Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Denise, Thuilleaux"'
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:
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:
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