1
TITLE: PURA syndrome in a child with severe developmental delay: a challenging diagnosis
AUTHORS: Nogueira, M; Melo, C ; Grangeia, A; Magalhaes, T; Soares, C; Dias, R; Fonseca, J; Sampaio, M; Sousa, R;
PUBLISHED: 2022, SOURCE: REVISTA DE NEUROLOGIA, VOLUME: 74, ISSUE: 5
INDEXED IN: WOS
2
TITLE: PURA syndrome in a child with severe developmental delay: A challenging diagnosis [Síndrome PURA en una niña con retraso grave del desarrollo: Un diagnóstico desafiante]
AUTHORS: Nogueira, M; Melo, C ; Grangeia, A ; Magalhães, T; Soares, C; Dias, R; Fonseca, J ; Sampaio, M; Sousa, R;
PUBLISHED: 2022, SOURCE: Revista de Neurologia, VOLUME: 74, ISSUE: 5
INDEXED IN: Scopus CrossRef
3
TITLE: Cyclic seizures in lethal neonatal rigidity and multifocal seizure syndrome: expanding the phenotype of a rare entity
AUTHORS: Vanessa Gorito; Helena Rocha; Cláudia Melo ; Jacinta Fonseca; Marta Pinheiro; Cristina Ferreras; Miguel Leão; Mafalda Sampaio; Dílio Alves; Raquel Sousa;
PUBLISHED: 2021, SOURCE: Epileptic Disorders, VOLUME: 23, ISSUE: 5
INDEXED IN: CrossRef
IN MY: ORCID
4
TITLE: Cyclic seizures in lethal neonatal rigidity and multifocal seizure syndrome: expanding the phenotype of a rare entity
AUTHORS: Gorito, V; Rocha, H; Melo, C ; Fonseca, J; Pinheiro, M; Ferreras, C; Leao, M; Sampaio, M; Alves, D; Sousa, R;
PUBLISHED: 2021, SOURCE: EPILEPTIC DISORDERS, VOLUME: 23, ISSUE: 5
INDEXED IN: WOS
5
TITLE: Cyclic seizures in lethal neonatal rigidity and multifocal seizure syndrome: expanding the phenotype of a rare entity
AUTHORS: Gorito, V; Rocha, H; Melo, C ; Fonseca, J ; Pinheiro, M; Ferreras, C; Leao, M; Sampaio, M; Alves, D; Sousa, R;
PUBLISHED: 2021, SOURCE: EPILEPTIC DISORDERS, VOLUME: 23, ISSUE: 5
INDEXED IN: Scopus WOS Unpaywall
6
TITLE: Neuromyelitis optica spectrum disorders: A nationwide Portuguese clinical epidemiological study  Full Text
AUTHORS: Santos, E; Rocha, AL; Oliveira, V; Ferro, D; Samo, R; Sousa, AP; Figueiroa, S; Mendonca, T; Abreu, P; Guimaraes, J; Sousa, R; Melo, C ; Correia, I; Duraes, J; Sousa, L; Ferreira, J; de Sa, J; Sousa, F; Sequeira, M; Correia, AS; Andre, AL; Basilio, C; Arenga, M; Mendes, I; Marques, IB; Perdigao, S; Felgueiras, H; Alves, I; Correia, F; Barroso, C; Morganho, A; Carmona, C; Palavra, F; Santos, M ; Salgado, V; Palos, A; Nzwalo, H; Timoteo, A; Guerreiro, R; Isidoro, L; Boleixa, D; Carneiro, P; Neves, E; Silva, AM; Goncalves, G; Leite, MI; Sa, MJ; ...More
PUBLISHED: 2021, SOURCE: MULTIPLE SCLEROSIS AND RELATED DISORDERS, VOLUME: 56
INDEXED IN: WOS CrossRef: 6
IN MY: ORCID
7
TITLE: Pediatric neuromyelitis optica spectrum disorders in Portugal  Full Text
AUTHORS: Martins, C; Figueiroa, S; Garrido, C; Martins, J; Samoes, R; Guimaraes, J; Sousa, R; Melo, C ; Palavra, F; Ferreira, J; Silva, AM; Sa, M; Santos, E;
PUBLISHED: 2021, SOURCE: EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 28
INDEXED IN: WOS CrossRef: 2
IN MY: ORCID
8
TITLE: Ptosis, Areflexia and Ataxia in a 4-year-old Girl
AUTHORS: Ferreira, SH; Lopes, C; Abreu, M; Melo, C ; Alves, D; Soares, R;
PUBLISHED: 2021, SOURCE: Pediatrics in review, VOLUME: 42, ISSUE: Supplement_1
INDEXED IN: Scopus CrossRef
IN MY: ORCID
9
TITLE: RHOBTB2 p.Arg511Trp Mutation in Early Infantile Epileptic Encephalopathy-64: Review and Case Report
AUTHORS: Fonseca, J ; Melo, C ; Ferreira, C; Sampaio, M; Sousa, R; Leao, M;
PUBLISHED: 2021, SOURCE: JOURNAL OF PEDIATRIC GENETICS
INDEXED IN: WOS CrossRef Unpaywall
IN MY: ORCID
10
TITLE: Status epilepticus—Therapeutic management at the pediatric emergency department
AUTHORS: Pais-Cunha, I; Valente, D; D.B Abreu; Fonseca, J; Melo, C ; Sampaio, M; L.A Santos; Sousa, R;
PUBLISHED: 2021, SOURCE: Neurología
INDEXED IN: CrossRef
IN MY: ORCID
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