Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Joseba Jauregui"'
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
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:
Luis Stinus, Joseba Jauregui, J. M. Deminière, Timothy T. Hand, Michel Le Moal, Dominique Nadaud
Publikováno v:
Biological Psychiatry. 26:363-371
The behavioral effects of systemic heroin administration were examined in rats subjected to flupentixol impregnation prior to and during behavioral testing. In the first experiment, the dose of heroin required to produce a place preference was determ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ffdaca47852b2c6034676e808561aa3
https://doi.org/10.1016/0006-3223(89)90052-8
https://doi.org/10.1016/0006-3223(89)90052-8