Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Denise, Thuilleaux"'
Autor:
Kuzma Strenilkov, Jimmy Debladis, Juliette Salles, Marion Valette, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract 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, i
Externí odkaz:
https://doaj.org/article/1f3b3d235f8d4386a0fa41da577da8a7
Autor:
Jimmy Debladis, Marion Valette, Kuzma Strenilkov, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-13 (2019)
Abstract Background Faces are critical social cues that must be perfectly processed in order to engage appropriately in everyday social interactions. In Prader-Willi Syndrome (PWS), a rare genetic disorder characterized by cognitive and behavioural d
Externí odkaz:
https://doaj.org/article/120d85666e6c44a9aeff658126efa733
Autor:
Dibia Liz Pacoricona Alfaro, Perrine Lemoine, Virginie Ehlinger, Catherine Molinas, Gwénaëlle Diene, Marion Valette, Graziella Pinto, Muriel Coupaye, Christine Poitou-Bernert, Denise Thuilleaux, Catherine Arnaud, Maithé Tauber
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract 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. O
Externí odkaz:
https://doaj.org/article/27ec6559798c4c7590374449af42f65d
Autor:
Salles, Juliette, Strelnikov, Kuzma, Carine, Mantoulan, Denise, Thuilleaux, Laurier, Virginie, Molinas, Catherine, Tauber, Maïthé, Barone, Pascal
Publikováno v:
In Neuropsychologia May 2016 85:137-147
Autor:
Soraya Allas, Assumpta Caixàs, Christine Poitou, Muriel Coupaye, Denise Thuilleaux, Françoise Lorenzini, Gwenaëlle Diene, Antonino Crinò, Frédéric Illouz, Graziano Grugni, Diane Potvin, Sarah Bocchini, Thomas Delale, Thierry Abribat, Maithé Tauber
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0190849 (2018)
Prader-Willi syndrome (PWS) is characterized by early-onset hyperphagia and increased circulating levels of the orexigenic Acylated Ghrelin (AG) hormone with a relative deficit of Unacylated Ghrelin (UAG). AZP-531, a first-in-class UAG analog, was sh
Externí odkaz:
https://doaj.org/article/ff6cefe6e0af477b8ee96a2778760a9d
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:
Denise Thuilleaux, Virginie Postal, Anna-Malika Camblats, Virginie Laurier, Johann Chevalère, Maite Tauber
Publikováno v:
Advances in Mental Health and Intellectual Disabilities. 14:273-285
Purpose When a comprehensive neuropsychological assessment cannot be carried out, a quick and discriminant tool of good psychometric properties can be useful to practitioners. The purpose of this paper is to examine the use of the Montreal Cognitive
Publikováno v:
La Revue du praticien. 70(10)
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