Výsledky vyhledávání - "Ioannis Arnaoutis"

Body composition and 6 minute walking ability in late-onset pompe disease patients after 9 years of enzyme replacement therapy

Autor: Gerasimos Terzis, Eleni Kontou, Georgios Papadimas, Constantinos Papadopoulos, Argyro Krase, Ioannis Arnaoutis

Publikováno v: International Journal of Neuroscience. 132:699-705

Pompe disease is a rare autosomal recessive disorder caused by the deficiency of acid α-glycosidase resulting in accumulation of glycogen in the lysosomes. The late-onset form of the disease (LOPD) causes primarily progressive muscle weakness and re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539cc9037dbcd5d8d2a0cc773991ddb9
https://doi.org/10.1080/00207454.2020.1835902

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