1. Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE

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Issue DateTitleAuthor(s)TypeAccess Type
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
2006Short-Lasting Headaches in ChildrenVieira, JP; Salgueiro, AB; Alfaro, MarticleopenAccess
Sep-2006The BOLD Effect of Interictal Spike Activity in Childhood Occipital Lobe EpilepsyLeal, A; Dias, AI; Vieira, JP; Secca, M; Jordão, CarticleopenAccess
Dec-2002The "Failures" of Spina Bifida Transdisciplinary CareCalado, E; Loff, CarticleopenAccess
Sep-2003Different Electroclinical Manifestations of the Epilepsy Associated with Hamartomas Connecting to the Middle or Posterior HypothalamusLeal, A; Moreira, A; Robalo, C; Ribeiro, CarticleopenAccess
Aug-2010Fractures in Children and Adolescents with Spina Bifida: The Experience of a Portuguese Tertiary-Care HospitalMarreiros, H; Monteiro, L; Loff, C; Calado, EarticleopenAccess
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
2016Diplopia, Convergent Strabismus, and Eye Abduction Palsy in a 12-Year-Old Boy with Autoimmune ThyroiditisMarques, P; Jacinto, S; Pinto, MC; Limbert, C; Lopes, LarticleopenAccess
1-Mar-2017Epileptic Spasms in Congenital Disorders of GlycosylationPereira, AG; Bahi-Buisson, N; Barnerias, C; Boddaert, N; Nabbout, R; de Lonlay, P; Kaminska, A; Eisermann, MarticleopenAccess

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