| Data | Título | Autor(es) | Tipo | Acesso |
| Out-2009 | Analysis of microsatellite instability in medulloblastoma | Pereira, Marta Sofia Carvalho Ribeiro Viana; Almeida, Inês; Sousa, Sónia, et al. | Artigo | Acesso aberto |
| Jan-2009 | Evaluation of CSF neurotransmitters and folate in 25 patients with Rett disorder and effects of treatment | Temudo, T.; Rios, M.; Prior, C., et al. | Artigo | Acesso aberto |
| 2017 | Functional characterization of a 28-Kilobase Catabolic Island from Pseudomonas sp. Strain M1 involved in biotransformation of β-Myrcene and related plant-derived volatiles | Castro, Pedro Miguel Soares; Silva, Pedro Montenegro; Heipieper, Hermann J., et al. | Artigo | Acesso aberto |
| 2019 | Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3 | Hosie, Suzanne; Ellis, Melina; Swaminathan, Mathusi, 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 |
| Fev-2008 | Molecular alterations of KIT and PDGFRA in GISTs: evaluation of a Portuguese series | Gomes, A. L.; Gouveia, A.; Capelinha, A. F., et al. | Artigo | Acesso aberto |
| Out-2010 | Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis | Pinho, Teresa; Silva-Fernandes, Anabela; Bousbaa, Hassan, et al. | Artigo | Acesso aberto |
| 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 |
| Abr-2007 | Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations | Temudo, T.; Oliveira, P.; Santos, M., et al. | Artigo | Acesso restrito UMinho |
