral: estudo com Doppler transcraniano funcional Congresso de Neurologia 200
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
2003/06 Diagnóstico diferencial de Distrofia das Cinturas – metodologia e revisão de grupo de doentes Fórum de Neurologia 2003
Sociedade Portuguesa de Neurologia (Luso, Portugal)
2003/05 Autonomic failure affects the Neurovascular Coupling: a FTCD study 8th Meeting of the European Society of Neurosonology and Cerebral Hemodynamics
European Society of Neurosonology and Cerebral Hemodynamics (Alicante, Espanha)
2003/03 Actualizações em Doenças Neuromusculares – Polineuropatia Amiloidótica Familiar I Congresso Nacional de Doenças Neuromusculares
Sociedade Portuguesa de Estudosde Doenças Neuromusculares (Lagoa, Portugal)
2002/09 A História Natural da Polineuropatia Amiloidótica Familiar e o Transplante Hepático XX Brazilian Congress of Neurology
Academia Brasileira de Neurologia (Florianópolis, Brasil)
2001/11 Tremor em Ortostatismo – Manifestação de um Síndrome de Sneddon Congresso de Neurologia 2001
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
2001/11 Sobrevida dos doentes com Polineuropatia Amiloidótica Familiar submetidos a transplante hepático: comparação com grupo de controle de doentes não-transplantados Congresso de Neurologia 2001
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
2001/10 A disautonomia na Polineuropatia Amiloidótica Familiar I Congresso Nacional de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Estoril, Portugal)
2001/10 Transplante hepático na Polineuropatia Amiloidótica Familiar: a experiência do Hospital de Santo António I Congresso Nacional de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Estoril, Portugal)
2001/06 Early Diagnosis of Familial Amyloid Polyneuropathy: Results of a Prospective Neurophysiological Study in Asymptomatic Carriers Seminários do IBMC
Instituto de Biologia Molecular e Celular (Porto, Portugal)
2001/03 Diagnósticos diferenciais com CMT – um caso clínico Reunião de Inverno do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Luso, Portugal)
2001/03 Uma família com três gerações de Charcot-Marie-Tooth tipo 2 Reunião de Inverno do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Luso, Portugal)
2001/03 Neuropatias Hereditárias Desmielinizantes: contributo da genética para a sua individualização Reunião de Inverno do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Luso, Portugal)
2000/10 The relative importance of patients whose parents were both unaffected in the epidemiology of Familial Amyloid Polyneuropathy I Congresso Nacional de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Estoril, Portugal)
2000/10 Clinical, neurophysiological and radiological studies of ten patients with Benign Focal Amyotrophy I Congresso Nacional de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Estoril, Portugal)
2000/10 Muscle biopsies of patients with Facioscapulohumeral Dystrophy I Congresso Nacional de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Estoril, Portugal)
2000/10 Facioscapulohumeral Muscular Dystrophy (FSHD) in Northern Portugal: a Report of 11 Families with Molecular Diagnosis I Congresso Nacional de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Estoril, Portugal)
2000/10 Clinical and Genetic Study of Myotonic Dystrophy in the North of Portugal I Congresso Nacional de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares (Estoril, Portugal)
2000/06 Utilidade do estudo neurofisiológico das pequenas fibras nervosas para o diagnóstico precoce do início da Polineuropatia Amiloidótica Familiar V Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose (Vila do Conde, Portugal)
1999/09 Familial Amyloid Polyneuropathy onset may be confirmed early by evaluation of small nerve fiber function XI International Congress of EMG and Clinical Neurophysiology
International Federation of Clinical Neurophysiology (Prague, República Checa)
1999/06 Recovery of peripheral neuropathy in FAP patients after liver transplantation: results from serial neurophysiological evaluation 4th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Umea, Suécia)
1999/06 Changes in paradigm of portuguese FAP patients: in the last 12 years, onset became later and the new families come from distinct areas 4th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Umea, Suécia)
1999/06 Genetic Epidemiology of Familial Amyloid Polyneuropathy in Majorca (Spain) 4th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Umea, Suécia)
1998/11 Dificuldades de Diagnóstico da Distrofia Muscular das Cinturas – Análise da Casuística das Consultas de Doenças Neuromusculares dos Hospitais Maria Pia e Santo António, Porto, num Período de Cinco Anos (1994-1998) Encontro do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares da da Sociedade Portuguesa de Neurologia (Luso, Portugal)
1998/11 Sarcoglicanopatias – Oito Casos Diagnosticados nas Consultas de Doenças Neuromusculares dos Hospitais Maria Pia e Santo António, Porto Encontro do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares da da Sociedade Portuguesa de Neurologia (Luso, Portugal)
1998/11 Apresentação dos primeiros casos de Distrofia das Cinturas por défice de Calpaína diagnosticadas em Portugal Encontro do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares da da Sociedade Portuguesa de Neurologia (Luso, Portugal)
1998/11 A Propósito da Experiência de Psiquiatria de Ligação com os Doentes PAF: o Ponto de Vista de uma Neurologista Ciclo de Conferências da Sociedade Portuguesa de Psicossomática 98/99
Sociedade Portuguesa de Psicossomática (Porto, Portugal)
1998/08 Anticipation of age-at-onset in portuguese patients with Familial Amyloid Polyneuropathy – Type I (FAP-Met30) VIII International Symposium on Amyloidosis and Other Transthyretin-related Disorders
International Society of Amyloidosis (Rochester, New York, Estados Unidos)
1998/05 Neuropatias Desmielinizantes: Aspectos Clínicos Encontro do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares da da Sociedade Portuguesa de Neurologia (São Pedro de Moel, Portugal)
1998/04 Polineuropatia Amiloidótica Familiar: Avaliação do Tratamento com Transplante Hepático e Imunodepuração Satellite course of the Portuguese Neurological Society Meeting: Introduction to Neurogenetics and Recent Advances
Sociedade Portuguesa de Neurologia (Aveiro, Portugal)
1997/11 O doente diabético: complicações neurológicas I Jornadas Multidisciplinares
(Espinho, Portugal)
1997/11 Polineuropatia Amiloidótica Familiar (PAF): Epidemiologia da Doença Renal em Póvoa do Varzim e Vila do Conde Jornadas de Paramiloidose 97
(Porto, Portugal)
1997/10 Estudo Genético de 18 Famílias com Distrofia Miotónica Diagnosticadas no Norte de Portugal I Reunião Científica da Sociedade Portuguesa de Genética Humana
Sociedade Portuguesa de Genética Humana (Porto, Portugal)
1997/10 Análise do Registo de Novas Famílias com Polineuropatia Amiloidótica Familiar na Última Década I Reunião Científica da Sociedade Portuguesa de Genética Humana
Sociedade Portuguesa de Genética Humana (Porto, Portugal)
1997/08 Electromyographic Evaluation of the Results of Liver Transplantation in Sixteen Patients with Familial Amyloid Polyneuropathy 14th International Congress of EEG and Clinical Neurophysiology
(Firenze, Itália)
1997/05 O Diagnóstico da Polineuropatia Amiloidótica Familiar: Questões Levantadas pela Heterogeneidade Genética e Clínica Reunião da Sociedade Portuguesa de Neurologia 1997
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
1997 O Diagnóstico da Polineuropatia Amiloidótica Familiar: Questões Levantadas pela Heterogeneidade Genética e pela Variabilidade Fenotípica Jornadas de Paramiloidose 97
(Porto, Portugal)
1996/11 Heterogeneidade Genética na Polineuropatia Amiloidótica Familiar – Implicações Diagnósticas Encontro do Grupo de Estudos de Doenças Neuromusculares
Grupo de Estudos de Doenças Neuromusculares da da Sociedade Portuguesa de Neurologia (Évora, Portugal)
1996/10 Familial Amyloid Neuropathy (FAP – type I) in Portugal: a more variable phenotype than the one first described Joint Meeting of Austrian and Portuguese Neurological Societies
Sociedade Portuguesa de Neurologia (Porto, Portugal)
1996/05 A Investigação Clínica em Hospital Central II Encontro de Saúde de Vila Real e III Jornadas do Interno do Hospital de São Pedro
(Vila Real, Portugal)
1996/05 Clinical, pathologic, biochemical and genetic studies of twenty patients with Mitochondrial Diseases Joint Meeting of Austrian and Portuguese Neurological Societies
Sociedade Portuguesa de Neurologia (Porto, Portugal)
1996/02 A Experiência da Consulta de Doenças Neuromusculares do Hospital Geral de Santo António I Jornadas de Doenças Neuromusculares
Associação Portuguesa de Doenças Neuromusculares (Porto, Portugal)
1996/01 A Experiência do Aconselhamento Genético na Polineuropatia Amiloidótica Familiar Workshop sobre Programa de Teste Preditivo e Aconselhamento Genético da Doença de Machado-Joseph
(Porto, Portugal)
1995/11 Estudo Neurofisiológico de Sete Famílias com HMSN tipo I Congresso de Neurologia 1995
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
1995/11 Apresentação Benigna em Casos de Polineuropatia Amiloidótica Familiar com Duas Mutações da Transtirretina Congresso de Neurologia 1995
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
1995/10 Variability of clinical expression in Familial Amyloid Polyneuropathy 3rd International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Lisboa, Portugal)
1995/10 Neurophysiological study of seven families with HMSN type I Spanish Neurophisiology Society Congress
Spanish Neurophisiology Society (Burgos, Espanha)
1995/10 Epidemiology and Genetic Analysis in Patients with Familial Amyloid Polyneuropathy (FAP) Type I and End-stage Renal Disease: Can we Predict Kidney Involvement? 3rd International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Lisboa, Portugal)
1995/06 Amyloid Neuropathies 5th Meeting of the European Neurological Society - Amyloid and the Nervous System Symposium
European Neurological Society (Munich, Alemanha)
1995/06 Benign Forms of Familial Amyloidotic Polyneuropathy in Compound Heterozygous Carriers of Transthyretin Met30 and Met119 5th Meeting of the European Neurological Society
European Neurological Society (Munich, Alemanha)
1995/06 End-stage Renal Disease in Familial Amyloid Polyneuropathy Type-I XXXII Congress of the European Nephrology Association
European Nephrology Association (Athens, Grécia)
1995/05 Familial Amyloid Polyneuropathy: Genetic Heterogeneity and Perspectives for Treatment Seminari di Neurologia
Istituto di Clinica Neurologica da Università di Milano (Milano, Itália)
1995/05 Critérios de Diagnóstico na Polineuropatia Amiloidótica Familia Fórum de Neurologia
Sociedade Portuguesa de Neurologia (Sintra, Portugal)
1995 Clinical Course and Outcome in Patients with Familial Amyloid Polyneuropathy (FAP) TTRMet30 on Regular Dialysis 3rd International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Lisboa, Portugal)
1995 Valor Preditivo da Biópsia no Diagnóstico da Polineuropatia Amiloidótica Familiar Congresso de Neurologia 1995
Sociedade Portuguesa de Neurologia (Sintra, Portugal)
1994/11 Motivações e Impacto do Diagnóstico Pré-sintomático na Polineuropatia Amiloidótica Familiar – 10 anos de Experiência Congresso de Neurologia 1994
Sociedade Portuguesa de Neurologia (Porto, Portugal)
1994/03 Viver com a Polineuropatia Amiloidótica Familiar XI Encontro Nacional de Clínica Geral
Associação Portuguesa de Medicina Geral Familiar (Póvoa de Varzim, Portugal)
1993/09 Questions Related to Patient Selection for Liver Transplantation in FAP 1st International Workshop on Liver Transplantation in Familial Amyloidotic Polyneuropathy
Huddinge University Hospital, Karolinska Institute (Stockholm, Suécia)
1993/01 Familial Amyloid Polyneuropapathy Public Health Course
Escola Superior de Saúde Pública (Lisboa, Portugal)
1992/10 Management do Doente com Paramiloidose 4.º Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose (Braga, Portugal)
1992/10 Mutações da TTR e Síndromes Clínicos Associados 4.º Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose
1992/09 Pathophysiology of Portuguese Familial Amyloidotic Polyneuropathy Satellite Symposium of the 6th European Congress of Clinical Neurophysiology
International Federation of Clinical Neurophysiology (Lisboa, Portugal)
1992/06 A Strikingly Benign Evolution of FAP in an Individual Found to be a Compound Heterozygote for Two TTR mutations: TTR Met30 and TTR Met119 2nd International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Skelleftea, Suécia)
1992/06 A Review of 107 Cases in Portuguese FAP Population in Whom Both Parents Were Disease-free 2nd International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Skelleftea, Suécia)
1992/06 A Compound Heterozygotic Individual for two Tranthyretin variants presenting Thyroxine Binding Capacity 2nd International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Skelleftea, Suécia)
1992/04 A Investigação Clínica da Polineuropatia Amiloidótica Familiar IBMC Draft Symposium
Centro de Citologia Experimental (Porto, Portugal)
1992/03 Doenças Étnicas Portuguesas – a Polineuropatia Amiloidótica Familiar X Temas de Medicina do Hospital Geral de Santo António
Centro Hospitalar Universitário do Porto (Porto, Portugal)
1991/06 Casos Atípicos de PAF III Encontro Nacional de Paramiloidose para Técnicos de Saúde
Associação Portuguesa de Paramiloidose (Figueira da Foz, Portugal)
1991/05 O Diagnóstico dos "Casos Esporádicos" Reunião da Sociedade Portuguesa de Neurologia 1991
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
1991/04 Complicações Neurológicas do Alcoolismo ao Nível do Sistema Nervoso Periférico I Jornadas Transmontanas de Alcoologia
Administração Regional de Saúde (Bragança, Portugal)
1991/03 Alterações Mitocondriais nas Biópsias de Músculo III Encontro de Patologistas Portugueses
Sociedade Portuguesa de Patologia Clínica (Luso, Portugal)
1991/03 Neuropatias Intersticiais Hipertróficas III Encontro de Patologistas Portugueses
Sociedade Portuguesa de Patologia Clínica (Luso, Portugal)
1990/11 A Disautonomia na Polineuropatia Amiloidótica Familiar – Avaliação por Análise Espectral da Frequência Cardíaca Congresso de Neurologia 1990
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
1990/06 Bromocriptina em Monoterapia em Doentes Parkinsónicos de novo. Estudo Longitudinal de 4 Anos Reunião da Sociedade Portuguesa de Neurologia 1990
Sociedade Portuguesa de Neurologia (Porto, Portugal)
1990/06 Disecção das Artérias Carotídeas e Vertebral – a Propósito de Alguns Casos II Congresso da Sociedade Ibero-Latino-Americana de Neurorradiologia Diagnostica e Terapêutica
Sociedade Ibero-Latino-Americana de Neurorradiologia Diagnostica e Terapêutica (Cascais, Portugal)
1990/05 Análise Espectral na Polineuropatia Amiloidótica Familiar I Congresso Nacional de Medicina Interna
Sociedade Portuguesa de Medicina Interna (Coimbra, Portugal)
1989/11 Sete Anos de Colheita de Órgãos – Algumas Considerações Congresso de Neurologia 1989
Sociedade Portuguesa de Neurologia (Lisboa, Portugal)
1989/06 Re-evaluation of the monitorization in Epilepsy II Congresso da Sociedade Espanhola de Neurofisiologia
Sociedade Espanhola de Neurofisiologia (Léon, Espanha)
1989/06 Ataxia Hereditária com Apraxia Oculomotora Reunião da Sociedade Portuguesa de Neurologia 1989
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
1989/06 Bromocriptina em baixas doses na terapêutica inicial da doença de Parkinson Reunião da Sociedade Portuguesa de Neurologia 1989
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
1988/09 La Géographie de la Polyneuropathie Amyloidotique Familiale IX Journées Internationales de Pathologie Neuromusculaire
(Marseille, França)
1988/09 Tableau Clinique de la Polyneuropathie Amyloidotique Familiale IX Journées Internationales de Pathologie Neuromusculaire
(Marseille, França)
1987/12 Neurocisticercose: Análise de 168 Casos Diagnosticados por TAC Congresso de Neurologia 1987
Sociedade Portuguesa de Neurologia (Coimbra, Portugal)
1986/05 Infecção Fúngica do Sistema Nervoso Central – A Propósito de um Caso de Aplasia Medular Joint Meeting of the Portuguese and Spanish Neurological Societies
Sociedade Espanhola de Neurologia (Salamanca, Espanha)

Orientação

Título / Tema
Papel desempenhado
Curso (Tipo)
Instituição / Organização
1997 - Atual Advisor of resident physians in the interships in Neurophysiology and Neuromuscular Disorders
Orientador
Estágios de Neurofisiologia e Doenças Neuromusculares (Curso de aperfeiçoamento / especialização)
Centro Hospitalar Universitário do Porto EPE, Portugal
2012 - 2014 Co-advisor of the Masters degree thesis "Uso de diagnóstico genético pré-implantação na Polineuropatia Amiloidótica Familiar: perspectiva dos portadores" of Katia Valdrez
Coorientador
Mestrado em Saúde Pública (Mestrado)
Universidade do Porto Faculdade de Medicina, Portugal
2012 - 2013 Advisor of the Masters degree thesis "Polineuropatia Amiloidórica Familiar. Mais um passo em direcção ao futuro" of Maria Helena Miranda Rodrigues
Orientador
Mestrado Integrado em Medicina (Mestrado) (Mestrado)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
2011 - 2012 Co-advisor of the Masters degree thesis "Manifestações urológicas e urodinâmicas precoces do doente com PAF tipo 1 (ATTRV30M), neurologicamente assintomático" of Bruno Pombo Ferreira Silva
Coorientador
Mestrado Integrado em Medicina (Mestrado)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
2010 - 2011 Advisor of the Masters degree thesis "A Polineuropatia Amiloidótica Familiar (PAF) no Concelho da Covilhã. Sua Caracterização e Breve Comparação com a Doença nos Concelhos de Póvoa de Varzim/Vila do Conde" of Maria Luísa Martins de Jesus Costa.
Coorientador
Mestrado Integrado em Medicina (Mestrado)
Universidade da Beira Interior Faculdade de Ciências da Saúde, Portugal
2006 - 2007 Advisor on the project in Neurophisiology "Diagnóstico de Polineuropatia Amiloidótica Familiar (PAF). Comparação por dois estudos neurofisiológicos" de Hélder Miguel da Silva Ferreira
Orientador
Neurofisiologia (Licenciatura/Bacharelato)
Instituto Politécnico do Porto Escola Superior de Saúde, Portugal
2004 - 2005 Advisor of the thesis "A importância da função do pacemaker em doentes com Paramiloidose, sujeitos a transplante hepático" of Anabela Severina da Silva
Orientador
Cardiopneumonologia (Licenciatura/Bacharelato)
Instituto Politécnico de Saude do Norte Escola Superior de Saúde do Vale do Ave, Portugal
2001 - 2002 Advisor on the project in Neurophisiology "Comparação entre mão dominante e não-dominante em indivíduos destros e canhotos"
Orientador
Neurofisiologia (Licenciatura/Bacharelato)
Instituto Politécnico do Porto Escola Superior de Saúde, Portugal

Participação em evento

Descrição da atividade
Tipo de evento
Nome do evento
Instituição / Organização
2014/07 - Atual "TTR-FAP: the rare disease that specialists need to know about"
Simpósio
Pfizer Symposium of the 13th International Congress on Neuromuscular Diseases
2014/07 - Atual "TTR-FAP in the clinic"
Simpósio
Pfizer Symposium of the 13th International Congress on Neuromuscular Diseases
2009/01 - Atual "Da expressão dos doentes à construção de respostas"
Encontro
Mosaico Social Encontro de Boas Práticas de Intervenção Social - Câmara Municipal de Santa Maria da Feira
2016/03/04 - 2016/03/04 "Pars Plana Vitrectomy in Amyloid Vitreous Opacities in Met30 TTR Amyloidosis After Liver Transplantation" (Joao Coelho, Ana Carolina Abreu, Natalia Ferreira, Teresa Coelho)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium V (Madrid, Spain)
2016/03/04 - 2016/03/04 "Ocular manifestations in TTR Met30 Familial Amyloid Polyneuropathy after liver transplantation" (Ana Carolina Abreu, Joao Coelho, Natalia Ferreira, Teresa Coelho)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium V (Madrid, Spain)
2015/03/06 - 2015/03/06 "Vitreous opacities as first manifestation in portuguese patients with FAP Val30Met" (David Dias, Natalia Ferreira, Teresa Coelho)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium IV (Prague, Czech Republic
2014/07/10 - 2014/07/10 "TTR-FAP Avoiding the misdiagnosis of a rare Polyneuropathy" Chair of Pfizer Symposium
Mesa-redonda
13th International Congress on Neuromuscular Diseases - Applied Research Group on Neuromuscular Diseases of the World Federation of Neurology
2014/02/07 - 2014/02/07 "Current Approaches to the Management of TTR-FAP"
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium III (Póvoa do Vazim, Portugal)
2014/02/07 - 2014/02/07 "TTR-FAP: Considerations for patient management"
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium III (Póvoa do Vazim, Portugal)
2014/02/07 - 2014/02/07 "Monitoring and assessment of patients treated with Tafamidis" (Coelho T, Conceição I, Planté-Bordeneuve V)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium III (Póvoa do Vazim, Portugal)
2013/05/23 - 2013/05/23 "Clinical experience with FAP patients"
Simpósio
19º Congresso Nacional de Medicina Interna - Simpósio Pfizer Hope
2013/04/13 - 2013/04/13 "A peculiar form of peripheric neuropaty"
Simpósio
19º Congresso Nacional de Medicina Interna - Simpósio Pfizer Hope
2013/02/02 - 2013/02/02 "Practical pharmacological approaches in the treatment of TTR-FAP" (Coelho T, Planté-Bordeneuve V)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium II (Barcelona, España)
2013/02/01 - 2013/02/01 "New approaches for the treatment of TTR-FAP"
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium II (Barcelona, España)
2013/02/01 - 2013/02/01 "Challenging cases in TTR-FAP diagnosis" (Moreira I, Domingues J, Martins Da Silva A, Coelho T)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium II (Barcelona, España)
2013/02/01 - 2013/02/01 "Factors influencing TTR-FAP mean time for diagnosis" (Moreira I, Domingues J, Martins da Silva A, Coelho T)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium II (Barcelona, España)
2012/10/13 - 2012/10/13 "Epidemiologia Genética da Polineuropatia Amiloidótica Familiar (PAF ATTR V30M)"
Outro
Vyndaqel Release Meeting
2012/02/03 - 2012/02/03 Transthyretin Amyloidosis Outcomes Survey (THAOS) (Coelho T, Rapezzi C, Suhr O)
Simpósio
Advances and Research in TTR Amyloidosis (ARiA) Symposium (Berlin, Germany)
2011/11/21 - 2011/11/21 "Organ specific impairment in FAP"
Simpósio
8th International Symposium on Familial Amyloidotic Polyneuropathy - International Society of Amyloidosis
2011/06/16 - 2011/06/16 "Levantamento Nacional"
Outro
2.º Dia Nacional de Luta Contra a Paramiloidose - Associação Portuguesa de Paramiloidose e Centro Hospitalar Universitário do Porto
2011/06/16 - 2011/06/16 "Tafamidis"
Outro
2.º Dia Nacional de Luta Contra a Paramiloidose - Associação Portuguesa de Paramiloidose e Centro Hospitalar Universitário do Porto
2010/06/16 - 2010/06/16 "Resultados de Ensaios Clínicos"
Outro
1.º Dia Nacional de Luta Contra a Paramiloidose - Associação Portuguesa de Paramiloidose e Centro Hospitalar Universitário do Porto
2010/04/20 - 2010/04/20 "Indications and timings of organ transplantation in ATTR Amyloidosis"
Mesa-redonda
XII International Symposium on Amyloidosis - International Society of Amyloidosis

Curso / Disciplina lecionado

Disciplina Curso (Tipo) Instituição / Organização
1996 - Atual Lecturer on the specialization course "Ciclo de Estudos Especiais de Neurofisiologia Clínica (CEENFC)" Ciclo de Estudos Especiais de Neurofisiologia Clínica (Diploma de especialização) Centro Hospitalar Universitário do Porto EPE, Portugal
2020/11/13 - 2020/11/13 Lecturer in "Disease modifying therapies for Hereditary ATTR amyloidosis with polyneuropathy" on the Formação Amiloidose hATTR of the Sociedade Portuguesa de Medicina Interna (Outros)
2013/05/15 - 2013/05/15 Lecturer in "Specific pharmacological treatments for TTR-FAP" on the European Advanced Postgraduate Course on Transthyretin-Associated Amyloidosis (Postgraduate Certificate)
2013/05/14 - 2013/05/14 Lecturer in "Genetic Epidemiology" on the European Advanced Postgraduate Course On Transthyretin-Associated Amyloidosis (Postgraduate Certificate)
2013/05/13 - 2013/05/13 Lecturer in "Transthyretin-Associated Amyloidosis: General aspects" on the European Advanced Postgraduate Course on Transthyretin-Associated Amyloidosis (Postgraduate Certificate)
2005 - 2006 Lecturer of Neurophysiology / Electromyography (Licenciatura) Instituto Politécnico do Porto Escola Superior de Saúde, Portugal
2002 - 2003 Lecturer of Neurophysiology / Electromyography (Licenciatura) Instituto Politécnico do Porto Escola Superior de Saúde, Portugal

Membro de associação

Nome da associação Tipo de participação
2020 - Atual International Society of Amyloidosis Member and Scientific Committee
2019 - Atual European Academy of Neurology Member
2015 - Atual Peripheral Nerve Society Member
2001 - Atual Sociedade Portuguesa de Estudos de Doenças Neuromusculares Founding partner and member (2001); President (2019-2022)
1997 - Atual Associação Portuguesa de EEG e Neurofisiologia Clínica Member
1996 - Atual Sociedade Portuguesa de Genética Humana Member and founding partner
1987 - Atual Sociedade Portuguesa de Neurologia Member

Membro de comissão

Descrição da atividade
Tipo de participação
Instituição / Organização
2020 - Atual Scientific Committee of the International Society of Amyloidosis (ISA)
Membro
2018 - 2018 Scientific Committee of the "II Jornadas Amiloidosis Hereditaria Por Transtirretina (AhTTR)" promoted by the Associación Española Enfermedad de Andrade
Membro
2013/03/31 - 2013/03/31 ALN-TTR02 Phase 3 Trial Design Discussion
Membro
2013 - 2013 Executive Committee of the International Registry Transthyretin-Associated Amyloidoses Outcomes Survey (THAOS): A Global, Multi-Center, Longitudinal, Observational Survey of Patients with Documented Transthyretin (TTR) Mutations or Wild-Type TTR Amyloidosis
Membro
2012/11/30 - 2012/11/30 Pfizer Global Medical Advisory Board: TTR-FAP associated liver transplantation - The management of patients in the post-transplant period. "The potential role for Tafamidis in the post-transplant environment"
Membro
2012/11/30 - 2012/11/30 Pfizer Global Medical Advisory Board: TTR-FAP associated liver transplantation - The management of patients in the post-transplant period. "Current Outcomes - The V30M/Endemic medical perspective"
Membro
2012/11/08 - 2012/11/09 TTR-FAP Expert Meeting . "Optimising the management of TTR-FAP in endemic environments."
Membro
2009 - 2012 Head of the International Scientific Board that coordinates the International Registry Transthyretin-Associated Amyloidoses Outcomes Survey (THAOS): A Global, Multi-Center, Longitudinal, Observational Survey of Patients with Documented Transthyretin (TTR) Mutations or Wild-Type TTR Amyloidosis".
Presidente / Vice-presidente
2011/05/06 - 2011/05/06 Guidelines Advisory Board for Transthyretin Amyloid Polyneuropathy treatment (TTR-FAP). Data Overview.
Membro
2011/05/06 - 2011/05/06 Guidelines Advisory Board for Transthyretin Amyloid Polyneuropathy treatment (TTR-FAP). Place of Tafamidis in the treatment of patients with TTR-FAP.
Membro
2010/05/25 - 2010/05/25 Review of Fx-005/Fx-006 (Clinical Trial) Results
Membro

Outro júri / avaliação

Descrição da atividade Instituição / Organização
1996 - Atual Judging panel for the specialization course "Ciclo de Estudos Especiais de Neurofisiologia Clínica (CEENFC)" Centro Hospitalar Universitário do Porto EPE, Portugal
2020 - 2020 President of the judging panel for the specialization course "Ciclo de Estudos Especiais de Neurofisiologia Clínica" Centro Hospitalar Universitário do Porto EPE, Portugal
2018 - 2018 President of the judging panel for the specialization course "Ciclo de Estudos Especiais de Neurofisiologia Clínica" Centro Hospitalar Universitário do Porto EPE, Portugal
Distinções

Prémio

2020 Prémio Bial de Medicina Clínica
Fundação Bial, Portugal
2019 Award Sollari Allegro for research projects - Best paper 2018
Centro Hospitalar Universitário do Porto EPE, Portugal
2018 Investigator Award of the European Academy Of Neurology
2017 Award Orlando Leitão for Best presentation
Sociedade Portuguesa de Neurologia, Portugal
2014 Award Sollari Allegro for research projects - Best paper 2013
Centro Hospitalar Universitário do Porto EPE, Portugal
2011 Investigator Award of the Federation of Neurological Societies
2007 Award of the Portuguese Society of Genetics for Clinical Research
1996 Best Presentation Award on the Joint Meeting of Austrian and Portuguese Neurological Societies