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Successful pregnancy outcome in a patient with Fabry disease receiving enzyme replacement therapy with agalsidase alfa

✍ Scribed by S. Wendt; C. Whybra; C. Kampmann; E. Teichmann; M. Beck


Publisher
Springer
Year
2005
Tongue
English
Weight
83 KB
Volume
28
Category
Article
ISSN
0141-8955

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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