Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Fabien Mourre"'
Autor:
Gwenaelle Diene, Christine Merrien, Virginie Laurier, Grégoire Benvegnu, Ana Camarena Toyos, Muriel Coupaye, Maithé Tauber, Graziella Pinto, Fabien Mourre, P Faucher, Héléna Mosbah, Laura González Briceño, Emilie Montastier, Christine Poitou
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2021, 16, pp.325. ⟨10.1186/s13023-021-01949-4⟩
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Orphanet Journal of Rare Diseases, 2021, 16, pp.325. ⟨10.1186/s13023-021-01949-4⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2021, 16, pp.325. ⟨10.1186/s13023-021-01949-4⟩
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Orphanet Journal of Rare Diseases, 2021, 16, pp.325. ⟨10.1186/s13023-021-01949-4⟩
Background Patients with Prader-Willi syndrome (PWS) often have comorbidities, especially obesity, that may constitute a risk factor for severe forms of COVID-19. We aimed to assess prevalence and medical course of SARS-CoV-2 infection in children an
Autor:
J. Jauregi, Geneviève Demeer, Pierre Copet, Denise Thuilleaux, Virginie Laurier, Fabien Mourre, Maithé Tauber, Julie Tricot
Publikováno v:
American Journal of Medical Genetics Part A. 176:41-47
High prevalence of behavioral and psychiatric disorders in adults with Prader-Willi Syndrome (PWS) has been reported in last few years. However, data are confusing and often contradictory. In this article, we propose a model to achieve a better under