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Mostrar 97-105 de um total de 105 resultados. < anterior 
DataTítuloAutor(es)TipoAcesso
18-Out-2012Therapeutic strategies for polyQ diseases: from cellular and animal models to the clinicSilva, Sara Carina Duarte; Jalles, Ana; Maciel, P.Capítulo de livroAcesso restrito UMinho
2005Towards a structural understanding of the fibrillization pathway in Machado-Joseph’s disease: trapping early oligomers of non-expanded ataxin-3Gales, Luís; Cortes, Luísa; Almeida, Carla, et al.ArtigoAcesso aberto
7-Fev-2023Transition from animal-based to human induced pluripotent stem cells (iPSCs)-based models of neurodevelopmental disorders: opportunities and challengesGuerreiro, Sara Francisca Ramalhosa; Maciel, P.ArtigoAcesso aberto
Mar-2010Trastornos nutricionales y gastrointestinales en el síndrome de Rett: importancia de la intervención tempranaPrior, C.; Nunes, A.; Rios, M., et al.ArtigoAcesso restrito autor
2020Unravelling the anticancer potential of functionalized chromeno[2,3-b ] pyridines for breast cancer treatmentOliveira-Pinto, Sofia; Pontes, Olivia; Lopes, Diogo, et al.ArtigoAcesso restrito UMinho
Mar-2013Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disordersBessa, C.; Maciel, P.; Rodrigues, Ana JoãoArtigoAcesso aberto
10-Nov-2015Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 geneVieira, José Pedro; Lopes, Fátima Daniela Teixeira; Fernandes, Anabela Silva, et al.ArtigoAcesso aberto
Out-2017Whole gene deletion of EBF3 supporting haploinsufficiency of this gene as a mechanism of neurodevelopmental diseaseLopes, Fátima Daniela Teixeira; Soares, Gabriela; Rocha, Miguel Gonçalves, et al.ArtigoAcesso aberto
2003A whole genome screen for association with multiple sclerosis in portuguese patientsSantos, M.; Pinto-Basto, J.; Rio, M. E., et al.ArtigoAcesso aberto