Data | Título | Autor(es) | Tipo | Acesso |
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 |
14-Out-2020 | Artificial intelligence within the interplay between natural and artificial computation: Advances in data science, trends and applications | Górriz, Juan M.; Ramírez, Javier; Ortíz, Andrés, et al. | Artigo | Acesso restrito UMinho |
2-Nov-2022 | Autism spectrum as an etiologic systemic disorder: a protocol for an umbrella review | Lopes, Lara Teixeira; Rodrigues, Jorge Magalhães; Baccarin, Celeste, et al. | Artigo | Acesso aberto |
17-Jun-2022 | Autismo e desenvolvimento de carreira: eficácia e impacto de uma intervenção com pais | Carvalho, Marisa Andrea Magalhães Ferreira de | Dissertação de mestrado | Acesso aberto |
2018 | Development of activities for human-robot interaction: preliminary results | Costa, Pedro Gonçalves da; Freitas, Helder Filipe Costa; Soares, Filomena, et al. | Artigo em ata de conferência | Acesso restrito autor |
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 |
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 |
13-Out-2010 | Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome | Santos, M.; Summavielle, T.; Teixeira-Castro, A., 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 |
27-Abr-2023 | O processo de transição da criança com Transtorno do Espectro do Autismo para o ensino fundamental: preocupações de mães em Brasília | Araújo, Aline Oliveira de | Dissertação de mestrado | 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 |
2021 | Social camouflaging in females with autism spectrum disorder: A systematic review | Tubío-Fungueiriño, María; Cruz, Sara; Sampaio, Adriana, et al. | Artigo | Acesso restrito UMinho |
Jul-2023 | STEAM and inclusive education: hands-on science experiments using static electricity | Costa, Manuel F. M.; Marques, M. | Capítulo de livro | Acesso aberto |
1-Jan-2017 | A task recommendation system for children and youth with autism spectrum disorder | Costa, Margarida; Costa, Angelo; Julián, Vicente, et al. | Artigo em ata de conferência | Acesso aberto |
2019 | The child with Autism Spectrum Disorder: the perceptions of siblings | Costa, Teresa Macedo; Pereira, Ana Paula da Silva | Artigo | Acesso aberto |
Mar-2013 | Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disorders | Bessa, C.; Maciel, P.; Rodrigues, Ana João | Artigo | Acesso aberto |