Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Denise, Thuilleaux"'
Autor:
Muriel Coupaye, Denise Thuilleaux, Sophie Çabal Berthoumieu, Marie Raffin, Christine Poitou, Said Lebbah, Olivier Bonnot, Maithé Tauber, Angèle Consoli, Graziella Pinto, Noel Zahr, David Cohen
Publikováno v:
Translational Psychiatry
Translational Psychiatry, Nature Pub. Group, 2019, 9 (1), pp.274. ⟨10.1038/s41398-019-0597-0⟩
Translational Psychiatry, Vol 9, Iss 1, Pp 1-8 (2019)
Translational Psychiatry, Nature Pub. Group, 2019, 9 (1), pp.274. ⟨10.1038/s41398-019-0597-0⟩
Translational Psychiatry, Vol 9, Iss 1, Pp 1-8 (2019)
Prader–Willi Syndrome (PWS) is a rare genetic syndrome leading to severe behavioural disorders and mild cognitive impairment. The objective of this double-blind randomised placebo-controlled trial was to study the efficacy and tolerance of topirama
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0dd1c7743421afd815425dffa1ff20c
https://hal.sorbonne-universite.fr/hal-02409179
https://hal.sorbonne-universite.fr/hal-02409179
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
Autor:
Virginie Ehlinger, Gwenaelle Diene, Catherine Molinas, Catherine Arnaud, Maithé Tauber, Dibia Liz Pacoricona Alfaro, Perrine Lemoine, Denise Thuilleaux, Christine Poitou-Bernert, Graziella Pinto, Muriel Coupaye, Marion Valette
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Orphanet Journal of Rare Diseases, BioMed Central, 2019, 14, pp.238. ⟨10.1186/s13023-019-1214-2⟩
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Orphanet Journal of Rare Diseases, BioMed Central, 2019, 14, pp.238. ⟨10.1186/s13023-019-1214-2⟩
Background In the last 20 years, substantial improvements have been made in the diagnosis, treatment and management of patients with Prader-Willi syndrome (PWS). Few data on causes of death are available since those improvements were made. Our study
Autor:
Thierry Abribat, Christine Poitou, Thomas Delale, Gwenaelle Diene, Frederic Illouz, Assumpta Caixàs, Muriel Coupaye, Diane Potvin, Françoise Lorenzini, Denise Thuilleaux, Graziano Grugni, Sarah Bocchini, Soraya Allas, Maithé Tauber, Antonino Crinò
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0190849 (2018)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
PLoS ONE
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
PLoS ONE
Altres ajuts: This study was supported by Alizé Pharma, sponsor of the trial (EudraCT: 2014- 001670-34). The sponsor Alizé Pharma was involved in the design of the study, data collection and analysis, decision to publish, and preparation of the man
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
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