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Results 1-10 of 15 (Search time: 0.004 seconds).
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Issue DateTitleAuthor(s)TypeAccess Type
Jan-2009Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male PatientsSantos, M; Temudo, T; Kay, T; Carrilho, I; Medeira, A; Cabral, H; Gomes, R; Lourenço, T; Venâncio, M; Calado, E; Moreira, A; Oliveira, G; Maciel, ParticleopenAccess
May-2014Autism Spectrum Disorder Secondary to Enterovirus EncephalitisMarques, F; Brito, MJ; Conde, M; Pinto, M; Moreira, AarticleopenAccess
2005Neurofibromatose do Tipo 1 - Proposta de Protocolo de SeguimentoAnselmo, M; Calado, E; Vieira, JP; Dias, AI; Moreira, A; Dias, KarticleopenAccess
2005Défice de Ciclohidrolase (Distonia Dopa Sensìvel) Autossómica Dominante.Manita, M; Moreira, A; Calado, E; Vilarinho, LarticleopenAccess
2008Síndrome de Jeavons: Uma Entidade Clínica Independente?Borges, D; Calado, E; Moreira, A; Cabral, P; Seabra, A; Dlas, AIarticleopenAccess
2013Torcicolo Adquirido na CriançaRegala, J; Martins, J; Dias, AI; Moreira, A; Cassiano Neves, MarticleopenAccess
2011Rett Syndrome With and Without Detected MECP2 Mutations: an Attempt to Redefine PhenotypesTemudo, T; Santos, M; Ramos, E; Dias, K; Vieira, JP; Moreira, A; Calado, E; Carrilho, I; Oliveira, G; Levy, A; Barbot, C; Fonseca, M; Cabral, A; Cabral, P; Monteiro, J; Borges, L; Gomes, R; Mira, G; Pereira, SA; Santos, M; Fernandes, A; Epplen, JT; Sequeiros, J; Maciel, ParticleopenAccess
Sep-2003Different Electroclinical Manifestations of the Epilepsy Associated with Hamartomas Connecting to the Middle or Posterior HypothalamusLeal, A; Moreira, A; Robalo, C; Ribeiro, CarticleopenAccess
Jun-2017Hyperprolinemia as a Clue in the Diagnosis of a Patient with Psychiatric ManifestationsDuarte, M; Afonso, J; Moreira, A; Antunes, D; Ferreira, C; Correia, H; Marques, M; Sequeira, SarticleopenAccess
2007Analysis of the Generators of Epileptic Activity in Early-Onset Childhood Benign Occipital Lobe EpilepsyLeal, A; Nunes, S; Dias, AI; Vieira, JP; Moreira, A; Calado, EarticleopenAccess