Browsing by subject Intellectual disability

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Showing results 1 to 12 of 12.
Issue DateTitleAuthor(s)TypeAccess
2023Barriers to volunteering in the field of intellectual disability: a cluster analysisCruz, Soraia; Ferreira, Marisa Roriz; Borges, Ana, et al.ArticleOpen access
3-Jan-2021Clinical and molecular findings in a Turkish family with an ultra-rare condition, ELP2-related neurodevelopmental disorderDogan, Mustafa; Terali, Kerem; Eroz, Recep, et al.ArticleRestricted access (UMinho)
2016Competências profissionais num centro de atividades ocupacionaisOliveira, Susana Carvalheira Corte-RealMaster thesis Restricted access (UMinho)
2011Estudo genético do atraso mental em Portugal : desenvolvimento de métodos de deteção da dosagem alterada de genes com vista ao diagnóstico molecularSousa, Susana de Fátima Mendes eMaster thesis Restricted access (UMinho)
9-Feb-2016Identification of novel genetic causes of Rett syndrome-like phenotypesLopes, Fátima Daniela Teixeira; Barbosa, Mafalda Fernanda Cabral Santos; Soares, Gabriela, et al.ArticleOpen access
21-Sep-2017A novel microduplication of ARID1B: Clinical, genetic, and proteomic findingsSeabra, Catarina M.; Szoko, Nicholas; Erdin, Serkan, et al.ArticleOpen access
2015Performing universal tasks on the Web: Interaction with digital content by people with intellectual disabilitiesRocha, Tânia; Bessa, Maximino; Magalhães, Luís Gonzaga Mendes, et al.Conference paperRestricted access (UMinho)
22-Jan-2019Perspetivas sobre a transição para a vida pós-escolar de alunos com dificuldade intelectualFerreira, Maria do Rosário de AraújoDoctoral thesisRestricted access (UMinho)
2018“Sem Etiquetas”: uma página Facebook para a inclusão digital de adultos com incapacidade intelectualFernandes, Diana Andreia EstevesMaster thesis Open access
2017Usability evaluation of navigation tasks by people with intellectual disabilities: a Google and SAPO comparative study regarding different interaction modalitiesRocha, Tania; Carvalho, Diana; Bessa, Maximino, et al.ArticleRestricted access (UMinho)
Mar-2013Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disordersBessa, C.; Maciel, P.; Rodrigues, Ana JoãoArticleOpen access
10-Nov-2015Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 geneVieira, José Pedro; Lopes, Fátima Daniela Teixeira; Fernandes, Anabela Silva, et al.ArticleOpen access