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Auteur Miguel Angel DE LEON MIRANDA |
Documents disponibles écrits par cet auteur (1)
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An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome / Carlos Alberto SERRANO-JUAREZ in Journal of Autism and Developmental Disorders, 51-5 (May 2021)
[article]
Titre : An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome Type de document : Texte imprimé et/ou numérique Auteurs : Carlos Alberto SERRANO-JUAREZ, Auteur ; Belén PRIETO-CORONA, Auteur ; Mario RODRIGUEZ-CAMACHO, Auteur ; Carlos Alberto VENEGAS-VEGA, Auteur ; Ma Guillermina YAÑEZ-TELLEZ, Auteur ; Juan SILVA-PEREYRA, Auteur ; Hermelinda SALGADO-CEBALLOS, Auteur ; Natalia ARIAS-TREJO, Auteur ; Miguel Angel DE LEON MIRANDA, Auteur Article en page(s) : p.1695-1704 Langues : Anglais (eng) Mots-clés : GTF2I family Gtf2ird2 Genotypes Social cognition Social phenotype Williams syndrome Index. décimale : PER Périodiques Résumé : An explanation for the social dysfunction observed in Williams syndrome may be deficits in social cognition. This study explored aspects of social cognition in children with Williams syndrome with different genotypes. The 12 participants included one with a 1.1 Mb deletion that retained the GTF2IRD1, GTF2I, and GTF2IRD2 genes, seven with a 1.5 Mb deletion that preserved the GTF2IRD2 gene, and four with a 1.8 Mb deletion with loss of all three genes. The participant retaining all three genes was found to have better performance on social judgment and first-order theory of mind tasks than the group with loss of all three genes. These results may reflect the influence of the GTF2I gene family on social cognition in Williams syndrome. En ligne : http://dx.doi.org/10.1007/s10803-020-04656-4 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=445
in Journal of Autism and Developmental Disorders > 51-5 (May 2021) . - p.1695-1704[article] An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome [Texte imprimé et/ou numérique] / Carlos Alberto SERRANO-JUAREZ, Auteur ; Belén PRIETO-CORONA, Auteur ; Mario RODRIGUEZ-CAMACHO, Auteur ; Carlos Alberto VENEGAS-VEGA, Auteur ; Ma Guillermina YAÑEZ-TELLEZ, Auteur ; Juan SILVA-PEREYRA, Auteur ; Hermelinda SALGADO-CEBALLOS, Auteur ; Natalia ARIAS-TREJO, Auteur ; Miguel Angel DE LEON MIRANDA, Auteur . - p.1695-1704.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 51-5 (May 2021) . - p.1695-1704
Mots-clés : GTF2I family Gtf2ird2 Genotypes Social cognition Social phenotype Williams syndrome Index. décimale : PER Périodiques Résumé : An explanation for the social dysfunction observed in Williams syndrome may be deficits in social cognition. This study explored aspects of social cognition in children with Williams syndrome with different genotypes. The 12 participants included one with a 1.1 Mb deletion that retained the GTF2IRD1, GTF2I, and GTF2IRD2 genes, seven with a 1.5 Mb deletion that preserved the GTF2IRD2 gene, and four with a 1.8 Mb deletion with loss of all three genes. The participant retaining all three genes was found to have better performance on social judgment and first-order theory of mind tasks than the group with loss of all three genes. These results may reflect the influence of the GTF2I gene family on social cognition in Williams syndrome. En ligne : http://dx.doi.org/10.1007/s10803-020-04656-4 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=445