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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Detalhes bibliográficos
Publicado no:Health Qual Life Outcomes
Main Authors: Powell, Philip A., Carlton, Jill, Woods, Helen Buckley, Mazzone, Paolo
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Review
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7397669/
https://ncbi.nlm.nih.gov/pubmed/32746836
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12955-020-01511-z
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