Harvard Catalyst Profiles

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Glycogen Storage Disease Type I

"Glycogen Storage Disease Type I" 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.

An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.


This graph shows the total number of publications written about "Glycogen Storage Disease Type I" by people in Harvard Catalyst Profiles by year, and whether "Glycogen Storage Disease Type I" was a major or minor topic of these publication.
Bar chart showing 29 publications over 18 distinct years, with a maximum of 5 publications in 2002
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.