Measuring quality of life in Duchenne muscular dystrophy: a systematic review of the content and structural validity of commonly used instruments

Duchenne muscular dystrophy (DMD) is an inherited X-linked neuromuscular disorder. A number of questionnaires are available to assess quality of life in DMD, but there are concerns about their validity. This systematic review aimed to appraise critically the content and structural validity of qualit...

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Detalles Bibliográficos
Autores principales: Powell, Philip A., Carlton, Jill, Woods, Helen Buckley, Mazzone, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397669/
https://www.ncbi.nlm.nih.gov/pubmed/32746836
http://dx.doi.org/10.1186/s12955-020-01511-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397669/
https://www.ncbi.nlm.nih.gov/pubmed/32746836
http://dx.doi.org/10.1186/s12955-020-01511-z

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