Harvard Catalyst Profiles

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Telangiectasia, Hereditary Hemorrhagic

"Telangiectasia, Hereditary Hemorrhagic" 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 dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA.


This graph shows the total number of publications written about "Telangiectasia, Hereditary Hemorrhagic" by people in Harvard Catalyst Profiles by year, and whether "Telangiectasia, Hereditary Hemorrhagic" was a major or minor topic of these publication.
Bar chart showing 51 publications over 21 distinct years, with a maximum of 4 publications in 2006 and 2009 and 2012 and 2015
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.