Page last updated: 2024-10-30

losartan and Endocardial Fibroelastosis

losartan has been researched along with Endocardial Fibroelastosis in 1 studies

Losartan: An antagonist of ANGIOTENSIN TYPE 1 RECEPTOR with antihypertensive activity due to the reduced pressor effect of ANGIOTENSIN II.
losartan : A biphenylyltetrazole where a 1,1'-biphenyl group is attached at the 5-position and has an additional trisubstituted imidazol-1-ylmethyl group at the 4'-position

Endocardial Fibroelastosis: A condition characterized by the thickening of ENDOCARDIUM due to proliferation of fibrous and elastic tissue, usually in the left ventricle leading to impaired cardiac function (CARDIOMYOPATHY, RESTRICTIVE). It is most commonly seen in young children and rarely in adults. It is often associated with congenital heart anomalies (HEART DEFECTS CONGENITAL;) INFECTION; or gene mutation. Defects in the tafazzin protein, encoded by TAZ gene, result in a form of autosomal dominant familial endocardial fibroelastosis.

Research

Studies (1)

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

Authors

AuthorsStudies
Vorisek, C1
Weixler, V1
Dominguez, M1
Axt-Fliedner, R1
Hammer, PE1
Lin, RZ1
Melero-Martin, JM1
Del Nido, PJ1
Friehs, I1

Other Studies

1 other study available for losartan and Endocardial Fibroelastosis

ArticleYear
Mechanical strain triggers endothelial-to-mesenchymal transition of the endocardium in the immature heart.
    Pediatric research, 2022, Volume: 92, Issue:3

    Topics: Animals; Bone Morphogenetic Protein 7; Endocardial Fibroelastosis; Endocardium; Endothelial Cells; E

2022