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

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

Open source

DOI
10.1186/s13023-021-01949-4
Published
2021-07-21
Container
Orphanet Journal of Rare Diseases
Publisher
Springer Science and Business Media LLC
Open access
unknown

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BibTeX

@article{allodium:10.1186/s13023-021-01949-4,
  title = {Paradoxical low severity of COVID-19 in Prader-Willi syndrome: data from a French survey on 647 patients},
  author = {Muriel Coupaye and Virginie Laurier and Grégoire Benvegnu and Christine Poitou and Pauline Faucher and Héléna Mosbah and Gwenaelle Diene and Graziella Pinto and Laura González Briceño and Christine Merrien and Ana Camarena Toyos and Emilie Montastier and Maithé Tauber and Fabien Mourre},
  year = {2021},
  journal = {Orphanet Journal of Rare Diseases},
  doi = {10.1186/s13023-021-01949-4},
  url = {https://doi.org/10.1186/s13023-021-01949-4}
}

RIS

TY  - JOUR
TI  - Paradoxical low severity of COVID-19 in Prader-Willi syndrome: data from a French survey on 647 patients
AU  - Muriel Coupaye
AU  - Virginie Laurier
AU  - Grégoire Benvegnu
AU  - Christine Poitou
AU  - Pauline Faucher
AU  - Héléna Mosbah
AU  - Gwenaelle Diene
AU  - Graziella Pinto
AU  - Laura González Briceño
AU  - Christine Merrien
AU  - Ana Camarena Toyos
AU  - Emilie Montastier
AU  - Maithé Tauber
AU  - Fabien Mourre
PY  - 2021
JO  - Orphanet Journal of Rare Diseases
DO  - 10.1186/s13023-021-01949-4
UR  - https://doi.org/10.1186/s13023-021-01949-4
ER  - 

APA

Coupaye, M., Laurier, V., Benvegnu, G., Poitou, C., Faucher, P., Mosbah, H., Diene, G., Pinto, G., Briceño, L. G., Merrien, C., Toyos, A. C., Montastier, E., Tauber, M., & Mourre, F. (2021). Paradoxical low severity of COVID-19 in Prader-Willi syndrome: data from a French survey on 647 patients. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-021-01949-4

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