Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Denise, Thuilleaux"'
Autor:
Maithé Tauber, A.-M. Camblats, Virginie Postal, Virginie Laurier, J. Chevalère, Denise Thuilleaux
Publikováno v:
Journal of Intellectual & Developmental Disability. 47:18-26
The present study investigated decision-making in patients with Prader-Willi syndrome (PWS) using the Soochow Gambling Task (SGT). The objective was to assess whether adults with PWS have impaired ...
Autor:
Virginie Postal, Denise Thuilleaux, Virginie Laurier, Séverine Estival, Agata Krasny-Pacini, Céline Maugard
Publikováno v:
Developmental Neurorehabilitation
Developmental Neurorehabilitation, Informa Healthcare, 2019, 22 (8), pp.569-575. ⟨10.1080/17518423.2019.1642414⟩
Developmental Neurorehabilitation, Informa Healthcare, 2019, 22 (8), pp.569-575. ⟨10.1080/17518423.2019.1642414⟩
Background: Prader-Willi syndrome (PWS) is a neurodevelopmental genetic disorder involving executive deficits notably with planning. The main objective of the study is to assess the effectiveness of cognitive training on daily life planning difficult
Autor:
Marion Valette, Maithé Tauber, Carine Mantoulan, Kuzma Strenilkov, Pascal Barone, Denise Thuilleaux, Juliette Salles, Virginie Laurier, Catherine Molinas, Jimmy Debladis
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15, ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15, ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Background Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ba7378a79e3d8f08bf9d9f0398b7fe9
https://hal.archives-ouvertes.fr/hal-03093987
https://hal.archives-ouvertes.fr/hal-03093987
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:
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
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