"Glycogen Storage Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
|Glycogen Storage Disease
- Glycogen Storage Disease
- Disease, Glycogen Storage
- Diseases, Glycogen Storage
- Glycogen Storage Diseases
- Storage Disease, Glycogen
- Storage Diseases, Glycogen
Below are MeSH descriptors whose meaning is more general than "Glycogen Storage Disease".
Below are MeSH descriptors whose meaning is more specific than "Glycogen Storage Disease".
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Below are the most recent publications written about "Glycogen Storage Disease" by people in Profiles.
Polyglucosan bodies in intramuscular nerve branches are a poor predictor of GBE1 mutation and adult polyglucosan body disease. Muscle Nerve. 2016 Mar; 53(3):473-5.
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy. Circulation. 2003 Jun 10; 107(22):2850-6.
Evaluation of the lumbar spine in patients with glycogen storage disease: CT demonstration of patterns of paraspinal muscle atrophy. AJNR Am J Neuroradiol. 1991 Nov-Dec; 12(6):1099-103.
Pompe's disease in identical twins. Hosp Pract (Off Ed). 1986 Mar 30; 21(3A):146-8, 153, 156-8.
A comparative study of three methods for the ultrastructural demonstration of glycogen in thin sections. J Cell Sci. 1971 Nov; 9(3):727-49.