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Reversal of Cardiac Dysfunction after Enzyme Replacement in Patients with Infantile-Onset Pompe Disease

✍ Scribed by Lei-Ru Chen; Chun-An Chen; Shuenn-Nan Chiu; Yin-Hsiu Chien; Ni-Chung Lee; Ming-Tai Lin; Wuh-Liang Hwu; Jou-Kou Wang; Mei-Hwan Wu


Book ID
113745263
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
317 KB
Volume
155
Category
Article
ISSN
1097-6833

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Morphological changes in muscle tissue o
✍ 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