Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE: Search

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Issue Date	Title	Author(s)	Type	Access Type
Jan-2009	Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients	Santos, M; Temudo, T; Kay, T; Carrilho, I; Medeira, A; Cabral, H; Gomes, R; Lourenço, T; Venâncio, M; Calado, E; Moreira, A; Oliveira, G; Maciel, P	article
2016	Diplopia, Convergent Strabismus, and Eye Abduction Palsy in a 12-Year-Old Boy with Autoimmune Thyroiditis	Marques, P; Jacinto, S; Pinto, MC; Limbert, C; Lopes, L	article
2011	Rett Syndrome With and Without Detected MECP2 Mutations: an Attempt to Redefine Phenotypes	Temudo, 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, P	article
2006	Short-Lasting Headaches in Children	Vieira, JP; Salgueiro, AB; Alfaro, M	article
Sep-2006	The BOLD Effect of Interictal Spike Activity in Childhood Occipital Lobe Epilepsy	Leal, A; Dias, AI; Vieira, JP; Secca, M; Jordão, C	article
Sep-2003	Different Electroclinical Manifestations of the Epilepsy Associated with Hamartomas Connecting to the Middle or Posterior Hypothalamus	Leal, A; Moreira, A; Robalo, C; Ribeiro, C	article
1-Mar-2017	Epileptic Spasms in Congenital Disorders of Glycosylation	Pereira, AG; Bahi-Buisson, N; Barnerias, C; Boddaert, N; Nabbout, R; de Lonlay, P; Kaminska, A; Eisermann, M	article
Dec-2002	The "Failures" of Spina Bifida Transdisciplinary Care	Calado, E; Loff, C	article
Aug-2010	Fractures in Children and Adolescents with Spina Bifida: The Experience of a Portuguese Tertiary-Care Hospital	Marreiros, H; Monteiro, L; Loff, C; Calado, E	article
2018	Mental Nerve Neuropathy: A Rare Manifestation in Sickle Cell Disease	Alcafache, M; Santos, S; Sassetti, M; Batalha, S; Maia, R; Lopes da Silva, R; Kjöllerström, P	article