Williams syndrome (WS) is a rare genetic disease involving an intellectual developmental disorder (ID). Regarding the neuropsychological level, a consensus around a dissociation profile between relatively preserved oral language and other impaired cognitive abilities is reported in the literature. Despite these specificities, few studies have investigated the learning aspects in this population, and more specifically the reading area. Three explanatory hypotheses are shared by the few reported results regarding the reading acquisition difficulties: intellectual efficiency, metaphonological abilities and, more recently, visuospatial processing. In line with this work, our research attempts, for the first time in France, to better understand ...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Williams Syndrome (WS) is a genetic neurodevelopmental disorder caused by a submicroscopic deletion...
ABSTRACT Williams syndrome is a neurodevelopmental disorder with different manifestations caused by ...
Williams syndrome (WS) is a rare genetic disease involving an intellectual developmental disorder (I...
Le syndrome de Williams (SW) est une maladie génétique rare admettant un trouble du développement in...
International audiencePurpose Multiple factors impact reading acquisition in individuals with readin...
International audienceThe research on reading in the context of Williams Syndrome (WS) suggests diff...
This research aims to study the development of language, theory of mind and emotion recognition in W...
Summary : Visuo-constructive impairments in Williams syndrome. Williams syndrome (WS) is a genetical...
Cette recherche a pour objectif d'étudier le développement des capacités en langage, en théorie de l...
Important claims have been made regarding the contrasting profiles of linguistic and cognitive perfo...
Williams syndrome is a rare genetic disorder in which, it is claimed, language abilities are relativ...
The objective of this study was to investigate the psycholinguistic abilities of children with Will...
The aims of this study were twofold: (1) to explore theoretical links between the neuropsychological...
A Síndrome de Williams-Beuren (Williams, 1961, Beuren, 1962) possui um perfil específico caracteriza...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Williams Syndrome (WS) is a genetic neurodevelopmental disorder caused by a submicroscopic deletion...
ABSTRACT Williams syndrome is a neurodevelopmental disorder with different manifestations caused by ...
Williams syndrome (WS) is a rare genetic disease involving an intellectual developmental disorder (I...
Le syndrome de Williams (SW) est une maladie génétique rare admettant un trouble du développement in...
International audiencePurpose Multiple factors impact reading acquisition in individuals with readin...
International audienceThe research on reading in the context of Williams Syndrome (WS) suggests diff...
This research aims to study the development of language, theory of mind and emotion recognition in W...
Summary : Visuo-constructive impairments in Williams syndrome. Williams syndrome (WS) is a genetical...
Cette recherche a pour objectif d'étudier le développement des capacités en langage, en théorie de l...
Important claims have been made regarding the contrasting profiles of linguistic and cognitive perfo...
Williams syndrome is a rare genetic disorder in which, it is claimed, language abilities are relativ...
The objective of this study was to investigate the psycholinguistic abilities of children with Will...
The aims of this study were twofold: (1) to explore theoretical links between the neuropsychological...
A Síndrome de Williams-Beuren (Williams, 1961, Beuren, 1962) possui um perfil específico caracteriza...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Williams Syndrome (WS) is a genetic neurodevelopmental disorder caused by a submicroscopic deletion...
ABSTRACT Williams syndrome is a neurodevelopmental disorder with different manifestations caused by ...