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Bases neurobiologiques de l’autisme / Caroline KARSENTY
Titre : Bases neurobiologiques de l’autisme Type de document : Texte imprimé et/ou numérique Auteurs : Caroline KARSENTY, Auteur ; Yves CHAIX, Auteur Année de publication : 2013 Importance : p.35-59 Langues : Français (fre) Index. décimale : DEV-B DEV-B - Développement - Généralités Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=222 Bases neurobiologiques de l’autisme [Texte imprimé et/ou numérique] / Caroline KARSENTY, Auteur ; Yves CHAIX, Auteur . - 2013 . - p.35-59.
Langues : Français (fre)
Index. décimale : DEV-B DEV-B - Développement - Généralités Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=222 Exemplaires
Code-barres Cote Support Localisation Section Disponibilité aucun exemplaire Brief Report: Peculiar Evolution of Autistic Behaviors in Two Unrelated Children with Brachidactyly-Mental Retardation Syndrome / Luigi MAZZONE in Journal of Autism and Developmental Disorders, 42-10 (October 2012)
[article]
Titre : Brief Report: Peculiar Evolution of Autistic Behaviors in Two Unrelated Children with Brachidactyly-Mental Retardation Syndrome Type de document : Texte imprimé et/ou numérique Auteurs : Luigi MAZZONE, Auteur ; Lia VASSENA, Auteur ; Liliana RUTA, Auteur ; Diego MUGNO, Auteur ; Ornella GALESI, Auteur ; Marco FICHERA, Auteur Année de publication : 2012 Article en page(s) : p.2202-2207 Langues : Anglais (eng) Mots-clés : Autism 2q37 region BDMR Evolutionary course Index. décimale : PER Périodiques Résumé : Brachidactyly-Mental Retardation (BDMR) Syndrome (MIM 600430) is associated with terminal deletions at chromosome 2q37 and a limited number of studies also reported an association between 2q37 → qter deletion and autism. Herein we describe two cases of autism in unrelated children with BDMR Syndrome, showing physical, cognitive, behavioral, and disease natural history homologies, with a very prominent social impairment in the first 4 years of life. At follow-up evaluations, spanning a 5-years period, both children experienced a progressive reduction of the autistic symptoms, besides retaining compromised cognitive ability. This report supports the hypothesis that genes in the 2q37 region may contribute to the etiology of autism, leading, however, to a peculiar evolution of the disease, with symptoms severity decreasing over time. En ligne : http://dx.doi.org/10.1007/s10803-011-1432-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=180
in Journal of Autism and Developmental Disorders > 42-10 (October 2012) . - p.2202-2207[article] Brief Report: Peculiar Evolution of Autistic Behaviors in Two Unrelated Children with Brachidactyly-Mental Retardation Syndrome [Texte imprimé et/ou numérique] / Luigi MAZZONE, Auteur ; Lia VASSENA, Auteur ; Liliana RUTA, Auteur ; Diego MUGNO, Auteur ; Ornella GALESI, Auteur ; Marco FICHERA, Auteur . - 2012 . - p.2202-2207.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 42-10 (October 2012) . - p.2202-2207
Mots-clés : Autism 2q37 region BDMR Evolutionary course Index. décimale : PER Périodiques Résumé : Brachidactyly-Mental Retardation (BDMR) Syndrome (MIM 600430) is associated with terminal deletions at chromosome 2q37 and a limited number of studies also reported an association between 2q37 → qter deletion and autism. Herein we describe two cases of autism in unrelated children with BDMR Syndrome, showing physical, cognitive, behavioral, and disease natural history homologies, with a very prominent social impairment in the first 4 years of life. At follow-up evaluations, spanning a 5-years period, both children experienced a progressive reduction of the autistic symptoms, besides retaining compromised cognitive ability. This report supports the hypothesis that genes in the 2q37 region may contribute to the etiology of autism, leading, however, to a peculiar evolution of the disease, with symptoms severity decreasing over time. En ligne : http://dx.doi.org/10.1007/s10803-011-1432-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=180 Bringing a developmental perspective to anxiety genetics / Lauren M. MCGRATH in Development and Psychopathology, 24-4 (November 2012)
[article]
Titre : Bringing a developmental perspective to anxiety genetics Type de document : Texte imprimé et/ou numérique Auteurs : Lauren M. MCGRATH, Auteur ; Sydney WEILL, Auteur ; Elise B. ROBINSON, Auteur ; Rebecca MACRAE, Auteur ; Jordan W. SMOLLER, Auteur Année de publication : 2012 Article en page(s) : p.1179-1193 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Despite substantial recent advancements in psychiatric genetic research, progress in identifying the genetic basis of anxiety disorders has been limited. We review the candidate gene and genome-wide literatures in anxiety, which have made limited progress to date. We discuss several reasons for this hindered progress, including small samples sizes, heterogeneity, complicated comorbidity profiles, and blurred lines between normative and pathological anxiety. To address many of these challenges, we suggest a developmental, multivariate framework that can inform and enhance anxiety phenotypes for genetic research. We review the psychiatric and genetic epidemiological evidence that supports such a framework, including the early onset and chronic course of anxiety disorders, shared genetic risk factors among disorders both within and across time, and developmentally dynamic genetic influences. We propose three strategies for developmentally sensitive phenotyping: examination of early temperamental risk factors, use of latent factors to model underlying anxiety liability, and use of developmental trajectories as phenotypes. Expanding the range of phenotypic approaches will be important for advancing studies of the genetic architecture of anxiety disorders. En ligne : http://dx.doi.org/10.1017/S0954579412000636 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=182
in Development and Psychopathology > 24-4 (November 2012) . - p.1179-1193[article] Bringing a developmental perspective to anxiety genetics [Texte imprimé et/ou numérique] / Lauren M. MCGRATH, Auteur ; Sydney WEILL, Auteur ; Elise B. ROBINSON, Auteur ; Rebecca MACRAE, Auteur ; Jordan W. SMOLLER, Auteur . - 2012 . - p.1179-1193.
Langues : Anglais (eng)
in Development and Psychopathology > 24-4 (November 2012) . - p.1179-1193
Index. décimale : PER Périodiques Résumé : Despite substantial recent advancements in psychiatric genetic research, progress in identifying the genetic basis of anxiety disorders has been limited. We review the candidate gene and genome-wide literatures in anxiety, which have made limited progress to date. We discuss several reasons for this hindered progress, including small samples sizes, heterogeneity, complicated comorbidity profiles, and blurred lines between normative and pathological anxiety. To address many of these challenges, we suggest a developmental, multivariate framework that can inform and enhance anxiety phenotypes for genetic research. We review the psychiatric and genetic epidemiological evidence that supports such a framework, including the early onset and chronic course of anxiety disorders, shared genetic risk factors among disorders both within and across time, and developmentally dynamic genetic influences. We propose three strategies for developmentally sensitive phenotyping: examination of early temperamental risk factors, use of latent factors to model underlying anxiety liability, and use of developmental trajectories as phenotypes. Expanding the range of phenotypic approaches will be important for advancing studies of the genetic architecture of anxiety disorders. En ligne : http://dx.doi.org/10.1017/S0954579412000636 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=182 Can Prenatal Factors Cause ASC? / Mina HAH
Titre : Can Prenatal Factors Cause ASC? Type de document : Texte imprimé et/ou numérique Auteurs : Mina HAH, Auteur Année de publication : 2011 Importance : p.102-105 Langues : Anglais (eng) Mots-clés : Facteur prénatal Mercure Vaccination Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=138 Can Prenatal Factors Cause ASC? [Texte imprimé et/ou numérique] / Mina HAH, Auteur . - 2011 . - p.102-105.
Langues : Anglais (eng)
Mots-clés : Facteur prénatal Mercure Vaccination Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=138 Exemplaires
Code-barres Cote Support Localisation Section Disponibilité aucun exemplaire Candidate susceptibility genes for autism / Irina N. BESPALOVA
Titre : Candidate susceptibility genes for autism Type de document : Texte imprimé et/ou numérique Auteurs : Irina N. BESPALOVA, Auteur ; Jennifer REICHERT, Auteur ; Joseph D. BUXBAUM, Auteur Année de publication : 2006 Importance : p.217-232 Langues : Anglais (eng) Index. décimale : SCI-D SCI-D - Neurosciences Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=792 Candidate susceptibility genes for autism [Texte imprimé et/ou numérique] / Irina N. BESPALOVA, Auteur ; Jennifer REICHERT, Auteur ; Joseph D. BUXBAUM, Auteur . - 2006 . - p.217-232.
Langues : Anglais (eng)
Index. décimale : SCI-D SCI-D - Neurosciences Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=792 Exemplaires
Code-barres Cote Support Localisation Section Disponibilité aucun exemplaire Les causes des troubles d’acquisition du langage écrit / Alain CONTENT in Approche Neuropsychologique des Apprentissages chez l'Enfant - A.N.A.E., 116 (Février 2012)
PermalinkCerveau et comportement / Bryan KOLB
PermalinkChildhood adversity and DNA methylation of genes involved in the hypothalamus–pituitary–adrenal axis and immune system: Whole-genome and candidate-gene associations / Johanna BICK in Development and Psychopathology, 24-4 (November 2012)
PermalinkChromosome 15 and autism / Edwin H. Jr COOK
PermalinkChromosome 7 / Beth ROSEN-SHEIDLEY
PermalinkClinique des troubles de l'apprentissage / Christophe-Loïc GERARD
PermalinkCognition sociale et neuropsychologie / Philippe ALLAIN
PermalinkComparison of Siblings of Individuals with Autism and Siblings of Individuals with Other Diagnoses: An Empirical Summary / Nurit YIRMIYA
PermalinkComprehensive Education-Based Mental Health Services for Students Diagnosed on the Autism Spectrum / Raymond W. DUCHARME
PermalinkComprendre et prévenir la déficience intellectuelle / Evelyne PANNETIER
PermalinkConfluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world / Scott I. VRIEZE in Development and Psychopathology, 24-4 (November 2012)
PermalinkControverses sur l'autisme et témoignages / Denys RIBAS
PermalinkA la découverte de l'autisme / Dominique YVON
PermalinkA la découverte de l'autisme / Dominique YVON
PermalinkLa déficience intellectuelle / Jean-François MARTIN
PermalinkLa déficience intellectuelle face aux progrès des neurosciences / Roland BROCA
PermalinkDéficiences intellectuelles et intégration sociale / Michèle CARLIER
PermalinkDéficit de l'attention-hyperactivité chez l'adulte / Nader PERROUD
PermalinkDefining behavioural phenotypes: exploring phenotype/genotype interrelationships / Gregory O'BRIEN
PermalinkDevelopmental genetics and psychopathology: Some new feathers for a fine old hat / Wendy JOHNSON in Development and Psychopathology, 24-4 (November 2012)
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