???global.info.a_carregar???
Claudia Melo. Concluiu o(a) Doutoramento em Investigação Clínica e em Serviços de Saúde em 2022/11/25 pelo(a) Universidade do Porto Faculdade de Medicina. É Professor Auxiliar Convidado no(a) Universidade do Porto Faculdade de Medicina. Publicou 27 artigos em revistas especializadas. Atua na(s) área(s) de Ciências Médicas e da Saúde com ênfase em Medicina Clínica com ênfase em Pediatria.
Identificação

Identificação pessoal

Nome completo
Claudia Melo

Nomes de citação

  • Melo, Claudia

Identificadores de autor

Ciência ID
521D-0311-620E
ORCID iD
0000-0002-3215-1191

Telefones

Telemóvel
  • (351) 963172300 (Pessoal)

Domínios de atuação

  • Ciências Médicas e da Saúde - Medicina Clínica - Pediatria

Idiomas

Idioma Conversação Leitura Escrita Compreensão Peer-review
Inglês Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1)
Formação
Grau Classificação
2022/11/25
Concluído
 Investigação Clínica e em Serviços de Saúde (Doutoramento)
Especialização em Neuropediatria
Universidade do Porto Faculdade de Medicina, Portugal
"Stereotypies in Autism Spectrum Disorder" (TESE/DISSERTAÇÃO)
Percurso profissional

Docência no Ensino Superior

Categoria Profissional
Instituição de acolhimento 		Empregador
2023/08/23 - Atual Professor Auxiliar Convidado (Docente Universitário) Universidade do Porto Faculdade de Medicina, Portugal
Universidade do Porto Faculdade de Medicina, Portugal
Produções

Publicações

Artigo em revista
  1. Magalhães T; Melo C; Sampaio M; Correia-Costa A; Sousa R. "Hyperkinetic Movement Disorder in a Child.". Pediatrics in review (2023): https://doi.org/10.1542/pir.2021-005247.
    10.1542/pir.2021-005247
  2. Veronica Cabreira; Ferreira D; Melo C; Rebelo J; Fonseca J; Sousa R; Sampaio M. "Child Neurology: Anti-Hu Encephalitis in an Adolescent With a Mediastinal Seminoma.". Neurology (2023): https://doi.org/10.1212/WNL.0000000000207673.
    10.1212/wnl.0000000000207673
  3. Almeida AI; Sampaio L; Melo C; Sousa R. "Neuroimaging of poliomyelitis-like syndrome by Epstein-Barr virus.". Anales de pediatria (2023): https://doi.org/10.1016/j.anpede.2023.06.012.
    10.1016/j.anpede.2023.06.012
  4. Barreto-Mota R; Figueirinha J; Quental R; Fonseca J; Melo C; Sampaio M; Sousa R. "X-linked myotubular myopathy: a clinical report and a review of the mild phenotype.". Revista de neurologia (2023): https://europepmc.org/articles/PMC10478112.
    10.33588/rn.7607.2021447
  5. Joana Pereira Nunes; Sousa JM; Fonseca J; Melo C; Alves D; Sampaio M; Sousa R. "Successful Treatment of a Child With Epileptic Encephalopathy With Spike-Wave Activation in Sleep and GRIN2A Variant Using Sulthiame.". Cureus (2023): https://europepmc.org/articles/PMC9996194.
    10.7759/cureus.34686
  6. Cláudia Melo; Tiago Pinto Ribeiro; Catarina Prior; Camila Gesta; Vânia Martins; Guiomar Oliveira; Teresa Temudo. "Motor stereotypies in autism spectrum disorder: Clinical randomized study and classification proposal". Autism (2023): https://doi.org/10.1177/13623613221105479.
    10.1177/13623613221105479
  7. Gomes SM; Figueiredo R; Morais R; Soares S; Fonseca J; Melo C; Sampaio M; Sousa R. "Cerebral venous thrombosis in adolescence: Looking beyond the obvious.". International journal of pediatrics & adolescent medicine (2022): https://europepmc.org/articles/PMC10019955.
    10.1016/j.ijpam.2022.09.001
  8. Nogueira M; Melo C; Ana Grangeia; Magalhães T; Soares C; Dias R; Fonseca J; Sampaio M; Sousa R. "PURA syndrome in a child with severe developmental delay: a challenging diagnosis.". Revista de neurologia (2022): https://doi.org/10.33588/rn.7405.2021068.
    10.33588/rn.7405.2021068
  9. "Pediatric neuromyelitis optica spectrum disorders in Portugal: A multicentre retrospective study". Multiple Sclerosis and Related Disorders (2022): 103531-103531. http://dx.doi.org/10.1016/j.msard.2022.103531.
    10.1016/j.msard.2022.103531
  10. "Status epilepticus—Therapeutic management at the pediatric emergency department". Neurología (2021): http://dx.doi.org/10.1016/j.nrl.2021.09.009.
    10.1016/j.nrl.2021.09.009
  11. "Cyclic seizures in lethal neonatal rigidity and multifocal seizure syndrome: expanding the phenotype of a rare entity.". Epileptic disorders : international epilepsy journal with videotape (2021): https://doi.org/10.1684/epd.2021.1324.
    10.1684/epd.2021.1324
  12. "Neuromyelitis optica spectrum disorders: A nationwide Portuguese clinical epidemiological study.". Multiple sclerosis and related disorders (2021): https://doi.org/10.1016/j.msard.2021.103258.
    10.1016/j.msard.2021.103258
  13. "RHOBTB2 p.Arg511Trp Mutation in Early Infantile Epileptic Encephalopathy-64: Review and Case Report". Journal of Pediatric Genetics (2021): http://dx.doi.org/10.1055/s-0040-1722288.
    10.1055/s-0040-1722288
  14. "Ptosis, Areflexia and Ataxia in a 4-year-old Girl". Pediatrics In Review 42 Supplement (2021): S126-S128. http://dx.doi.org/10.1542/pir.2018-0357.
    10.1542/pir.2018-0357
  15. Cláudia Melo; Luís Ruano; Joana Jorge; Tiago Pinto Ribeiro; Guiomar Oliveira; Luís Azevedo; Teresa Temudo. "Prevalence and determinants of motor stereotypies in autism spectrum disorder: A systematic review and meta-analysis". Autism (2020): 136236131986911-136236131986911. https://doi.org/10.1177/1362361319869118.
    10.1177/1362361319869118
  16. "Guillain-Barré Syndrome in a Teenage Girl: A Severe Case With Anti-GM2 Antibodies Associated With Acute CMV Infection and Literature Review". Clinical Pediatrics 59 3 (2020): 300-304. http://dx.doi.org/10.1177/0009922819898186.
    10.1177/0009922819898186
  17. "Neuroimagen en la encefalitis por virus Epstein-Barr". Anales de Pediatría 92 1 (2020): 53-54. http://dx.doi.org/10.1016/j.anpedi.2018.09.016.
    10.1016/j.anpedi.2018.09.016
  18. "Hypotonia and feeding problems in the newborn: a congenital myotonic dystrophy type 1 clinical case". NASCER E CRESCER - BIRTH AND GROWTH MEDICAL JOURNAL (2019): Vol 27 No 4 (2018)-Vol 27 No 4 (2018). https://revistas.rcaap.pt/nascercrescer/article/view/12046.
    10.25753/BIRTHGROWTHMJ.V27.I4.12046
  19. "Acute Ischemic Stroke in a Child Successfully Treated with Thrombolytic Therapy and Mechanical Thrombectomy.". Case reports in neurology (2019): https://europepmc.org/articles/PMC6739694.
    10.1159/000496535
  20. "Child Neurology: Treatable bilateral striatal lesions related to anti-dopamine 2 receptor autoimmunity". Neurology 91 2 (2018): 98-101. http://dx.doi.org/10.1212/wnl.0000000000005774.
    10.1212/wnl.0000000000005774
  21. "Claustrum sign in a child with refractory status epilepticus after febrile illness: why does it happen?". Acta Neurologica Belgica 118 2 (2018): 303-305. http://dx.doi.org/10.1007/s13760-017-0820-9.
    10.1007/s13760-017-0820-9
  22. "Lyme disease and juvenile idiopathic arthritis – A pediatric case report". Revista Brasileira de Reumatologia (English Edition) 57 6 (2017): 620-622. http://dx.doi.org/10.1016/j.rbre.2015.09.006.
    10.1016/j.rbre.2015.09.006
  23. "Clinical practices among healthcare professionals concerning neonatal jaundice and pale stools". European Journal of Pediatrics 176 3 (2017): 361-369. http://dx.doi.org/10.1007/s00431-016-2847-y.
    10.1007/s00431-016-2847-y
  24. "Erythema dyschromicum perstans in a child following an enteroviral meningitis". Anais Brasileiros de Dermatologia 92 1 (2017): 137-138. http://dx.doi.org/10.1590/abd1806-4841.201745144.
    10.1590/abd1806-4841.201745144
  25. "Stereotypies: From Normal to Pathological". Journal of Pediatric Neurology 13 04 (2015): 208-212. http://dx.doi.org/10.1055/s-0035-1559805.
    10.1055/s-0035-1559805
  26. "Alpha-1-Antitrypsin Deficiency Presenting as Neonatal Cholestasis: Predictors of Outcome and Effect of Ursodeoxycholic Acid". Journal of Liver 04 04 (2015): http://dx.doi.org/10.4172/2167-0889.1000185.
    10.4172/2167-0889.1000185
  27. "The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.". Neuroepidemiology (2014): https://doi.org/10.1159/000358801.
    10.1159/000358801
  28. "Cat eye syndrome and growth hormone deficiency with pituitary anomalies: A case report and review of the literature". Gene 529 1 (2013): 186-189. http://dx.doi.org/10.1016/j.gene.2013.07.031.
    10.1016/j.gene.2013.07.031