Identificação
Identificação pessoal
- Nome completo
- Teresa Coelho
- Data de nascimento
- 1956/10/08
- Género
- Female
Nomes de citação
- Coelho, Teresa
- Teresa Coelho
Identificadores de autor
- Ciência ID
- C71E-3343-F445
Telefones
- Telephone
-
- 222077500 Ext.: 1486 (Professional)
Moradas
- Centro Hospitalar do Porto - Hospital Santo António. Largo Abel Salazar, 4099-001, Porto, Porto, Portugal (Professional)
Domínios de atuação
- Medical and Health Sciences - Clinical Medicine - Clinical Neurology
- Medical and Health Sciences
- Medical and Health Sciences - Basic Medicine - Neurosciences
- Medical and Health Sciences - Basic Medicine - Human Genetics
Idiomas
Idioma | Conversação | Leitura | Escrita | Compreensão | Peer-review |
---|---|---|---|---|---|
English | Advanced (C1) | Advanced (C1) | Advanced (C1) | Advanced (C1) | Advanced (C1) |
French | Advanced (C1) | Advanced (C1) | Advanced (C1) | Advanced (C1) | Advanced (C1) |
Spanish; Castilian | Intermediate (B1) | Upper intermediate (B2) | Elementary (A2) | Upper intermediate (B2) | Elementary (A2) |
Portuguese (Idioma materno) |
Formação
Grau | Classificação | |
---|---|---|
2019/07/15
Concluded
|
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
Concluded
|
Neurophysiology Senior Graduate Degree (Outros)
Centro Hospitalar Universitário do Porto EPE, Portugal
|
|
2009/05/01
Concluded
|
Brachial Plexus Assessment. (Postgraduate Certificate)
American Academy of Neurology, United States
|
|
2009/05/01
Concluded
|
New Genetics: The Future Of Neurology. (Postgraduate Certificate)
American Academy of Neurology, United States
|
|
2009/04/27
Concluded
|
Autoimmune Antibody Testing In Neuropathy: Indications For Practicing Neurologist. (Postgraduate Certificate)
American Academy of Neurology, United States
|
|
2009/04/27
Concluded
|
Neuromuscular Therapy. (Postgraduate Certificate)
American Academy of Neurology, United States
|
|
1997
Concluded
|
Neurophysiology Graduate Degree (Outros)
Centro Hospitalar Universitário do Porto EPE, Portugal
|
|
1994
Concluded
|
Neurophysiology Training at the Department of Neurophysiology (Especialização pós-licenciatura)
Centro Hospitalar Universitário do Porto EPE, Portugal
|
|
1993/03
Concluded
|
Internship at the Autonomic Nervous System Studies Laboratory at the Department of Neurophysiology. (Postgraduate Certificate)
Hospital Universitario La Paz, Spain
|
|
1990
Concluded
|
Specialist in Neurology (Título de especialista)
Centro Hospitalar Universitário do Porto EPE, Portugal
|
|
1984
Concluded
|
Voluntary Residency in Intesive Care Unit (Outros)
Centro Hospitalar Universitário do Porto EPE, Portugal
|
|
1980
Concluded
|
Medicine (Licenciatura)
Universidade de Lisboa Faculdade de Medicina, Portugal
|
17 valores |
Percurso profissional
Others
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
Contract
Designação | Financiadores | |
---|---|---|
2016 - Atual | Natural history of transthyretin-mediated Familial Amyloidotic Polyneuropathy (TTR-FAP) and the impact of disease modifying
treatments
2016/002
Principal investigator
Centro Hospitalar Universitário do Porto EPE, Portugal
|
Ongoing
|
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
Principal investigator
|
Ongoing
|
2006 - Atual | Probing the Biochemical Mechanisms of Amyloid Disease
5 R01 DK0463365-16
Researcher
|
Ongoing
|
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
Concluded
|
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
Concluded
|
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
Concluded
|
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
Principal investigator
|
Concluded
|
Other
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
Principal investigator
|
Ongoing
|
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
Principal investigator
|
Ongoing
|
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
|
Ongoing
|
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
Principal investigator
|
Ongoing
|
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
|
Ongoing
|
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
Principal investigator
|
Ongoing
|
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
|
Ongoing
|
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
Principal investigator
|
Ongoing
|
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
|
Concluded
|
2018 - 2020 | PRX004-101: A Phase 1, Open-label, Dose Escalation Study of Intravenous PRX004 in Subjects with Amyloid Transthyretin (ATTR)
Amyloidosis
PRX004-101
Researcher
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
2009 - 2013 | Open-Label Safety and Efficacy Evaluation of Fx-1006A in Patients with Transthyretin Amyloidosis
Fx-1006A ext2
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
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
Principal investigator
|
Concluded
|
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
|
Concluded
|
Produções
Publications
Book chapter |
|
Conference abstract |
|
Conference poster |
|
Journal article |
|
Thesis / Dissertation |
|
Atividades
Oral presentation
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, Spain)
|
2018/07 | ANS and Amyloid | European Federation Of Autonomic Societies Annual Meeting 2018
European Federation Of Autonomic Societies (Vienna, Austria)
|
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, Austria)
|
2018/07 | Identifying the transition from TTR carrier to TTR neuropathy patient | 2018 Peripheral Nerve Society Annual Meeting
Peripheral Nerve Society (Baltimore, Maryland , United States)
|
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, United States)
|
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, Austria)
|
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, Austria)
|
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, United States)
|
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, United States)
|
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, United States)
|
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, Japan)
|
2018/03 | Cardiac Amyloidosis in Europe: An insight through the Transthyretin Amyloidosis Outcomes Survey | XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japan)
|
2018/03 | Variants in the Transthyretin gene region as modulators of disease expressivity | XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japan)
|
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, Japan)
|
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, Japan)
|
2018/03 | Clinical paradigms in treatment effectiveness for Hereditary Transthyretin Amyloidosis | XVIth International Symposium on Amyloidosis
International Society of Amyloidosis (Kumamoto, Japan)
|
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, Japan)
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2018/01/19 | How I treat ATTR amyloidosis - standards and novel therapies | What´s New In Amyloidosis
University Hospital of Würzburg (Würzburg, Germany)
|
2018/01/19 | Introduction to ATTR amyloidosis | What´s New In Amyloidosis
University Hospital of Wuerzburg (Würzburg, Germany)
|
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, South Korea)
|
2016/11 | Clinical trial for TTR amyloidosis using diflunisal | XI International Symposium on Amyloidosis
International Society of Amyloidosis (Woods Hole, Massachussetts, United States)
|
2015/11 | TTR-FAP: liver transplant vs oral medication. How and when. | 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, France)
|
2015/11 | Psychopathological dimensions in Familial Amyloid Polyneuropathy patients | 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, France)
|
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, France)
|
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, France)
|
2015/11 | The hidden story behind gender differences in Familial Amyloid Polyneuropathy (FAP) ATTRV30M | 1st European Congress on Hereditary ATTR Amyloidosis
(Paris, France)
|
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, France)
|
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, Turkey)
|
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, Turkey)
|
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, United States)
|
2014/05 | Quantification of transthyretin kinetic stability in human plasma using subunit exchange | XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, United States)
|
2014/05 | Neuropathy progression rate in patients with Familial Amyloid Polyneuropathy | XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, United States)
|
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, United States)
|
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, United States)
|
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, United States)
|
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, United States)
|
2014/04 | Survival in patients with Familial Amyloid Polyneuropathy receiving Tafamidis treatment | XIV International Symposium on Amyloidosis
International Society of Amyloidosis (Indianapolis, Indiana, United States)
|
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, United States)
|
2014/01 | Risque d' anticipation dans la Polyneuropathie Amyloide Familiale | La Polyneuropathie Amyloide Familiale – Nouveaux Enjeux?
Centre de Référence Neuropathies amyloïdes familiales (Paris, France)
|
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, Brazil)
|
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, Brazil)
|
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, Austria)
|
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, United States)
|
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, United States)
|
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, Sweden)
|
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, Sweden)
|
2012/05 | New Approaches to the management of TTR-FAP | XIII International Symposium on Amyloidosis
International Symposium on Amyloidosis (Groningen, Netherlands)
|
2012/05 | Familial dynamics, attachment and psychopathology in FAP patients | XIII International Symposium on Amyloidosis
International Society of Amyloidosis (Groningen, Netherlands)
|
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, Netherlands)
|
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, United States)
|
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, Japan)
|
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, Japan)
|
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, Japan)
|
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, Japan)
|
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, Hungary)
|
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, United States)
|
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, United States)
|
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, Italy)
|
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, United States)
|
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, Spain)
|
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, Switzerland)
|
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, Switzerland)
|
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, Brazil)
|
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, Brazil)
|
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, Italy)
|
2010/04 | ATTR transplantation consensus panel 2009 | XII International Symposium on Amyloidosis
International Society of Amyloidosis (Roma, Italy)
|
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, Italy)
|
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, Italy)
|
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, Canada)
|
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, France)
|
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, United Kingdom)
|
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, Spain)
|
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, Italy)
|
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, Netherlands)
|
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, Austria)
|
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, France)
|
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, Spain)
|
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, Brazil)
|
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, Czech Republic)
|
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, Sweden)
|
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, Sweden)
|
1999/06 | Genetic Epidemiology of Familial Amyloid Polyneuropathy in Majorca (Spain) | 4th International Symposium on Familial Amyloidotic Polyneuropathy
International Society of Amyloidosis (Umea, Sweden)
|
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, United States)
|
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, Italy)
|
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, Spain)
|
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, Germany)
|
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, Germany)
|
1995/06 | End-stage Renal Disease in Familial Amyloid Polyneuropathy Type-I | XXXII Congress of the European Nephrology Association
European Nephrology Association (Athens, Greece)
|
1995/05 | Familial Amyloid Polyneuropathy: Genetic Heterogeneity and Perspectives for Treatment | Seminari di Neurologia
Istituto di Clinica Neurologica da Università di Milano (Milano, Italy)
|
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, Sweden)
|
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, Sweden)
|
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, Sweden)
|
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, Sweden)
|
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, Spain)
|
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, France)
|
1988/09 | Tableau Clinique de la Polyneuropathie Amyloidotique Familiale | IX Journées Internationales de Pathologie Neuromusculaire
(Marseille, France)
|
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, Spain)
|
Supervision
Título / Tema Papel desempenhado |
Curso (Tipo) Instituição / Organização |
|
---|---|---|
1997 - Atual | Advisor of resident physians in the interships in Neurophysiology and Neuromuscular Disorders
Supervisor
|
Estágios de Neurofisiologia e Doenças Neuromusculares (Specialization course)
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
Co-supervisor
|
Mestrado em Saúde Pública (Master)
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
Supervisor
|
Mestrado Integrado em Medicina (Mestrado) (Master)
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
Co-supervisor
|
Mestrado Integrado em Medicina (Master)
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.
Co-supervisor
|
Mestrado Integrado em Medicina (Master)
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
Supervisor
|
Neurofisiologia (Degree)
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
Supervisor
|
Cardiopneumonologia (Degree)
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"
Supervisor
|
Neurofisiologia (Degree)
Instituto Politécnico do Porto Escola Superior de Saúde, Portugal
|
Event participation
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"
Symposium
|
Pfizer Symposium of the 13th International Congress on Neuromuscular Diseases |
2014/07 - Atual | "TTR-FAP in the clinic"
Symposium
|
Pfizer Symposium of the 13th International Congress on Neuromuscular Diseases |
2009/01 - Atual | "Da expressão dos doentes à construção de respostas"
Meeting
|
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)
Symposium
|
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)
Symposium
|
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)
Symposium
|
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
Round table
|
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"
Symposium
|
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"
Symposium
|
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)
Symposium
|
Advances and Research in TTR Amyloidosis (ARiA) Symposium III (Póvoa do Vazim, Portugal) |
2013/05/23 - 2013/05/23 | "Clinical experience with FAP patients"
Symposium
|
19º Congresso Nacional de Medicina Interna - Simpósio Pfizer Hope |
2013/04/13 - 2013/04/13 | "A peculiar form of peripheric neuropaty"
Symposium
|
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)
Symposium
|
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"
Symposium
|
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)
Symposium
|
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)
Symposium
|
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)"
Other
|
Vyndaqel Release Meeting |
2012/02/03 - 2012/02/03 | Transthyretin Amyloidosis Outcomes Survey (THAOS) (Coelho T, Rapezzi C, Suhr O)
Symposium
|
Advances and Research in TTR Amyloidosis (ARiA) Symposium (Berlin, Germany) |
2011/11/21 - 2011/11/21 | "Organ specific impairment in FAP"
Symposium
|
8th International Symposium on Familial Amyloidotic Polyneuropathy - International Society of Amyloidosis |
2011/06/16 - 2011/06/16 | "Levantamento Nacional"
Other
|
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"
Other
|
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"
Other
|
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"
Round table
|
XII International Symposium on Amyloidosis - International Society of Amyloidosis |
Association member
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 |
Committee member
Descrição da atividade Tipo de participação |
Instituição / Organização | |
---|---|---|
2020 - Atual | Scientific Committee of the International Society of Amyloidosis (ISA)
Member
|
|
2018 - 2018 | Scientific Committee of the "II Jornadas Amiloidosis Hereditaria Por Transtirretina (AhTTR)" promoted by the Associación
Española Enfermedad de Andrade
Member
|
|
2013/03/31 - 2013/03/31 | ALN-TTR02 Phase 3 Trial Design Discussion
Member
|
|
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
Member
|
|
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"
Member
|
|
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"
Member
|
|
2012/11/08 - 2012/11/09 | TTR-FAP Expert Meeting . "Optimising the management of TTR-FAP in endemic environments."
Member
|
|
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".
President / Vice-president
|
|
2011/05/06 - 2011/05/06 | Guidelines Advisory Board for Transthyretin Amyloid Polyneuropathy treatment (TTR-FAP). Data Overview.
Member
|
|
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.
Member
|
|
2010/05/25 - 2010/05/25 | Review of Fx-005/Fx-006 (Clinical Trial) Results
Member
|
Course / Discipline taught
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 |
Other jury / evaluation
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
Award
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 |