Page last updated: 2024-10-25

clonidine and Telangiectasia, Hereditary Hemorrhagic

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

Clonidine: An imidazoline sympatholytic agent that stimulates ALPHA-2 ADRENERGIC RECEPTORS and central IMIDAZOLINE RECEPTORS. It is commonly used in the management of HYPERTENSION.
clonidine (amino form) : A clonidine that is 4,5-dihydro-1H-imidazol-2-amine in which one of the amino hydrogens is replaced by a 2,6-dichlorophenyl group.

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-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Endo, Y1
Miura, A1

Other Studies

1 other study available for clonidine and Telangiectasia, Hereditary Hemorrhagic

ArticleYear
[Platelet function and catecholamines].
    Rinsho byori. The Japanese journal of clinical pathology, 1989, Volume: 37, Issue:1

    Topics: Adenosine Diphosphate; Adolescent; Adult; Aged; Clonidine; Epinephrine; Female; Humans; Male; Middle

1989