Page last updated: 2024-10-29

ioversol and Telangiectasia, Hereditary Hemorrhagic

ioversol has been researched along with Telangiectasia, Hereditary Hemorrhagic in 1 studies

Telangiectasia, Hereditary Hemorrhagic: 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.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lin, E1
Stall, L1

Other Studies

1 other study available for ioversol and Telangiectasia, Hereditary Hemorrhagic

ArticleYear
Spectrum of biliary abnormalities in hepatic hereditary hemorrhagic telangiectasia: demonstration by multidetector computed tomography.
    Emergency radiology, 2007, Volume: 14, Issue:6

    Topics: Aged; Biliary Tract Diseases; Contrast Media; Female; Humans; Liver Function Tests; Telangiectasia,

2007