Výsledky vyhledávání - "Pierre Copet"

A model to characterize psychopathological features in adults with Prader-Willi syndrome

Autor: J. Jauregi, Geneviève Demeer, Pierre Copet, Denise Thuilleaux, Virginie Laurier, Fabien Mourre, Maithé Tauber, Julie Tricot

Publikováno v: American Journal of Medical Genetics Part A. 176:41-47

High prevalence of behavioral and psychiatric disorders in adults with Prader-Willi Syndrome (PWS) has been reported in last few years. However, data are confusing and often contradictory. In this article, we propose a model to achieve a better under

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::036b610a78555a8ed43686087f77faf0
https://doi.org/10.1002/ajmg.a.38525

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Executive Functions and Prader-Willi Syndrome: Global Deficit Linked With Intellectual Level and Syndrome-Specific Associations

Autor: Joseba Jauregui, Virginie Laurier, Pierre Copet, Virginie Postal, Johann Chevalère, Denise Thuilleaux

Publikováno v: American Journal on Intellectual and Developmental Disabilities
American Journal on Intellectual and Developmental Disabilities, American Association on Intellectual and Developmental Disabilities Allen Press, Inc., 2015, 120 (3), pp.215-229. ⟨10.1352/1944-7558-120.3.215⟩

The aim of this study was to support the growing evidence suggesting that Prader-Willi Syndrome (PWS) might present with an impairment of executive functions (EFs) and to investigate whether this impairment is specific to patients with PWS or due to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7870df3ae39cbd26244ddaa756b405cc
https://hal.archives-ouvertes.fr/hal-03245227

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Assessment of executive functions in Prader-Willi syndrome and relationship with intellectual level

Autor: Pierre Copet, Denise Thuilleaux, Virginie Postal, Virginie Laurier, Johann Chevalère, Joseba Jauregui

Publikováno v: Journal of applied research in intellectual disabilities : JARID. 26(4)

Introduction The aim of the present study was to determine whether individuals with Prader–Willi syndrome (PWS) have impaired global executive functioning and whether this deficit is linked with intellectual disability. Another objective focussed o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f378b9eb001de816db6ca63643ec8e9e
https://pubmed.ncbi.nlm.nih.gov/23606605

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Behavioral profile of adults with Prader-Willi syndrome : correlations with individual and environmental variables

Autor: Pierre Copet, Virginie Laurier, J. Jauregi, Denise Thuilleaux, Maithé Tauber

Publikováno v: Addi. Archivo Digital para la Docencia y la Investigación
instname
Journal of Neurodevelopmental Disorders

BackgroundMaladaptive behavior has been reported as a phenotypical feature in Prader–Willi syndrome (PWS). It severely limits social adaptation and the quality of life of children and adults with the syndrome. Different factors have been linked wit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::420aefa6164bb86798408085f5f18d6e
http://hdl.handle.net/10810/11022

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Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients

Autor: Catherine Arnaud, Geneviève Demeer, Virginie Ehlinger, Virginie Laurier, Denise Thuilleaux, Maithé Tauber, Joseba Jauregui, Catherine Molinas, Carine Mantoulan, Bernadette Rogé, Gwenaelle Diene, Pierre Copet

Publikováno v: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.47. ⟨10.1186/1750-1172-6-47⟩
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 47 (2011)
Orphanet Journal of Rare Diseases, BioMed Central, 2011, 6 (1), pp.47. ⟨10.1186/1750-1172-6-47⟩

Background Prader-Willi syndrome (PWS) is a complex neurodevelopmental genetic disorder with hypothalamic dysfunction, early morbid obesity with hyperphagia, and specific psychiatric phenotypes including cognitive and behavioural problems, particular

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9dbdb5d90315dfb3b2102e76e16d50b
https://www.hal.inserm.fr/inserm-00663634/document

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