𝔖 Bobbio Scriptorium
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QUANTITATIVE MORPHOLOGY OF MUSCLE IN INFANTILE MALNUTRITION

Book ID
114909024
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
147 KB
Volume
37
Category
Article
ISSN
0029-6643

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Morphological changes in muscle tissue o
Morphological changes in muscle tissue of patients with infantile Pompe's disease receiving enzyme replacement therapy
✍ LΓ©on P. F. Winkel; Joep H. J. Kamphoven; Hannerieke J. M. P. Van Den Hout; Lies πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 621 KB

## Abstract Pompe's disease (glycogen storage disease type II) is an autosomal recessive myopathy caused by lysosomal α‐glucosidase deficiency. Enzyme replacement therapy (ERT) is currently under development for this disease. We evaluated the morphological changes in muscle tissue of four children