Cargando...
Oxytocin treatment in children with Prader–Willi syndrome: A double-blind, placebo-controlled, crossover study
Prader–Willi syndrome (PWS) is a rare, complex multisystem genetic disorder which includes hypothalamic dysfunction, hyperphagia, cognitive and behavioral problems, increased anxiety, and compulsive behaviors. Individuals with PWS have a deficit of oxytocin producing neurons in the paraventricular n...
Guardado en:
| Publicado en: | Am J Med Genet A |
|---|---|
| Autores principales: | , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2017
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5828021/ https://ncbi.nlm.nih.gov/pubmed/28371242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38160 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|