Cargando…
A study of voice and non-voice processing in Prader-Willi syndrome
BACKGROUND: Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired acquisition of social and communication skills lea...
Autores principales: | Strenilkov, Kuzma, Debladis, Jimmy, Salles, Juliette, Valette, Marion, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Tauber, Maïthé |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972021/ https://www.ncbi.nlm.nih.gov/pubmed/31959191 http://dx.doi.org/10.1186/s13023-020-1298-8 |
Ejemplares similares
-
Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature
por: Debladis, Jimmy, et al.
Publicado: (2019) -
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients
por: Tauber, Maïthe, et al.
Publicado: (2011) -
Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables
por: Jauregi, Joseba, et al.
Publicado: (2013) -
Causes of death in Prader-Willi syndrome: lessons from 11 years’ experience of a national reference center
por: Pacoricona Alfaro, Dibia Liz, et al.
Publicado: (2019) -
Is ghrelin a biomarker of early-onset scoliosis in children with Prader–Willi syndrome?
por: Pacoricona Alfaro, Dibia Liz, et al.
Publicado: (2021)