histamine has been researched along with Telangiectasia, Hereditary Hemorrhagic in 2 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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
LivandovskiÄ, IuA | 2 |
Fedorova, NV | 1 |
1 review available for histamine and Telangiectasia, Hereditary Hemorrhagic
Article | Year |
---|---|
[Pathogenesis of Osler-Rendu disease].
Topics: Blood Pressure; Capillaries; Dilatation, Pathologic; Elastic Tissue; Histamine; Humans; Pancreatic E | 1980 |
1 other study available for histamine and Telangiectasia, Hereditary Hemorrhagic
Article | Year |
---|---|
[Biogenic amines (serotonin and histamine) in Rendu-Osler disease].
Topics: Adult; Aged; Female; Histamine; Humans; Male; Middle Aged; Serotonin; Telangiectasia, Hereditary Hem | 1975 |