Data | Título | Autor(es) | Tipo | Acesso |
Ago-2007 | An explanation for another familial case of Rett syndrome: maternal germline mosaicism | Venâncio, Margarida; Santos, Mónica; Pereira, Susana Aires, et al. | Artigo | Acesso aberto |
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, Mónica; Yan, Jin; Temudo, Teresa, et al. | Artigo | Acesso restrito UMinho |
2005 | Detection 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. | Artigo | Acesso aberto |
Abr-2007 | Evidence for abnormal early development in a mouse model of Rett syndrome | Santos, Mónica; Silva-Fernandes, Anabela; Oliveira, P., et al. | Artigo | Acesso restrito UMinho |
2004 | Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin | Santos, Mónica; Costa, Maria do Carmo; Rio, Maria Edite, et al. | Artigo | Acesso aberto |
Jun-2007 | MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients | Coutinho, Ana M.; Oliveira, Guiomar; Katz, Cécile, et al. | Artigo | Acesso restrito UMinho |
Jan-2009 | Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients | Santos, Mónica; Temudo, Teresa; Kay, Teresa, et al. | Artigo | Acesso aberto |
2006 | Processes : working group report | Chatty, Stéphane; Campos, J. Creissac; González, María Paula, et al. | Artigo em ata de conferência | Acesso aberto |
Jan-2011 | Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes | Temudo, Teresa; Santos, Mónica; Ramos, Elisabete, et al. | Artigo | Acesso aberto |
2008 | The C677T polymorphism in MTHFR is not associated with migraine in Portugal | Ferro, Anabela; Castro, Maria-José; Lemos, Carolina, et al. | Artigo | Acesso aberto |