| Issue Date | Title | Author(s) | Type | Access |
| Nov-2007 | Abnormal movements in Rett syndrome are present before the regression period: a case study | Temudo, Teresa; Maciel, P.; Sequeiros, Jorge | Article | Restricted access (UMinho) |
| 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. | Article | Restricted access (UMinho) |
| 15-Mar-2008 | Atypical stereotypies and vocal tics in Rett syndrome: an illustrative case | Temudo, Teresa; Freitas, Paula; Sequeiros, Jorge, et al. | Letter to the editor | Restricted access (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. | Article | Open access |
| 5-Jul-2019 | Genomic imbalances defining novel intellectual disability associated loci | Lopes, Fátima Daniela Teixeira; Torres, Fátima; Soares, Gabriela, et al. | Article | Open access |
| 9-Feb-2016 | Identification of novel genetic causes of Rett syndrome-like phenotypes | Lopes, Fátima Daniela Teixeira; Barbosa, Mafalda Fernanda Cabral Santos; Soares, Gabriela, et al. | Article | Open access |
| Jun-2007 | MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients | Coutinho, Ana M.; Oliveira, Guiomar; Katz, Cécile, et al. | Article | Restricted access (UMinho) |
| 30-Jul-2008 | Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type | Temudo, Teresa; Ramos, Elisabete; Dias, Karin, et al. | Article | Restricted access (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. | Article | Open access |
| Jan-2011 | Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes | Temudo, Teresa; Santos, Mónica; Ramos, Elisabete, et al. | Article | Open access |
| 10-Nov-2015 | Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene | Vieira, José Pedro; Lopes, Fátima Daniela Teixeira; Fernandes, Anabela Silva, et al. | Article | Open access |
