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Publications by P Blümel
Mutations in the Liver Glycogen Synthase Gene in Children With Hypoglycemia Due to Glycogen Storage Disease Type 0.
Journal of Clinical Investigation
Medicine
Related publications
Glycogen Storage Disease Due to Muscle and Heart Glycogen Synthase Deficiency
Orthotopic Liver Transplantation in Glycogen Storage Disease Type 1a
Journal of Inborn Errors of Metabolism and Screening
Child Health
Genetics
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Hepatic and Neuromuscular Forms of Glycogen Storage Disease Type IV Caused by Mutations in the Same Glycogen-Branching Enzyme Gene.
Journal of Clinical Investigation
Medicine
Novel PYGL Mutations in Chinese Children Leading to Glycogen Storage Disease Type VI: Two Case Reports
BMC Medical Genetics
Genetics
Glycogen Storage Disease Due to Phosphorylase Kinase Deficiency
Glycogen Storage Disease Due to LAMP-2 Deficiency
The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23
American Journal of Human Genetics
Genetics
Glycogen Storage Disease Due to Muscle Phosphorylase Kinase Deficiency
Liver Glycogen Storage in Diabetic Animals
American Journal of Physiology-Legacy Content
