Centre d'Information et de documentation du CRA Rhône-Alpes
CRA
Informations pratiques
-
Adresse
Centre d'information et de documentation
du CRA Rhône-Alpes
Centre Hospitalier le Vinatier
bât 211
95, Bd Pinel
69678 Bron CedexHoraires
Lundi au Vendredi
9h00-12h00 13h30-16h00Contact
Tél: +33(0)4 37 91 54 65
Mail
Fax: +33(0)4 37 91 54 37
-
Détail de l'auteur
Auteur Susan HARRIS |
Documents disponibles écrits par cet auteur (1)
Faire une suggestion Affiner la recherche
Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype? / Kathleen ANGKUSTSIRI in Journal of Autism and Developmental Disorders, 44-4 (April 2014)
[article]
Titre : Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype? Type de document : Texte imprimé et/ou numérique Auteurs : Kathleen ANGKUSTSIRI, Auteur ; Beth GOODLIN-JONES, Auteur ; Lesley DEPREY, Auteur ; Khyati BRAHMBHATT, Auteur ; Susan HARRIS, Auteur ; Tony J. SIMON, Auteur Année de publication : 2014 Article en page(s) : p.739-746 Langues : Anglais (eng) Mots-clés : Autism ASD 22q11.2 deletion syndrome Velocardiofacial syndrome Index. décimale : PER Périodiques Résumé : High prevalence of autism spectrum disorders (ASD) has been reported in 22q11.2DS, although this has been based solely on parent report measures. This study describes the presence of ASD using a procedure more similar to that used in clinical practice by incorporating history (Social Communication Questionnaire) AND a standardized observation measure (Autism Diagnostic Observation Schedule) and suggests that ASD is not as common as previously reported in 22q11.2DS. Differences in methodology, along with comorbid conditions such as anxiety, likely contribute to false elevations in ASD prevalence and information from multiple sources should be included in the evaluation of ASD. En ligne : http://dx.doi.org/10.1007/s10803-013-1920-x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=228
in Journal of Autism and Developmental Disorders > 44-4 (April 2014) . - p.739-746[article] Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype? [Texte imprimé et/ou numérique] / Kathleen ANGKUSTSIRI, Auteur ; Beth GOODLIN-JONES, Auteur ; Lesley DEPREY, Auteur ; Khyati BRAHMBHATT, Auteur ; Susan HARRIS, Auteur ; Tony J. SIMON, Auteur . - 2014 . - p.739-746.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 44-4 (April 2014) . - p.739-746
Mots-clés : Autism ASD 22q11.2 deletion syndrome Velocardiofacial syndrome Index. décimale : PER Périodiques Résumé : High prevalence of autism spectrum disorders (ASD) has been reported in 22q11.2DS, although this has been based solely on parent report measures. This study describes the presence of ASD using a procedure more similar to that used in clinical practice by incorporating history (Social Communication Questionnaire) AND a standardized observation measure (Autism Diagnostic Observation Schedule) and suggests that ASD is not as common as previously reported in 22q11.2DS. Differences in methodology, along with comorbid conditions such as anxiety, likely contribute to false elevations in ASD prevalence and information from multiple sources should be included in the evaluation of ASD. En ligne : http://dx.doi.org/10.1007/s10803-013-1920-x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=228