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Teresa Maria Pereira Padrão Temudo. Concluiu o(a) Doutoramento em n/a em 2008 pelo(a) Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar. Recebeu 5 prémio(s) e/ou homenagens. Atua na(s) área(s) de Ciências Médicas e da Saúde com ênfase em Medicina Clínica com ênfase em Neurologia Clínica, Ciências Médicas e da Saúde com ênfase em Medicina Clínica com ênfase em Neurologia Clínica e Ciências Médicas e da Saúde com ênfase em Medicina Clínica com ênfase em Neurologia Clínica.
Identification

Personal identification

Full name
Teresa Maria Pereira Padrão Temudo

Citation names

  • Temudo, Teresa

Author identifiers

Ciência ID
931B-2ADA-BA6D

Knowledge fields

  • Medical and Health Sciences - Clinical Medicine - Clinical Neurology
  • Medical and Health Sciences - Clinical Medicine - Clinical Neurology
  • Medical and Health Sciences - Clinical Medicine - Clinical Neurology

Languages

Language Speaking Reading Writing Listening Peer-review
English Advanced (C1) Advanced (C1) Advanced (C1) Advanced (C1)
French Advanced (C1) Advanced (C1) Advanced (C1) Advanced (C1)
Spanish; Castilian Intermediate (B1) Advanced (C1) Beginner (A1) Intermediate (B1)
Education
Degree Classification
2008
Concluded
Ciências Biomédicas (Doutoramento)
Major in Neurociências
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
"Clinical and Genetic Study of Rett Syndrome in Portugal" (THESIS/DISSERTATION)
Unanimidade com Distinção e Louvor
Affiliation

Teaching in Higher Education

Category
Host institution
Employer
2008 - Current Invited Associate Professor (University Teacher) Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal

Other Careers

Category
Host institution
Employer
2020 - Current Assistente graduado sénior (Médica) Centro Hospitalar Universitário do Porto EPE, Portugal
Centro Hospitalar Universitário do Porto EPE, Portugal

Others

Category
Host institution
Employer
2011/01/01 - Current Head of Paediatric Neurology Unit Centro Hospitalar Universitário do Porto EPE Centro Materno-Infantil do Norte Dr Albino Aroso, Portugal
1993/01/01 - 1995/12/31 Training of Neuropediatrics at Serviço de Neuropediatria do Hospital Maria Pia, Porto. Centro Hospitalar Universitário do Porto EPE, Portugal
1994/03/01 - 1994/07/31 Fellowship at Serviço de Neuropediatria do Hospital de San Juan de Diós, Barcelona with a grant from Fundação Calouste Gulbenkian Hospital de Sant Joan de Déu, Spain
1987/03/01 - 1992/12/31 Training of Pediatrics at Serviço de Pediatria do Hospital Geral de Santo António. Centro Hospitalar Universitário do Porto EPE, Portugal
1992/06/01 - 1992/10/31 Fellowship at Centre d'Études Prospectives de Development do Sérvice de Neonatologie du C.H.U.V., Lausanne, Switzerland Centre Hospitalier Universitaire Site de l'Hôpital de l'enfance de Lausanne, Switzerland
1991/03/01 - 1991/06/30 Fellowship at Sérvice de Neuropédiatrie da Clinique Saint-Luc em Bruxelles, Belgic. Cliniques universitaires Saint-Luc, Belgium
Projects

Contract

Designation Funders
2014 - 2015 Project Neurodegeneració amb acumulació cerebral de ferro. Evaluació clínica i caracterizació genética a través de una xarxa d’investigació multicêntrica espanyola
20143130
Researcher
2013 - 2014 Movement Disorders in Autism Spectrum Disorder
PTDC/NEU-SCC/0767/2012
Principal investigator
Concluded
2007 - 2011 Atraso Mental idiopático: avaliação de um estratégia de CGH microarrays para diagnóstico genético
PIC/IC/83026/2007
Researcher
2007 - 2011 Estudo clínico e genético do atraso mental ligado ao X em Portugal: validação de um painel de genes para diagnóstico
PIC/IC/83013/2007
Researcher
2001 - 2005 Estudo clínico, epidemiológico e genético de Síndrome de Rett em Portugal
POCTI/41416/2001
Researcher
Outputs

Publications

Journal article
  1. Martins, Joana; Darling, Alejandra; Garrido, Cristina; Espinós, Carmen; Martí, María José; Dueñas, Belen Pérez; Temudo, Teresa. "Sensory Tricks in Pantothenate Kinase-Associated Neurodegeneration: Video-Analysis of 43 Patients". Movement Disorders Clinical Practice 6 8 (2019): 704-707. http://dx.doi.org/10.1002/mdc3.12842.
    10.1002/mdc3.12842
  2. Melo, Cláudia; Ruano, Luís; Jorge, Joana; Pinto Ribeiro, Tiago; Oliveira, Guiomar; Azevedo, Luís; Temudo, Teresa. "Prevalence and determinants of motor stereotypies in autism spectrum disorder: A systematic review and meta-analysis". Autism 24 3 (2019): 569-590. http://dx.doi.org/10.1177/1362361319869118.
    10.1177/1362361319869118
  3. Lopes, Fátima; Torres, Fátima; Soares, Gabriela; Barbosa, Mafalda; Silva, João; Duque, Frederico; Rocha, Miguel; et al. "Genomic imbalances defining novel intellectual disability associated loci". Orphanet Journal of Rare Diseases 14 1 (2019): http://dx.doi.org/10.1186/s13023-019-1135-0.
    10.1186/s13023-019-1135-0
  4. Darling, Alejandra; Aguilera-Albesa, Sergio; Tello, Cristina Aisha; Serrano, Mercedes; Tomás, Miguel; Camino-León, Rafael; Fernández-Ramos, Joaquín; et al. "PLA2G6-associated neurodegeneration: New insights into brain abnormalities and disease progression". Parkinsonism & Related Disorders 61 (2019): 179-186. http://dx.doi.org/10.1016/j.parkreldis.2018.10.013.
    10.1016/j.parkreldis.2018.10.013
  5. Darling, Alejandra; Tello, Cristina; Martí, María Josep; Garrido, Cristina; Aguilera-Albesa, Sergio; Tomás Vila, Miguel; Gastón, Itziar; et al. "Clinical rating scale for pantothenate kinase-associated neurodegeneration: A pilot study". Movement Disorders 32 11 (2017): 1620-1630. http://dx.doi.org/10.1002/mds.27129.
    10.1002/mds.27129
  6. Lopes, Fátima; Barbosa, Mafalda; Ameur, Adam; Soares, Gabriela; de Sá, Joaquim; Dias, Ana Isabel; Oliveira, Guiomar; et al. "Identification of novel genetic causes of Rett syndrome-likephenotypes". Journal of Medical Genetics 53 3 (2016): 190-199. http://dx.doi.org/10.1136/jmedgenet-2015-103568.
    10.1136/jmedgenet-2015-103568
  7. Vieira, José Pedro; Lopes, Fátima; Silva-Fernandes, Anabela; Sousa, Maria Vânia; Moura, Sofia; Sousa, Susana; Costa, Bruno M.; et al. "Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene". International Journal of Developmental Neuroscience 46 C (2015): 82-87. http://dx.doi.org/10.1016/j.ijdevneu.2015.07.010.
    10.1016/j.ijdevneu.2015.07.010
  8. Patterson, Marc C; Mengel, Eugen; Vanier, Marie T; Schwierin, Barbara; Muller, Audrey; Cornelisse, Peter; Pineda, Mercè. "Stable or improved neurological manifestations during miglustat therapy in patients from the international disease registry for Niemann-Pick disease type C: an observational cohort study". Orphanet Journal of Rare Diseases 10 1 (2015): http://dx.doi.org/10.1186/s13023-015-0284-z.
    10.1186/s13023-015-0284-z
  9. Monteiro, T.; Garrido, C.; Pina, S.; Chorão, R.; Carrilho, I.; Figueiroa, S.; Santos, M.; Temudo, T.. "Esclerosis tuberosa: caracterización clínica e intento de correlación fenotipo/genotipo". Anales de Pediatría 81 5 (2014): 289-296. http://dx.doi.org/10.1016/j.anpedi.2014.03.022.
    10.1016/j.anpedi.2014.03.022
  10. Barros, Pedro; Brito, Hernâni; Ferreira, Paula Cristina; Ramalheira, João; Lopes, João; Rangel, Rui; Temudo, Teresa; Figueiroa, Sónia. "Resective surgery in the treatment of super-refractory partial status epilepticus secondary to NMDAR antibody encephalitis". European Journal of Paediatric Neurology 18 3 (2014): 449-452. http://dx.doi.org/10.1016/j.ejpn.2014.01.013.
    10.1016/j.ejpn.2014.01.013
  11. Rios, M.; Barbot, C.; Pinto, P.S.; Salício, L.; Santos, M.; Carrilho, I.; Temudo, T.. "Síndrome de Sturge-Weber: variabilidad clínica y de neuroimagen". Anales de Pediatría 77 6 (2012): 397-402. http://dx.doi.org/10.1016/j.anpedi.2012.03.004.
    10.1016/j.anpedi.2012.03.004
  12. Goldman, Sylvie; Temudo, Teresa. "Hand stereotypies distinguish Rett syndrome from autism disorder". Movement Disorders 27 8 (2012): 1060-1062. http://dx.doi.org/10.1002/mds.25057.
    10.1002/mds.25057
  13. Fasano, Alfonso; Ricciardi, Lucia; Bentivoglio, Anna Rita; Canavese, Carlotta; Zorzi, Giovanna; Petrovic, Igor; Kresojevic, Nikola; et al. "Status dystonicus: Predictors of outcome and progression patterns of underlying disease". Movement Disorders 27 6 (2012): 783-788. http://dx.doi.org/10.1002/mds.24981.
    10.1002/mds.24981
  14. Temudo, Teresa; Santos, Mónica; Ramos, Elisabete; Dias, Karin; Vieira, José Pedro; Moreira, Ana; Calado, Eulália; et al. "Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes". Brain and Development 33 1 (2011): 69-76. http://dx.doi.org/10.1016/j.braindev.2010.01.004.
    10.1016/j.braindev.2010.01.004
  15. Pineda, M.; Perez-Poyato, M.S.; O’Callaghan, M.; Vilaseca, M.A.; Pocovi, M.; Domingo, R.; Ruiz Portal, L.; et al. "Clinical experience with miglustat therapy in pediatric patients with Niemann–Pick disease type C: A case series". Molecular Genetics and Metabolism 99 4 (2010): 358-366. http://dx.doi.org/10.1016/j.ymgme.2009.11.007.
    10.1016/j.ymgme.2009.11.007
  16. Prior, C.; Nunes, A.; Rios, M.; Sequeiros, J.; Maciel, P.; Gomes, L.; Temudo, T.. "Trastornos nutricionales y gastrointestinales en el síndrome de Rett: importancia de la intervención temprana". Anales de Pediatría 72 3 (2010): 191-198. http://dx.doi.org/10.1016/j.anpedi.2009.02.007.
    10.1016/j.anpedi.2009.02.007
  17. Vieira, J.P.; Luis, C.; Monteiro, J.P.; Temudo, T.; Campos, M.M.; Quintas, S.; Nunes, S.. "Cerebral sinovenous thrombosis in children: Clinical presentation and extension, localization and recanalization of thrombosis". European Journal of Paediatric Neurology 14 1 (2010): 80-85. http://dx.doi.org/10.1016/j.ejpn.2008.12.004.
    10.1016/j.ejpn.2008.12.004
  18. Santos, Mónica; Temudo, Teresa; Kay, Teresa; Carrilho, Inês; Medeira, Ana; Cabral, Helena; Gomes, Roseli; et al. "Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients". Journal of Child Neurology 24 1 (2009): 49-55. http://dx.doi.org/10.1177/0883073808321043.
    10.1177/0883073808321043
  19. Temudo, T.; Rios, M.; Prior, C.; Carrilho, I.; Santos, M.; Maciel, P.; Sequeiros, J.; et al. "Evaluation of CSF neurotransmitters and folate in 25 patients with Rett disorder and effects of treatment". Brain and Development 31 1 (2009): 46-51. http://dx.doi.org/10.1016/j.braindev.2008.05.003.
    10.1016/j.braindev.2008.05.003
  20. Temudo, Teresa; Ramos, Elisabete; Dias, Karin; Barbot, Clara; Vieira, Jose P.; Moreira, Ana; Calado, Eulalia; et al. "Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type". Movement Disorders 23 10 (2008): 1384-1390. http://dx.doi.org/10.1002/mds.22115.
    10.1002/mds.22115
  21. Temudo, Teresa; Freitas, Paula; Sequeiros, Jorge; Maciel, Patricia; Oliveira, Guiomar. "Atypical stereotypies and vocal tics in Rett syndrome: An illustrative case". Movement Disorders 23 4 (2008): 622-624. http://dx.doi.org/10.1002/mds.21939.
    10.1002/mds.21939
  22. Santos, Mónica; Yan, Jin; Temudo, Teresa; Oliveira, Guiomar; Vieira, José Pedro; Fen, Jinong; Sommer, Steve; Maciel, Patrícia. "Analysis of Highly Conserved Regions of the 3’UTR ofMECP2Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation". Disease Markers 24 6 (2008): 319-324. http://dx.doi.org/10.1155/2008/738401.
    10.1155/2008/738401
  23. Castro, M-J; Nunes, B; De Vries, B; Lemos, C; Vanmolkot, KRJ; Van Den Heuvel, JJMW; Temudo, T; et al. "Two novel functional mutations in the Na+,K+-ATPase a2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes". Clinical Genetics 73 1 (2007): 37-43. http://dx.doi.org/10.1111/j.1399-0004.2007.00918.x.
    10.1111/j.1399-0004.2007.00918.x
  24. Ramaekers, V.; Sequeira, J.; Artuch, R.; Blau, N.; Temudo, T.; Ormazabal, A.; Pineda, M.; et al. "Folate Receptor Autoantibodies and Spinal Fluid 5-Methyltetrahydrofolate Deficiency in Rett Syndrome". Neuropediatrics 38 4 (2007): 179-183. http://dx.doi.org/10.1055/s-2007-991148.
    10.1055/s-2007-991148
  25. Marini, Carla; Mei, Davide; Temudo, Teresa; Ferrari, Anna Rita; Buti, Daniela; Dravet, Charlotte; Dias, Ana I.; et al. "Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities". Epilepsia 48 9 (2007): 1678-1685. http://dx.doi.org/10.1111/j.1528-1167.2007.01122.x.
    10.1111/j.1528-1167.2007.01122.x
  26. Temudo, T.; Oliveira, P.; Santos, M.; Dias, K.; Vieira, J.; Moreira, A.; Calado, E.; et al. "Stereotypies in Rett syndrome: Analysis of 83 patients with and without detected MECP2 mutations". Neurology 68 15 (2007): 1183-1187. http://dx.doi.org/10.1212/01.wnl.0000259086.34769.78.
    10.1212/01.wnl.0000259086.34769.78
  27. Catarina Prior, A.; Tavares, S.; Figueiroa, S.; Temudo, T.. "Tics en niños y adolescentes: análisis retrospectivo de 78 casos". Anales de Pediatría 66 2 (2007): 129-134. http://dx.doi.org/10.1157/13098929.
    10.1157/13098929
  28. Temudo, Teresa; Maciel, Patricia; Sequeiros, Jorge. "Abnormal movements in Rett syndrome are present before the regression period: A case study". Movement Disorders 22 15 (2007): 2284-2287. http://dx.doi.org/10.1002/mds.21744.
    10.1002/mds.21744
  29. Coutinho, Ana M.; Oliveira, Guiomar; Katz, Cécile; Feng, Jinong; Yan, Jin; Yang, Chunmei; Marques, Carla; et al. "MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients". American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B 4 (2007): 475-483. http://dx.doi.org/10.1002/ajmg.b.30490.
    10.1002/ajmg.b.30490
  30. Temudo, Teresa. "Rolandic epilepsy. An analysis of the clinical and electrophysiological characteristics, treatment and prognosis in 87 patients". Revista de Neurología (2005):
  31. Shi, Jinxiu; Shibayama, Akane; Liu, Qiang; Nguyen, Vu Q.; Feng, Jinong; Santos, M¿nica; Temudo, Teresa; Maciel, Patricia; Sommer, Steve S.. "Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR)". Human Mutation 25 5 (2005): 505-505. http://dx.doi.org/10.1002/humu.9338.
    10.1002/humu.9338
  32. Temudo, Teresa. "Movement disorders in Rett syndrome". Revista de Neurología (2005):
  33. Temudo, Teresa; Martins, Esmeralda; Poças, Fátima; Cruz, Romeu; Vilarinho, Laura. "Maple syrup disease presenting as paroxysmal dystonia". Annals of Neurology 56 5 (2004): 749-750. http://dx.doi.org/10.1002/ana.20288.
    10.1002/ana.20288
  34. Temudo, Teresa. "Schilder's disease: two new cases and a review of the literature". Revista de Neurología (2004):
  35. Temudo, Teresa. "Paroxysmal dyskinesias in children". Revista de Neurología (2004):
  36. Temudo, Teresa; Espinheira de Sá Maciel, Patricia. "Síndrome de Rett. Características clínicas y avances genéticos". Revista de Neurología 34 S1 (2002): 54. http://dx.doi.org/10.33588/rn.34s1.2002031.
    10.33588/rn.34s1.2002031
  37. Moreira Ramos, Sandra María; Padrao Temudo, Teresa. "Síndrome de opsoclono-mioclono: ¿hasta cuándo seguir investigando?". Revista de Neurología 35 04 (2002): 322. http://dx.doi.org/10.33588/rn.3504.2000403.
    10.33588/rn.3504.2000403
  38. Cunha, Joaquim; Madalena, Célia; Azevedo Guimarães, Paulo Fernando; Sousa, Armando; Temudo, Teresa. "Infección por Myoplasma Pneumoniae: tres casos con complicaciones neurológicas". Revista de Neurología 34 11 (2002): 1053. http://dx.doi.org/10.33588/rn.3411.2001499.
    10.33588/rn.3411.2001499
  39. Garrido, Cristina; Tuna, Assunção; Moreira Ramos, Sandra María; Temudo, Teresa. "Cefalea en racimos en una niña de 3 años". Revista de Neurología 33 08 (2001): 732. http://dx.doi.org/10.33588/rn.3308.2001051.
    10.33588/rn.3308.2001051
  40. Temudo, Teresa. "X-linked hydrocephalus (Brickers-Adams syndrome). A case report confirmed by molecular genetic studies". Revista de Neurología (2000):
  41. Temudo, Teresa. "Status epilepticus in the childhood. A review of seven years". Revista de Neurología (2000):
  42. Pineda, M; Pavia, C; Vilaseca, M A; Ferrer, I; Temudo, T; Chabas, A; Stibler, H; Jaeken, J. "Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome.". Archives of Disease in Childhood 74 3 (1996): 242-243. http://dx.doi.org/10.1136/adc.74.3.242.
    10.1136/adc.74.3.242
  43. Pineda, Merce; Campistol, Jaume; Vilaseca, M. Antonia; Briones, Paz; Ribes, Antonia; Temudo, Teresa; Pons, Marti; Cusi, Victoria; Rolland, Marie-Odile. "An atypical French form of pyruvate carboxylase deficiency". Brain and Development 17 4 (1995): 276-279. http://dx.doi.org/10.1016/0387-7604(95)00057-i.
    10.1016/0387-7604(95)00057-i
Distinctions

Other distinction

2010 3th prize Professor Doutor Amândio Tavares
2009 Prize for the best scientific publication of Centro Hospitalar do Porto
Centro Hospitalar Universitário do Porto EPE, Portugal
2008 2th prize Fundação Amélia Mello
2007 Anual prize of Liga Portuguesa Contra a Epilepsia
2005 Anual prize of Liga Portuguesa Contra a Epilepsia