Alglucosidase alfa: Long term use in the treatment of patients with Pompe disease

• প্রধান লেখক: Michael Beck (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Dove Medical Press, 2009-09-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

Michael BeckChildren’s Hospital, University of Mainz, Mainz, GermanyAbstract: Pompe disease is a lysosomal storage disorder characterized by muscle weakness and cardiomyopathy. It shows a broad variability regarding the clinical severity as well as the age of onset. In the past, two differ...