The feasibility of using actigraphy to characterize sleep in Rett syndrome

BACKGROUND: Rett syndrome (RTT) is a neurodevelopmental disorder primarily caused by mutations in the MECP2 gene. Sleep problems are reported by the majority of caregivers of individuals with RTT. METHODS: The present study aimed to replicate and extend previous work about the feasibility of measuri...

Descripción completa

Detalles Bibliográficos
Autores principales: Merbler, Alyssa M., Byiers, Breanne J., Garcia, John J., Feyma, Timothy J., Symons, Frank J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828406/
https://www.ncbi.nlm.nih.gov/pubmed/29482495
http://dx.doi.org/10.1186/s11689-018-9227-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828406/
https://www.ncbi.nlm.nih.gov/pubmed/29482495
http://dx.doi.org/10.1186/s11689-018-9227-z

Ejemplares similares