Percorrer por assunto Autism

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Mostrar 1-17 de um total de 17 resultados.
DataTítuloAutor(es)TipoAcesso
2008Analysis 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 retardationSantos, Mónica; Yan, Jin; Temudo, Teresa, et al.ArtigoAcesso restrito UMinho
14-Out-2020Artificial intelligence within the interplay between natural and artificial computation: Advances in data science, trends and applicationsGórriz, Juan M.; Ramírez, Javier; Ortíz, Andrés, et al.ArtigoAcesso restrito UMinho
2-Nov-2022Autism spectrum as an etiologic systemic disorder: a protocol for an umbrella reviewLopes, Lara Teixeira; Rodrigues, Jorge Magalhães; Baccarin, Celeste, et al.ArtigoAcesso aberto
17-Jun-2022Autismo e desenvolvimento de carreira: eficácia e impacto de uma intervenção com paisCarvalho, Marisa Andrea Magalhães Ferreira deDissertação de mestrado Acesso aberto
2018Development of activities for human-robot interaction: preliminary resultsCosta, Pedro Gonçalves da; Freitas, Helder Filipe Costa; Soares, Filomena, et al.Artigo em ata de conferênciaAcesso restrito autor
Abr-2007Evidence for abnormal early development in a mouse model of Rett syndromeSantos, Mónica; Silva-Fernandes, Anabela; Oliveira, P., et al.ArtigoAcesso restrito UMinho
2019Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3Hosie, Suzanne; Ellis, Melina; Swaminathan, Mathusi, 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
13-Out-2010Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndromeSantos, M.; Summavielle, T.; Teixeira-Castro, A., 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
27-Abr-2023O processo de transição da criança com Transtorno do Espectro do Autismo para o ensino fundamental: preocupações de mães em BrasíliaAraújo, Aline Oliveira deDissertação de mestrado Acesso aberto
Jan-2011Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypesTemudo, Teresa; Santos, Mónica; Ramos, Elisabete, et al.ArtigoAcesso aberto
2021Social camouflaging in females with autism spectrum disorder: A systematic reviewTubío-Fungueiriño, María; Cruz, Sara; Sampaio, Adriana, et al.ArtigoAcesso restrito UMinho
Jul-2023STEAM and inclusive education: hands-on science experiments using static electricityCosta, Manuel F. M.; Marques, M.Capítulo de livroAcesso aberto
1-Jan-2017A task recommendation system for children and youth with autism spectrum disorderCosta, Margarida; Costa, Angelo; Julián, Vicente, et al.Artigo em ata de conferênciaAcesso aberto
2019The child with Autism Spectrum Disorder: the perceptions of siblingsCosta, Teresa Macedo; Pereira, Ana Paula da SilvaArtigoAcesso aberto
Mar-2013Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disordersBessa, C.; Maciel, P.; Rodrigues, Ana JoãoArtigoAcesso aberto