Medication Trials for Hyperphagia and Food-Related Behaviors in Prader–Willi Syndrome

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally expressed, imprinted genes on chromosome 15q11-13. Individuals with PWS characteristically have poor feeding and lack of appetite in infancy, followed by the development of weight gain and then uncontrol...

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Detalles Bibliográficos
Autores principales: Miller, Jennifer L., Strong, Theresa V., Heinemann, Janalee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548239/
https://www.ncbi.nlm.nih.gov/pubmed/28943610
http://dx.doi.org/10.3390/diseases3020078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548239/
https://www.ncbi.nlm.nih.gov/pubmed/28943610
http://dx.doi.org/10.3390/diseases3020078

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