Paradoxical low severity of COVID-19 in Prader-Willi syndrome: data from a French survey on 647 patients

Autor: Muriel Coupaye, Virginie Laurier, Grégoire Benvegnu, Christine Poitou, Pauline Faucher, Héléna Mosbah, Gwenaelle Diene, Graziella Pinto, Laura González Briceño, Christine Merrien, Ana Camarena Toyos, Emilie Montastier, Maithé Tauber, Fabien Mourre

Publikováno v: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)

Abstract 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 ch

Externí odkaz: https://doaj.org/article/8f58e7b845b34f7f87cd95a1188c91d4

Improvement of Planning Abilities in Adults with Prader-Willi Syndrome: A Randomized Controlled Trial

Autor: Séverine Estival, Fabien Mourre, Virginie Postal, Virginie Laurier

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c50c373200f24cb50791a72cadb213af
https://doi.org/10.1080/17518423.2021.1915405

Paradoxical low severity of COVID-19 in Prader-Willi syndrome: data from a French survey on 647 patients

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⟩

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66f9233e47bd23742a1ea06801a485f6
https://pubmed.ncbi.nlm.nih.gov/34289876

Study of the deficit in planning abilities of adults with Prader-Willi Syndrome

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e525da61a9cd23092b99f88a68fbf29d
https://doi.org/10.1016/j.ridd.2021.104056

Optimization of the use of B-type natriuretic peptide levels for risk stratification at discharge in elderly patients with decompensated heart failure

Autor: Sylvain Destrac, Fabien Mourre, Maxime Cournot, Jean Ferrières, Fabienne Castel

Publikováno v: American Heart Journal. 155:986-991

In elderly patients hospitalized for decompensated heart failure, B-type natriuretic peptide (BNP) levels at discharge and the change in BNP during hospitalization may provide different information and may need to be taken into account simultaneously

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d55520e59dbff4e1f723cbf02c69d34
https://doi.org/10.1016/j.ahj.2008.01.011