Glycogen Storage Disease Type III diagnosis and management guidelines

The electrodiagnostic characteristics of Glycogen Storage Disease Type III

(2010) Lisa D Hobson-Webb et al.   GENETICS IN MEDICINE

Echocardiographic manifestations of Glycogen Storage Disease III: Increase in wall thickness and left ventricular mass over time

(2010) Shawyntee M Vertilus et al.   GENETICS IN MEDICINE

Molecular analysis of the AGL gene: Identification of 25 novel mutations and evidence of genetic heterogeneity in patients with Glycogen Storage Disease Type III

(2010) Jennifer L Goldstein et al.   GENETICS IN MEDICINE

Distinct mutations in the glycogen debranching enzyme found in glycogen storage disease type III lead to impairment in diverse cellular functions

(2009) Alan Cheng et al.   HUMAN MOLECULAR GENETICS

Pompe disease: A neuromuscular disease with respiratory muscle involvement

(2009) Uwe Mellies et al.   RESPIRATORY MEDICINE

Reduction in bone mineral density in glycogenosis type III may be due to a mixed muscle and bone deficit

(2008) H. R. Mundy et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Cardiac Remodeling After Enzyme Replacement Therapy with Acid α-Glucosidase for Infants with Pompe Disease

(2008) Jami C. Levine et al.   PEDIATRIC CARDIOLOGY

Liver transplantation in children with glycogen storage disease: Controversies and evaluation of the risk/benefit of this procedure

(2008) Michael K. Davis et al.   PEDIATRIC TRANSPLANTATION