Collection's Items (Sorted by Submit Date in Descending order): 21 to 40 of 94
| Issue Date | Title | Author(s) | Type | Access Type |
| Oct-2008 | Ophthalmoplegic Migraine and Infundibular Dilatation of a Cerebral Artery | Vieira, JP; Castro, J; Gomes, LB; Jacinto, S; Dias, AI | article |  |
| 2001 | Non-Progressive Leukoencephalopathy with Bilateral Temporal Cysts | Gomes, AL; Vieira, JP; Saldanha, J | 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 | |
| 2006 | Short-Lasting Headaches in Children | Vieira, JP; Salgueiro, AB; Alfaro, M | article | |
| 2006 | Epilepsy and Deletions at Chromosome 2q24 | Pereira, S; Vieira, JP; Cau, P; Genton, P; Szepetowski, P | article | |
| 2008 | Analysis of Highly Conserved Regions of the 3'UTR of MECP2 Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation | Santos, M; Yan, J; Temudo, T; Oliveira, G; Vieira, JP; Fen, J; Sommer, S; Maciel, P | article | |
| 2009 | Evaluation of CSF Neurotransmitters and Folate in 25 Patients with Rett Disorder and Effects of Treatment | Temudo, T; Rios, M; Prior, C; Carrilho, I; Santos, M; Maciel, P; Sequeiros, J; Fonseca, M; Monteiro, J; Cabral, P; Vieira, JP; Ormazabal, A; Artuch, R | 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 | |
| 2015 | Variant Rett Syndrome in a Girl with a Pericentric X-Chromosome Inversion Leading to Epigenetic Changes and Overexpression of the MECP2 Gene | Vieira, JP; Lopes, F; Silva-Fernandes, A; Sousa, MV; Moura, S; Sousa, S; Costa, BM; Barbosa, M; Ylstra, B; Temudo, T; Lourenço, T; Maciel, P | article | |
| 2014 | Gain-of-Function Mutations in IFIH1 Cause a Spectrum of Human Disease Phenotypes Associated with Upregulated Type I Interferon Signaling | Rice, G; Toro Duany, Y; Jenkinson, E; Forte, G; Anderson, B; Ariaudo, G; Bader-Meunier, B; Baildam, E; Battini, R; Beresford, M; Casarano, M; Chouchane, M; Cimaz, R; Collins, AM; Cordeiro, N; Dale, R; Davidson, J; De Waele, L; Desguerre, I; Faivre, L; Fazzi, E; Isidor, B; Lagae, L; Latchman, A; Lebon, P; Li, C; Livingston, J; Lourenço, C; Mancardi, MM; Masurel-Paulet, A; McInnes, I; Menezes, M; Mignot, C; O’Sullivan, J; Orcesi, S; Picco, P; Riva, E; Robinson, R; Rodriguez, D; Salvatici, E; Scott, C; Szybowska, M; Tolmie, J; Vanderver, A; Vanhulle, C; Vieira, JP; Webb, K; Whitney, R; Williams, S; Wolfe, L; M Zuberi, S; Hur, S; Crow, Y | article | |
| 2006 | Neurocisticercose em Idade Pediátrica | Ferreira, M; Brito, MJ; Vieira, JP; Salgueiro, AB; Machado, MC | article | |
| 2000 | Hiperglicinémia Não Cetótica: A Propósito de Dois Casos Tratados com Dextrometorfano e Benzoato de Sódio | Pereira-da-Silva, L; Carvalho, A; Videira-Amaral, J; Sequeira, S; Cabral, P; Gonçalves, H; Serrano, A; Galha, H; Cabral, A | article | |
| 2000 | Encefalite Crónica a Enterovírus num Doente com Agamaglobulinémia Congénita Ligada ao Cromossoma X | Dias, AI; Alves, A; Fialho, M; Martins, M; Cabral, P | article | |
| 1999 | Diagnóstico Pré-Natal das Anomalias do Tracto Urinário e Valor da Cistografia Miccional no Estudo Evolutivo Pós-Natal | Batista, J; Abranches, M; Silva, A; Tavares, MN; Ferra de Sousa, J; Videira-Amaral, J | article | |
| 1997 | Hemiplegia Alternante da Infância. A Propósito de Um Caso Clínico | Dias, K; Moreno, T | article | |
| 2011 | Síndrome de Guillain-Barré em Idade Pediátrica. Protocolo de Actuação | Sampaio, MJ; Figueiroa, S; Temudo, T; Gomes, S; Janeiro, P; Silva, R | article | |
| 2013 | Torcicolo Adquirido na Criança | Regala, J; Martins, J; Dias, AI; Moreira, A; Cassiano Neves, M | article | |
| 2001 | Clinical and Molecular Findings in Four New Patients Harbouring the mtDNA 8993T C Mutation | Vilarinho, L; Carrozzo, R; Barbot, C; Calado, E; Tessa, A; Dionisi-Vici, C; Guimarães, A; Santorelli, FM | article | |
| 2013 | Botulismo Infantil em Portugal – Um Lactente com Hipotonia | Malveiro, D; Henriques, C; Flores, P; Barata, D; Vieira, JP; Cabral, P | article | |
| 2006 | Craniossinostoses Importância Clínica e Implicações Funcionais | Cristovão, C; Emílio, A; Soares, MR; Dias, AI; Matos, M; Távora, L | article | |
Collection's Items (Sorted by Submit Date in Descending order): 21 to 40 of 94
