Friedrich-Baur-Institut Neurologische Klinik Ludwig-Maximilians-Universität München

München D08033

0 studies enrolling now · 1 studies all time

What they study most

Acid Maltase Deficiency, Glycogen Storage Disease Type 2, Glycogen Storage Disease Type II, LOPD, Lysosomal Storage Diseases, Pompe Disease, Pompe Disease (Late-onset)

Studies at this site

• A Gene Transfer Study for Late-Onset Pompe Disease (RESOLUTE) — Running, not enrolling