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urea and Lecithin Cholesterol Acyltransferase Deficiency

urea has been researched along with Lecithin Cholesterol Acyltransferase Deficiency in 1 studies

pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.

Lecithin Cholesterol Acyltransferase Deficiency: An autosomal recessive disorder of lipoprotein metabolism caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE gene. It is characterized by low HDL-cholesterol levels, and the triad of CORNEAL OPACITIES; HEMOLYTIC ANEMIA; and PROTEINURIA with renal failure.

Research

Studies (1)

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

Authors

AuthorsStudies
Gillett, MP1
Teixeira, V1
Dimenstein, R1

Other Studies

1 other study available for urea and Lecithin Cholesterol Acyltransferase Deficiency

ArticleYear
Decreased plasma lecithin:cholesterol acyltransfer and associated changes in plasma and red cell lipids in uraemia.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 1993, Volume: 8, Issue:5

    Topics: Adult; Erythrocytes; Female; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lipids; Male;

1993