Zobrazeno 1 - 3
of 3
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:
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:
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