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Genomic structural variation in psychiatric disorders / James J. H. RUCKER in Development and Psychopathology, 24-4 (November 2012)
[article]
Titre : Genomic structural variation in psychiatric disorders Type de document : Texte imprimé et/ou numérique Auteurs : James J. H. RUCKER, Auteur ; Peter MCGUFFIN, Auteur Année de publication : 2012 Article en page(s) : p.1335-1344 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Copy number variants (CNVs) are submicroscopic deletions and duplications of genomic material that were previously thought to be rare phenomena. They have now been robustly associated with a variety of disorders such as autism, schizophrenia, and attention-deficit/hyperactivity disorder through an emerging research base in affective disorders. A complex picture is emerging of a polygenic, heterogeneous model of disease, with CNVs conferring broad susceptibility to a variety of neurodevelopmental disorders, rather than specific disorders per se. Although the insights gleaned thus far only represent a small piece of a much larger puzzle, progress has been rapid and new technologies promise even more insights into these hitherto opaque brain disorders. We will discuss CNVs, the current state of evidence for their role in the pathogenesis of classical psychiatric disorders, and the application of such knowledge in clinical settings. En ligne : http://dx.doi.org/10.1017/S0954579412000740 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.1335-1344[article] Genomic structural variation in psychiatric disorders [Texte imprimé et/ou numérique] / James J. H. RUCKER, Auteur ; Peter MCGUFFIN, Auteur . - 2012 . - p.1335-1344.
Langues : Anglais (eng)
in Development and Psychopathology > 24-4 (November 2012) . - p.1335-1344
Index. décimale : PER Périodiques Résumé : Copy number variants (CNVs) are submicroscopic deletions and duplications of genomic material that were previously thought to be rare phenomena. They have now been robustly associated with a variety of disorders such as autism, schizophrenia, and attention-deficit/hyperactivity disorder through an emerging research base in affective disorders. A complex picture is emerging of a polygenic, heterogeneous model of disease, with CNVs conferring broad susceptibility to a variety of neurodevelopmental disorders, rather than specific disorders per se. Although the insights gleaned thus far only represent a small piece of a much larger puzzle, progress has been rapid and new technologies promise even more insights into these hitherto opaque brain disorders. We will discuss CNVs, the current state of evidence for their role in the pathogenesis of classical psychiatric disorders, and the application of such knowledge in clinical settings. En ligne : http://dx.doi.org/10.1017/S0954579412000740 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=182 Gut and Psychology Syndrome / Natasha CAMPBELL-MCBRIDE
Titre : Gut and Psychology Syndrome : Natural Treatment for Autism,ADD/ADHD,Dyslexia,Dyspraxia,Depression,Schizophrenia Type de document : Texte imprimé et/ou numérique Auteurs : Natasha CAMPBELL-MCBRIDE, Auteur Editeur : Cambridge [Angleterre] : Medinform Publishing Année de publication : 2004 Importance : 266 p. Présentation : ill. Format : 15cm x 21cm x 1,7cm ISBN/ISSN/EAN : 978-0-9548520-0-9 Note générale : Bibliogr., Index Langues : Anglais (eng) Index. décimale : VIE-B VIE-B - Vie Quotidienne - Alimentation Résumé : Dr. Natasha Campbell-McBride set up The Cambridge Nutrition Clinic in 1998. As a parent of a child diagnosed with learning disabilities, she was acutely aware of the difficulties facing other parents like her, and she has devoted much of her time to helping these families. She realised that nutrition played a critical role in helping children and adults to overcome their disabilities, and has pioneered the use of probiotics in this field.
Her willingness to share her knowledge has resulted in her contributing to many publications, as well as presenting at numerous seminars and conferences on the subjects of learning disabilities and digestive disorders. Her book "Gut and Psychology Syndrome" captures her experience and knowledge, incorporating her most recent work.
She believes that the link between learning disabilities, the food and drink that we take, and the condition of our digestive system is absolute, and the results of her work have supported her position on this subject. In her clinic, parents discuss all aspects of their child's condition, confident in the knowledge that they are not only talking to a professional but to a parent who has lived their experience. Her deep understanding of the challenges they face, puts her advice in a class of it's own.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=759 Gut and Psychology Syndrome : Natural Treatment for Autism,ADD/ADHD,Dyslexia,Dyspraxia,Depression,Schizophrenia [Texte imprimé et/ou numérique] / Natasha CAMPBELL-MCBRIDE, Auteur . - Cambridge [Angleterre] : Medinform Publishing, 2004 . - 266 p. : ill. ; 15cm x 21cm x 1,7cm.
ISBN : 978-0-9548520-0-9
Bibliogr., Index
Langues : Anglais (eng)
Index. décimale : VIE-B VIE-B - Vie Quotidienne - Alimentation Résumé : Dr. Natasha Campbell-McBride set up The Cambridge Nutrition Clinic in 1998. As a parent of a child diagnosed with learning disabilities, she was acutely aware of the difficulties facing other parents like her, and she has devoted much of her time to helping these families. She realised that nutrition played a critical role in helping children and adults to overcome their disabilities, and has pioneered the use of probiotics in this field.
Her willingness to share her knowledge has resulted in her contributing to many publications, as well as presenting at numerous seminars and conferences on the subjects of learning disabilities and digestive disorders. Her book "Gut and Psychology Syndrome" captures her experience and knowledge, incorporating her most recent work.
She believes that the link between learning disabilities, the food and drink that we take, and the condition of our digestive system is absolute, and the results of her work have supported her position on this subject. In her clinic, parents discuss all aspects of their child's condition, confident in the knowledge that they are not only talking to a professional but to a parent who has lived their experience. Her deep understanding of the challenges they face, puts her advice in a class of it's own.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=759 Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité DOC0000800 VIE-B CAM Livre Centre d'Information et de Documentation du CRA Rhône-Alpes VIE -Vie quotidienne Disponible Handbook of Interdisciplinary Treatments for Autism Spectrum Disorder / Robert D. RIESKE
Titre : Handbook of Interdisciplinary Treatments for Autism Spectrum Disorder Type de document : Texte imprimé et/ou numérique Auteurs : Robert D. RIESKE, Directeur de publication Editeur : Berlin [Allemagne] : Springer Année de publication : 2019 Collection : Autism and Child Psychopathology Series, ISSN 2192-922X Importance : 479 p. Format : 18cm x 25cm x 3,5cm ISBN/ISSN/EAN : 978-3-030-13026-8 Note générale : Bibliogr., Index Langues : Anglais (eng) Mots-clés : Gastroenterologie Index. décimale : AUT-F AUT-F - L'Autisme - Soins Résumé : This handbook examines the medical and therapeutic needs of individuals with autism spectrum disorder (ASD) and the effectiveness of treatments that are delivered through interdisciplinary teams. It analyzes the impact of interdisciplinary teams on assessment, diagnosis, treatment planning, and implementation and explores how evidence-based treatments can be developed and implemented. Chapters describe the wide-ranging effects of ASD and the challenges individuals and their family members face when seeking treatment. In addition, chapters provide an overview of the comorbidities and related disorders that often accompany ASD, including neurodevelopmental disorders, medical and behavioral problems, and psychopathology. The handbook also discusses the critical importance of caregivers in the treatment team as experts in their child’s strengths, problem areas, and functioning.
Topics featured in this handbook include:
Legal considerations in interdisciplinary treatments.
Ethical considerations in the development and implementation of interdisciplinary teams.
Evidence-based interdisciplinary treatment and evaluation considerations.
The role of primary care physicians and subspecialty pediatricians within interdisciplinary teams.
The impact of school psychologists related to assessment and intervention development.
Vocational interventions that promote independence in individuals with ASD.
The Handbook of Interdisciplinary Treatments for Autism Spectrum Disorder is a must-have resource for researchers, clinicians and professionals, and graduate students across such interrelated disciplines as clinical child, school, and developmental psychology, child and adolescent psychiatry, social work, rehabilitation medicine/therapy, pediatrics, and special education. [Résumé d'Auteur/Editeur]Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=418 Handbook of Interdisciplinary Treatments for Autism Spectrum Disorder [Texte imprimé et/ou numérique] / Robert D. RIESKE, Directeur de publication . - Berlin [Allemagne] : Springer, 2019 . - 479 p. ; 18cm x 25cm x 3,5cm. - (Autism and Child Psychopathology Series, ISSN 2192-922X) .
ISBN : 978-3-030-13026-8
Bibliogr., Index
Langues : Anglais (eng)
Mots-clés : Gastroenterologie Index. décimale : AUT-F AUT-F - L'Autisme - Soins Résumé : This handbook examines the medical and therapeutic needs of individuals with autism spectrum disorder (ASD) and the effectiveness of treatments that are delivered through interdisciplinary teams. It analyzes the impact of interdisciplinary teams on assessment, diagnosis, treatment planning, and implementation and explores how evidence-based treatments can be developed and implemented. Chapters describe the wide-ranging effects of ASD and the challenges individuals and their family members face when seeking treatment. In addition, chapters provide an overview of the comorbidities and related disorders that often accompany ASD, including neurodevelopmental disorders, medical and behavioral problems, and psychopathology. The handbook also discusses the critical importance of caregivers in the treatment team as experts in their child’s strengths, problem areas, and functioning.
Topics featured in this handbook include:
Legal considerations in interdisciplinary treatments.
Ethical considerations in the development and implementation of interdisciplinary teams.
Evidence-based interdisciplinary treatment and evaluation considerations.
The role of primary care physicians and subspecialty pediatricians within interdisciplinary teams.
The impact of school psychologists related to assessment and intervention development.
Vocational interventions that promote independence in individuals with ASD.
The Handbook of Interdisciplinary Treatments for Autism Spectrum Disorder is a must-have resource for researchers, clinicians and professionals, and graduate students across such interrelated disciplines as clinical child, school, and developmental psychology, child and adolescent psychiatry, social work, rehabilitation medicine/therapy, pediatrics, and special education. [Résumé d'Auteur/Editeur]Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=418 Contenu
- Interdisciplinary Teams and Autism Spectrum Disorder / Michelle S. LEMAY
- Ethical Considerations in Interdisciplinary Treatments / David J. COX
- Evidenced-Based Practices / Costanza COLOMBI
- Comorbidity and the Need for Interdisciplinary Treatments / Johnny L. MATSON
- Legal Considerations in Interdisciplinary Treatments / Maria C. MCGINLEY
- Interdisciplinary Diagnostic Evaluations / Brett A. ENNEKING
- Applied Behavior Analysis and Related Treatments / Heidi R. FISHER
- Interdisciplinary Treatment for Pediatric Feeding Disorders / Cy NADLER
- Interdisciplinary Treatment for Pediatric Elimination Disorders / Christina LOW KAPALU
- Development of the Interdisciplinary Treatment Team / Christine M. RACHES
- Psychology / Lindsey W. WILLIAMS
- Primary Care Physicians/Subspecialty Pediatricians / Julie N. YOUSSEF
- Speech-Language Pathology / Stacy S. MANWARING
- Occupational and Physical Therapy / Bryan M. GEE
- Dietetics/Nutrition / Allisha M. WEEDEN
- Gastroenterology / Sylvia Y. OFEI
- Neurologic Music Therapy / Michael H. THAUT
- Oral Health / Leciel K. BONO
- School Psychology and Education Professionals / Aaron J. FISCHER
- Vocational Interventions / Paul WEHMAN
20 notices affichées sur 24, voir les 4 autresExemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité DOC0005338 AUT-F RIE Livre Centre d'Information et de Documentation du CRA Rhône-Alpes AUT - L'Autisme Disponible Handicap et fratrie / SESSAD LES MARMOTS
Titre : Handicap et fratrie : Actes de la table ronde du 1er octobre 1992 organisée par le SESSAD les Marmots Type de document : Texte imprimé et/ou numérique Auteurs : SESSAD LES MARMOTS, Auteur Editeur : Besançon [France] : Sessad les Marmots Année de publication : 1992 Importance : 51 p. Format : 21cm x 29,7cm x 1cm Note générale : Bibliogr. Langues : Français (fre) Mots-clés : Gemellité Index. décimale : VIE-E VIE-E - Vie Quotidienne - Fratrie Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442 Handicap et fratrie : Actes de la table ronde du 1er octobre 1992 organisée par le SESSAD les Marmots [Texte imprimé et/ou numérique] / SESSAD LES MARMOTS, Auteur . - Besançon [France] : Sessad les Marmots, 1992 . - 51 p. ; 21cm x 29,7cm x 1cm.
Bibliogr.
Langues : Français (fre)
Mots-clés : Gemellité Index. décimale : VIE-E VIE-E - Vie Quotidienne - Fratrie Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442 Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité DOC0005988 VIE-E MAR Livre Centre d'Information et de Documentation du CRA Rhône-Alpes VIE -Vie quotidienne Disponible Haploinsufficiency of CMIP in a Girl With Autism Spectrum Disorder and Developmental Delay due to a De Novo Deletion on Chromosome 16q23.2 / Nathalie VAN DER AA in Autism Research, 5-4 (August 2012)
[article]
Titre : Haploinsufficiency of CMIP in a Girl With Autism Spectrum Disorder and Developmental Delay due to a De Novo Deletion on Chromosome 16q23.2 Type de document : Texte imprimé et/ou numérique Auteurs : Nathalie VAN DER AA, Auteur ; Geert VANDEWEYER, Auteur ; Edwin REYNIERS, Auteur ; Sandra KENIS, Auteur ; Lina DOM, Auteur ; Geert MORTIER, Auteur ; Liesbeth ROOMS, Auteur ; R. Frank KOOY, Auteur Année de publication : 2012 Article en page(s) : p.277-81 Langues : Anglais (eng) Mots-clés : language delay autism ASD CMIP intellectual disability Index. décimale : PER Périodiques Résumé : In a developmentally delayed girl with an autism spectrum disorder, Single nucleotide polymorphism (SNP) array analysis showed a de novo 280 kb deletion on chromosome 16q23.2 involving two genes, GAN and CMIP. Inactivating mutations in GAN cause the autosomal recessive disorder giant axonal neuropathy, not present in our patient. CMIP was recently implicated in the etiology of specific language impairment by genome-wide association analysis. It modulates phonological short-term memory and hence plays an important role in language acquisition. Overlaps of specific language impairment and autism have been debated in the literature regarding the phenotypical language profile as well as etiology. Our patient illustrates that haploinsufficiency of CMIP may contribute to autism spectrum disorders. Our finding further supports the existence of a genetic overlap in the etiology of specific language impairment and autism. En ligne : http://dx.doi.org/10.1002/aur.1240 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=179
in Autism Research > 5-4 (August 2012) . - p.277-81[article] Haploinsufficiency of CMIP in a Girl With Autism Spectrum Disorder and Developmental Delay due to a De Novo Deletion on Chromosome 16q23.2 [Texte imprimé et/ou numérique] / Nathalie VAN DER AA, Auteur ; Geert VANDEWEYER, Auteur ; Edwin REYNIERS, Auteur ; Sandra KENIS, Auteur ; Lina DOM, Auteur ; Geert MORTIER, Auteur ; Liesbeth ROOMS, Auteur ; R. Frank KOOY, Auteur . - 2012 . - p.277-81.
Langues : Anglais (eng)
in Autism Research > 5-4 (August 2012) . - p.277-81
Mots-clés : language delay autism ASD CMIP intellectual disability Index. décimale : PER Périodiques Résumé : In a developmentally delayed girl with an autism spectrum disorder, Single nucleotide polymorphism (SNP) array analysis showed a de novo 280 kb deletion on chromosome 16q23.2 involving two genes, GAN and CMIP. Inactivating mutations in GAN cause the autosomal recessive disorder giant axonal neuropathy, not present in our patient. CMIP was recently implicated in the etiology of specific language impairment by genome-wide association analysis. It modulates phonological short-term memory and hence plays an important role in language acquisition. Overlaps of specific language impairment and autism have been debated in the literature regarding the phenotypical language profile as well as etiology. Our patient illustrates that haploinsufficiency of CMIP may contribute to autism spectrum disorders. Our finding further supports the existence of a genetic overlap in the etiology of specific language impairment and autism. En ligne : http://dx.doi.org/10.1002/aur.1240 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=179 Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder / Kumiko YANAGI in Autism Research and Treatment, (May 2012)
PermalinkImmune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder / Paula S. RAMOS in Molecular Autism, (June 2012)
PermalinkL’incidence des nouvelles connaissances génétiques et les nouveaux dialogues / François VITTECOQ
PermalinkIntégrer l’hétérogénéité clinique et génétique dans l’autisme / Michael L. CUCCARO
PermalinkInteraction between Genetic Vulnerability and Neurosteroids in Purkinje cells as a Possible Neurobiological Mechanism in Autism Spectrum Disorders / Flavio KELLER
PermalinkInteraction of dopamine transporter (DAT1) genotype and maltreatment for ADHD: a latent class analysis / James J. LI in Journal of Child Psychology and Psychiatry, 53-9 (September 2012)
PermalinkInteractions gènes-environnement dans la pathogénie / Marcello D’AMELIO
PermalinkInterparental conflict, parent psychopathology, hostile parenting, and child antisocial behavior: Examining the role of maternal versus paternal influences using a novel genetically sensitive research design / Gordon T. HAROLD in Development and Psychopathology, 24-4 (November 2012)
PermalinkIntroduction / Mary COLEMAN
PermalinkIs Autism a Common Personality Trait? / John N. CONSTANTINO
Permalink