Percorrer por assunto Neurodevelopment

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DataTítuloAutor(es)TipoAcesso
2011Abnormal processing of emotional prosody in Williams syndrome: an event-related potentials studyPinheiro, Ana P.; Galdo-Álvarez, Santiago; Rauber, Andréia Schurt, et al.ArtigoAcesso aberto
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
Ago-2011Autobiographical narratives in Williams Syndrome: structural, process and content dimensionsGonçalves, Óscar F.; Pinheiro, Ana P.; Sampaio, Adriana, et al.ArtigoAcesso aberto
2012Cognitive functioning in children and adults with Smith-Magenis syndromeOsório, Ana Alexandra Caldas; Cruz, Raquel; Sampaio, Adriana, et al.ArtigoAcesso aberto
2009Cognitive functioning in Williams syndrome: a study in Portuguese and Spanish patientsSampaio, Adriana; Férnandez, Montse; Henriques, Margarida Rangel, et al.ArtigoAcesso aberto
Ago-2012Do genes and environment meet to regulate cerebrospinal fluid dynamics? Relevance for schizophreniaPalha, Joana Almeida; Santos, Nadine Correia; Marques, Fernanda Cristina Gomes de Sousa, et al.ArtigoAcesso aberto
2010Electrophysiological correlates of semantic processing in Williams syndromePinheiro, Ana P.; Galdo-Álvarez, Santiago; Sampaio, Adriana, et al.ArtigoAcesso restrito UMinho
Abr-2007Evidence for abnormal early development in a mouse model of Rett syndromeSantos, Mónica; Silva-Fernandes, Anabela; Oliveira, P., et al.ArtigoAcesso restrito UMinho
6-Nov-2006Febrile convulsions in developing rats induce a hyperanxious phenotype later in lifeMesquita, Ana Raquel Marcelino; Tavares, H. B.; Silva, Rui Jorge, et al.ArtigoAcesso restrito UMinho
5-Jul-2019Genomic imbalances defining novel intellectual disability associated lociLopes, Fátima Daniela Teixeira; Torres, Fátima; Soares, Gabriela, et al.ArtigoAcesso aberto
Jun-2009Glucocorticoids and neuro- and behavioural developmentMesquita, Ana Raquel Marcelino; Wegerich, Yvonne; Patchev, Alexandre V., et al.ArtigoAcesso restrito UMinho
14-Dez-2022HCN channelopathy as a key mechanism for auditory hypersensitivity in a shank3 mouse model of ASDCastro, Ana Carolina PintoDissertação de mestrado Acesso restrito autor
1-Mai-2006Induction of a hyperanxious state by antenatal dexamethasone: a case for less detrimental natural corticosteroidsOliveira, Mário Jorge Alves; Bessa, João M.; Mesquita, Ana, et al.ArtigoAcesso restrito UMinho
2020Infants' cortical processing of biological motion configuration - A fNIRS studyLisboa, Isabel C; Queirós, Sandra; Miguel, Helga, et al.ArtigoAcesso restrito UMinho
Abr-2008Memory abilities in Williams syndrome: dissociation or developmental delay hypothesis?Sampaio, Adriana; Sousa, Nuno; Férnandez, Montse, et al.ArtigoAcesso aberto
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
Mai-2013Morphometry of corpus callosum in Williams syndrome: shape as an index of neural developmentSampaio, Adriana; Bouix, Sylvain; Sousa, Nuno, et al.ArtigoAcesso restrito UMinho
2011MRI amygdala volume in Williams syndromeCapitão, Liliana; Sampaio, Adriana; Sampaio, Cassandra, et al.ArtigoAcesso aberto
6-Jun-2008MRI assessment of superior temporal gyrus in Williams syndromeSampaio, Adriana; Sousa, Nuno; Férnandez, Montse, et al.ArtigoAcesso aberto
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