What Happens After a Pompe Disease Diagnosis
What is Pompe disease: 5 things to know about the rare gene mutation
Effect of alglucosidase alfa dosage on survival and walking ability in patients with classic infantile Pompe disease: a multicentre observational cohort study from the European Pompe Consortium - The Lancet Child &
Learn more about Pompe disease
Cardiac outcome in classic infantile Pompe disease after 13 years of treatment with recombinant human acid alpha-glucosidase - International Journal of Cardiology
Pompe Disease: The Story Behind the Movie | Duke Today
Gene Therapy for Pompe Disease Effective in Mice, Poised for Human Trials | Duke Health
Outcome of Later-Onset Pompe Disease Identified Through Newborn Screening - The Journal of Pediatrics
The molecular basis for Pompe disease revealed by the structure of human acid α-glucosidase | bioRxiv
Pompe Disease: Causes Types Symptoms Signs Diagnosis Treatment FAQs
Failure to Thrive in Babies and Pompe Disease — Genepath
Non-specificity of symptoms in infantile-onset Pompe disease may delay the diagnosis and institution of treatment | BMJ Case Reports
Clinical guidelines for late-onset Pompe disease
Is it Pompe Disease? Australian diagnostic considerations - Neuromuscular Disorders
Glycogen storage disease type II - Wikipedia
Pompe Disease: a Clinical, Diagnostic, and Therapeutic Overview | SpringerLink
Pompe disease: pathogenesis, molecular genetics and diagnosis | Aging
Pompe Disease (also called Glycogen storage disease type 2) | CheckRare
A Skeletal Muscle Model of Infantile-onset Pompe Disease with Patient-specific iPS Cells | Scientific Reports
Infantile-onset Pompe May Be Evident in Fluid Build-up in Newborns, Case Study Says
Rescue of Advanced Pompe Disease in Mice with Hepatic Expression of Secretable Acid α-Glucosidase: Molecular Therapy
Causes of Pompe Disease | GAA Mutations and Inheritance | Pompe Disease News
