Percorrer por assunto Rett Syndrome

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Mostrar 1-12 de um total de 12 resultados.
DataTítuloAutor(es)TipoAcesso
Nov-2007Abnormal movements in Rett syndrome are present before the regression period: a case studyTemudo, Teresa; Maciel, P.; Sequeiros, JorgeArtigoAcesso restrito UMinho
Ago-2007An explanation for another familial case of Rett syndrome: maternal germline mosaicismVenâncio, Margarida; Santos, Mónica; Pereira, Susana Aires, et al.ArtigoAcesso aberto
2008Analysis 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 retardationSantos, Mónica; Yan, Jin; Temudo, Teresa, et al.ArtigoAcesso restrito UMinho
15-Mar-2008Atypical stereotypies and vocal tics in Rett syndrome: an illustrative caseTemudo, Teresa; Freitas, Paula; Sequeiros, Jorge, et al.Carta ao editorAcesso restrito UMinho
2006Chromatin remodeling and neuronal function: exciting linksSantos, Monica; Coelho, P. A.; Maciel, P.ArtigoAcesso aberto
Jan-2009Evaluation of CSF neurotransmitters and folate in 25 patients with Rett disorder and effects of treatmentTemudo, T.; Rios, M.; Prior, C., et al.ArtigoAcesso aberto
Abr-2007Evidence for abnormal early development in a mouse model of Rett syndromeSantos, Mónica; Silva-Fernandes, Anabela; Oliveira, P., et al.ArtigoAcesso restrito UMinho
13-Out-2010Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndromeSantos, M.; Summavielle, T.; Teixeira-Castro, A., et al.ArtigoAcesso restrito UMinho
30-Jul-2008Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation typeTemudo, Teresa; Ramos, Elisabete; Dias, Karin, et al.ArtigoAcesso restrito UMinho
Jan-2009Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patientsSantos, Mónica; Temudo, Teresa; Kay, Teresa, et al.ArtigoAcesso aberto
Abr-2007Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutationsTemudo, T.; Oliveira, P.; Santos, M., et al.ArtigoAcesso restrito UMinho
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