Patient Reported Outcome Measures in Adult Spinal Muscular Atrophy: A Scoping Review and Graphical Visualization of the Evidence

BACKGROUND: Spinal Muscular Atrophy (SMA) is a hereditary neuromuscular disease with an estimated prevalence of 1/10 000 births. SMA is increasingly recognized as a multi-system disease with a need to study additional under-recognized health domains such as quality of life, fatigue, bulbar function,...

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Detalles Bibliográficos
Autores principales: Slayter, Jeremy, Casey, Lauren, O’Connell, Colleen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041426/
https://www.ncbi.nlm.nih.gov/pubmed/36530090
http://dx.doi.org/10.3233/JND-221595

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041426/
https://www.ncbi.nlm.nih.gov/pubmed/36530090
http://dx.doi.org/10.3233/JND-221595

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