French database of children and adolescents with Prader-Willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a rare multisystem genetic disease leading to severe complications mainly related to obesity. We strongly lack information on the natural history of this complex disease and on what factors are involved in its evolution and its outcome. One of the objective...

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Detalles Bibliográficos
Autores principales: Molinas, Catherine, Cazals, Laurent, Diene, Gwenaelle, Glattard, Melanie, Arnaud, Catherine, Tauber, Maithe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Database
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569911/
https://www.ncbi.nlm.nih.gov/pubmed/18831731
http://dx.doi.org/10.1186/1471-2350-9-89

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569911/
https://www.ncbi.nlm.nih.gov/pubmed/18831731
http://dx.doi.org/10.1186/1471-2350-9-89

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