Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fabien Mourre"'
Publikováno v:
Developmental Neurorehabilitation. 24:478-493
Prader-Willi Syndrome (PWS) is a neurodevelopmental genetic disorder with executive deficits. Planning is one of the impaired executive functions implied in the regulation of behavior and everyday actions. We aimed to explore the feasibility and the
Autor:
Gwenaelle Diene, Fabien Mourre, Alice Clerc, Graziella Pinto, Maithé Tauber, Christine Poitou, Héléna Mosbah, Virginie Laurier, Muriel Coupaye, Christine Merrien
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, MDPI, 2021, 10 (22), pp.5310. ⟨10.3390/jcm10225310⟩
Volume 10
Issue 22
Journal of Clinical Medicine, 2021, 10 (22), pp.5310. ⟨10.3390/jcm10225310⟩
Journal of Clinical Medicine, Vol 10, Iss 5310, p 5310 (2021)
Journal of Clinical Medicine, MDPI, 2021, 10 (22), pp.5310. ⟨10.3390/jcm10225310⟩
Volume 10
Issue 22
Journal of Clinical Medicine, 2021, 10 (22), pp.5310. ⟨10.3390/jcm10225310⟩
Journal of Clinical Medicine, Vol 10, Iss 5310, p 5310 (2021)
Type 2 diabetes mellitus (T2DM) affects 20% of patients with Prader-Willi syndrome (PWS), with many cases diagnosed during the transition period. Our aim was to describe the natural history of T2DM in patients with PWS before the age of 25 years and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::505394040ed810d46adec675f3e0443a
https://hal.sorbonne-universite.fr/hal-03457276
https://hal.sorbonne-universite.fr/hal-03457276
Autor:
Séverine Estival, Johann Chevalère, Julie Tricot, Virginie Laurier, Virginie Postal, Fabien Mourre
Publikováno v:
Research in Developmental Disabilities. 117:104056
Background Prader-Willi syndrome (PWS) is a complex developmental genetic disorder associated with intellectual disability and deficits in executive functions which result in disorganisation and poor personal autonomy. Aims This study aimed to determ