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Items da Coleção (Ordenados por Data de depósito em ordem descendente): 1 até 16 de 16
DataTítuloAutor(es)TipoAcesso
2013Bactérias Multirresistentes Associadas aos Cuidados de Saúde num Hospital Pediátrico: Experiência de Cinco Anos Cuidados de Saúde num Hospital Pediátrico: Experiência de Cinco AnosMação, P; Lopes, JC; Oliveira, H; Oliveira, G; Rodrigues, FarticleopenAccess
2014Autism Spectrum Disorder: FRAXE Mutation, a Rare EtiologyCorreia, F; Café, C; Almeida, J; Mouga, S; Oliveira, GarticleopenAccess
2014The impact of the metabotropic glutamate receptor and other gene family interaction networks on the autism spectrum disordersHadley, D; Wu, ZL; Kao, C; Kini, A; Mohamed-Hadley, A; AGP Consortium; Oliveira, G; et alarticleopenAccess
2014Convergence of genes and cellular pathways dysregulated in autism spectrum disordersPinto, D; Delaby, E; Merico, D; Barbosa, M; Merikangas, A; Oliveira, G; et alarticleopenAccess
2014Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCorreia, CT; Conceição, IC; Oliveira, B; Coelho, J; Sousa, I; Sequeira, AF; Almeida, J; Café, C; Duque, F; Mouga, S; Roberts, W; Gao, K; Lowe, JK; Thiruvahindrapuram, B; Walker, S; Marshall, CR; Pinto, D; Geschwind, JI; Scherer, SW; Oliveira, G; Vicente, AMarticleopenAccess
2012Síndromes de Deficiência Cerebral de CreatinaMalheiro, R; Diogo, L; Garcia, P; Fineza, I; Oliveira, GarticleopenAccess
2012Pediatria do neurodesenvolvimento: levantamente nacional de recursos e necessidadesOliveira, G; Duque, F; Duarte, C; Melo, F; Teles, L; Brito, F; Vale, MC; Guimarães, MJ; Gouveia, RarticleopenAccess
2012Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum DisordersLeblond, CS; Heinrich, J; Delorme, R; Proepper, C; Betancur, C; Huguet, G; Konyukh, M; Chaste, P; Oliveira, GarticleopenAccess
2012CNVs leading to fusion transcripts in individuals with autism spectrum disorderHolt, R; Sykes, NH; Conceição, IC; Cazier, JB; Anney, RJ; Oliveira, G; Gallagher, L; Monaco, AP; Pagnamenta, ATarticleopenAccess
2012A Direct Comparison of Local-Global Integration in Autism and other Developmental Disorders: Implications for the Central Coherence HypothesisBernardiono, I; Mouga, S; Almeida, J; van Asselen, M; Oliveira, GarticleopenAccess
2010Paralisia do plexo braquial no recém-nascido: experiência de dez anos numa Maternidade de Apoio Perinatal DiferenciadoSilva, S; Mimoso, G; Gonçalves, O; Araújo, HarticleopenAccess
2008A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopiaGilling, M; Lauritsen, MB; Møller, M; Henriksen, KF; Vicente, A; Oliveira, G; Cintin, C; Eiberg, H; Andersen, PS; Mors, O; Rosenberg, T; Brøndum-Nielsen, K; Cotterill, RM; Lundsteen, C; Ropers, HH; Ullmann, R; Bache, I; Tümer, Z; Tommerup, NarticleopenAccess
2008Genome-wide linkage analyses of quantitative and categorical autism subphenotypesLiu, XQ; Paterson, AD; Szatmari, P; Oliveira, G; Autism Genome Project ConsortiumarticleopenAccess
2009A genome-wide linkage and association scan reveals novel loci for autismWeiss, LA; Arking, DE; Daly, MJ; Chakravarti, A; Oliveira, G; Gene Discovery Project of Johns Hopkins & the Autism ConsortiumarticleopenAccess
2010A genome-wide scan for common alleles affecting risk for autismAnney, R; Klein, L; Pinto, D; Pegan, R; Magalhães, TR; Almeida, J; Oliveira, GarticleopenAccess
2009Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boyCarreira, IM; Melo, JB; Rodrigues, C; Backx, L; Vermeesch, J; Weise, A; Kosyakova, N; Oliveira, G; Matoso, EarticleopenAccess
Items da Coleção (Ordenados por Data de depósito em ordem descendente): 1 até 16 de 16