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DataTítuloAutor(es)TipoAcesso
2005Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR)Shi, Jinxiu; Shibayama, Akane; Liu, Qiang, 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
2004Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese originSantos, Mónica; Costa, Maria do Carmo; Rio, Maria Edite, et al.ArtigoAcesso aberto
Jun-2007MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patientsCoutinho, Ana M.; Oliveira, Guiomar; Katz, Cécile, 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
2006Processes : working group reportChatty, Stéphane; Campos, J. Creissac; González, María Paula, et al.Artigo em ata de conferênciaAcesso aberto
Jan-2011Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypesTemudo, Teresa; Santos, Mónica; Ramos, Elisabete, et al.ArtigoAcesso aberto
2008The C677T polymorphism in MTHFR is not associated with migraine in PortugalFerro, Anabela; Castro, Maria-José; Lemos, Carolina, et al.ArtigoAcesso aberto
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