Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Pierre Copet"'
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
https://doi.org/10.1002/ajmg.a.38525
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⟩
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
https://hal.archives-ouvertes.fr/hal-03245227
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
https://pubmed.ncbi.nlm.nih.gov/23606605
Publikováno v:
Addi. Archivo Digital para la Docencia y la Investigación
instname
Journal of Neurodevelopmental Disorders
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
http://hdl.handle.net/10810/11022
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⟩
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
https://www.hal.inserm.fr/inserm-00663634/document
Autor:
Thuilleaux, Denise, Laurier, Virginie, Copet, Pierre, Tricot, Julie, Demeer, Geneviève, Mourre, Fabien, Tauber, Maithé, Jauregi, Joseba
Publikováno v:
American Journal of Medical Genetics. Part A; Jan2018, Vol. 176 Issue 1, p41-47, 7p
Autor:
Chevalère, Johann, Postal, Virginie, Jauregui, Joseba, Copet, Pierre, Laurier, Virginie, Thuilleaux, Denise
Publikováno v:
American Journal on Intellectual & Developmental Disabilities; May2015, Vol. 120 Issue 3, p215-229, 15p
Publikováno v:
American Journal on Intellectual & Developmental Disabilities; May2015, Vol. 120 Issue 3, p271-272, 2p
Publikováno v:
American Journal on Intellectual & Developmental Disabilities; May2015, Vol. 120 Issue 3, p269-270, 2p
Publikováno v:
Périodiques Scientifiques en Édition Électronique.
Là où l'histoire, par définition, est attentive aux évolutions, l'anthropologue recherche les permanences structurelles qui ouvrent à la comparaison. Le système de parenté à Rome est cognatique, comme l'est la gens, et la parenté reconnue de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______627::8079448c2a1b82f0e473600dedbd949a
https://www.persee.fr/doc/efr_0000-0000_1990_act_129_1_3790
https://www.persee.fr/doc/efr_0000-0000_1990_act_129_1_3790