???global.info.a_carregar???
Identification

Personal identification

Full name
Ruben Rocha

Citation names

  • Rocha, Ruben

Author identifiers

Ciência ID
731B-8049-FA18
ORCID iD
0000-0002-5523-538X
Education
Degree Classification
2015
Concluded
 Neurociências (Doutoramento)
Major in Área de especialidade: Neurociências Clínicas, Neuropsiquiatria e Saúde Mental
Universidade do Porto Faculdade de Medicina, Portugal
"HYPOXIA-ISCHEMIA IN NEONATAL BRAIN: A TRANSLATIONAL APPROACH TO ITS CONSEQUENCES" (THESIS/DISSERTATION)
Affiliation

Other Careers

Category
Host institution 		Employer
2021/04/01 - Current Assistente graduado (Médica) Centro Hospitalar Universitário de São João, Portugal
Centro Hospitalar Universitário de São João, Portugal
2017/01/01 - 2021/03/31 Assistente (Médica) Centro Hospitalar Universitário do Porto EPE Centro Materno-Infantil do Norte Dr Albino Aroso, Portugal
Centro Hospitalar Universitário do Porto EPE Centro Materno-Infantil do Norte Dr Albino Aroso, Portugal
2012/01/01 - 2016/12 Assistente (Médica) Centro Hospitalar Universitário de São João, Portugal
Projects

Contract

Designation Funders
2019/01/01 - 2019/12/31 Centro de Investigação em Tecnologias e Serviços de Saúde
UID/IC/04255/2019
Universidade do Porto Faculdade de Medicina, Portugal

Centro de Investigação em Tecnologias e Serviços de Saúde, Portugal

Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal

Escola Superior de Enfermagem do Porto, Portugal

Universidade de Aveiro, Portugal
Fundação para a Ciência e a Tecnologia
Concluded
Outputs

Publications

Journal article
  1. Figueiredo, Rafael Costa; Rocha, Ruben; Freitas Baptista , Cristina; Santos, Manuela; Figueiroa , Sónia; Carrilho, Inês; Temudo, Teresa. "Dravet Syndrome - experience of a Neuropediatric Unit". (2021): https://revistas.rcaap.pt/nascercrescer/article/view/21347.
  2. Figueiredo Costa, Marcos; Rocha, Ruben; Baptista, Cristina Freitas; Santos, Manuela; Figueiroa, Sónia; Carrilho, Inês; Temudo, Teresa. "Dravet Syndrome - experience of a Neuropediatric Unit". (2021): http://hdl.handle.net/10400.16/2750.
    https://doi.org/10.25753/BirthGrowthMJ.v30.i4.21347
  3. Figueiredo,Rafael; Rocha,Ruben; Baptista,Cristina Freitas; Santos,Manuela; Figueiroa,Sónia; Carrilho,Inês; Temudo,Teresa. "Dravet Syndrome - experience of a neuropediatric unit". (2021): http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542021000400213.
  4. "Epilepsy in paediatric patients with Parry-Romberg syndrome: A review of the literature.". Seizure (2020): https://doi.org/10.1016/j.seizure.2020.01.017.
    10.1016/j.seizure.2020.01.017
  5. Rocha, Ruben; Kaliakatsos, Marios. "Epilepsy in paediatric patients with Parry-Romberg syndrome: A review of the literature". (2020): http://hdl.handle.net/10400.16/2719.
    10.1016/j.seizure.2020.01.017
  6. Azevedo Alves, Raquel; Lopes, Marta; Rocha, Ruben; Carrilho, Inês. "Treatment of acute migraine and status migrainosus in pediatrics". (2019): https://doi.org/10.25753/BirthGrowthMJ.v28.i3.15431.
    https://doi.org/10.25753/BirthGrowthMJ.v28.i3.15431
  7. Alves,Raquel Azevedo; Lopes,Marta; Rocha,Ruben; Carrilho,Inês. "Treatment of acute migraine and status migrainosus in pediatrics". (2019): http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542019000300004.
  8. Rocha H; Sampaio M; Rocha R; Fernandes S; Leão M. "MEF2C haploinsufficiency syndrome: Report of a new MEF2C mutation and review.". (2016): http://europepmc.org/abstract/med/27255693.
    10.1016/j.ejmg.2016.05.017
  9. Sampaio L; Dias da Costa JM; Rocha R; Leão M. "Brain Herniation into the Dural Venous Sinus.". (2016): http://europepmc.org/abstract/med/27174142.
    10.1016/j.jpeds.2016.04.010
  10. Sampaio M; Rocha R; Biskup S; Leão M. "Novel STXBP1 mutations in 2 patients with early infantile epileptic encephalopathy.". (2015): http://europepmc.org/abstract/med/23533165.
    10.1177/0883073813479169
  11. Gonçalves D; Meireles J; Rocha R; Sampaio M; Leão M. "Syndrome of transient headache and neurologic deficits with cerebrospinal fluid lymphocytosis (HaNDL): a pediatric case report.". (2013): http://europepmc.org/abstract/med/23076427.
    10.1177/0883073812462063
  12. Corujeira S; Águeda S; Monteiro G; Canelhas A; Sampaio M; Rocha R; Leão M. "Expanding the phenotype of IFAP/BRESECK syndrome: a new case with severe hypogammaglobulinemia.". (2013): http://europepmc.org/abstract/med/24090718.
    10.1016/j.ejmg.2013.09.005
  13. Rocha R; Lisboa L; Neves J; García López M; Santos E; Ribeiro A. "Neuroborreliosis presenting as acute disseminated encephalomyelitis.". (2012): http://europepmc.org/abstract/med/23222106.
    10.1097/pec.0b013e318276c51d
  14. Rocha R; Soro I; Leitão A; Silva ML; Leão M. "Moyamoya vascular pattern in Alagille syndrome.". (2012): http://europepmc.org/abstract/med/22759690.
    10.1016/j.pediatrneurol.2012.04.014
  15. Rocha R; Vitor AB; Trindade E; Lima R; Tavares M; Lopes J; Dias JA. "Omalizumab in the treatment of eosinophilic esophagitis and food allergy.". (2011): http://europepmc.org/abstract/med/21809010.
    10.1007/s00431-011-1540-4
  16. Antunes H; Rocha R; Silva N; Pontes T; Antunes A; Martins S. "Immune disease expressed in liver and platelets in an adolescent: a case report.". (2010): http://europepmc.org/abstract/med/20540743.
    10.1186/1824-7288-36-42
  17. Antunes, Henedina; Rocha, Ruben; Silva, Nicole; Pontes, Teresa; Antunes, Ana; Martins, Sofia. "Immune disease expressed in liver and platelets in an adolescent: a case report". (2010): http://hdl.handle.net/1822/29341.
    10.1186/1824-7288-36-42
  18. Ferreira S; Almeida R; Guerrero H; Lourenço-Ferreira S; Fonseca L; Rocha R; Rocha-Gonçalves F; Ferreira A; Bettencourt P. "Prognosis of decompensated heart failure: role of NT-proBNP.". (2007): http://europepmc.org/abstract/med/17691279.
Thesis / Dissertation
  1. Rúben Sá Balão Alves da Rocha. "HYPOXIA-ISCHEMIA IN NEONATAL BRAIN: A TRANSLATIONAL APPROACH TO ITS CONSEQUENCES". PhD, 2023. https://hdl.handle.net/10216/151136.

Other

Other output
  1. A presumed tubercular choroiditis based on interferon-gamma release assay and response to therapy. [Excerpt] Ocular tuberculosis is a rare and a typical manifestation of Mycobacterium tuberculosis infection. Quite often the confirmation of the diagnosis is difficult and conventional approach to diagnosis and management is not enough. [...]. (undefined). 2010. Rocha, Ruben; Martins, Sofia; Ferreira, Carla; Antunes, Henedina. http://hdl.handle.net/1822/67557.
    10.1097/INF.0b013e3181ecc286