Documents Clinical guidelines for late-onset Pompe disease

GUIDELINES Introduction Glycogen storage disease type II or Pompe disease (OMIM Entry # 232300), also referred to as acid maltase deficiency, is a rare lysosomal storage

Documents A Systematic Review and Meta-Analysis of Enzyme Replacement Therapy in Late-Onset Pompe Disease

A Systematic Review and Meta-Analysis of Enzyme Replacement Therapy in Late-Onset Pompe DiseaseA Systematic Review and Meta-Analysis of Enzyme Replacement Therapy in Late-Onset