Respiratory muscle training with enzyme replacement therapy improves muscle strength in late - onset Pompe disease

BACKGROUND: Pompe disease is an autosomal recessive metabolic disorder caused by the deficiency of the lysosomal enzyme acid α-glucosidase. This deficiency leads to glycogen accumulation in the lysosomes of muscle tissue causing progressive muscular weakness particularly of the respiratory system. E...

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Detalles Bibliográficos
Autores principales: Mitja, Jevnikar, Metka, Kodric, Fabiana, Cantarutti, Cifaldi, Rossella, Longo, Cinzia, Rossana, Della Porta, Bruno, Bembi, Marco, Confalonieri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471388/
https://www.ncbi.nlm.nih.gov/pubmed/28649546
http://dx.doi.org/10.1016/j.ymgmr.2015.09.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471388/
https://www.ncbi.nlm.nih.gov/pubmed/28649546
http://dx.doi.org/10.1016/j.ymgmr.2015.09.007

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