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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Detalhes bibliográficos
Publicado no:Mol Genet Metab Rep
Main Authors: Mitja, Jevnikar, Metka, Kodric, Fabiana, Cantarutti, Cifaldi, Rossella, Longo, Cinzia, Rossana, Della Porta, Bruno, Bembi, Marco, Confalonieri
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2015
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5471388/
https://ncbi.nlm.nih.gov/pubmed/28649546
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2015.09.007
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