choline has been researched along with Lecithin Cholesterol Acyltransferase Deficiency in 1 studies
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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 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 |
|---|---|
| O, K | 1 |
| Ly, M | 1 |
| Fang, DZ | 1 |
| Frohlich, J | 1 |
| Choy, PC | 1 |
1 other study available for choline and Lecithin Cholesterol Acyltransferase Deficiency
| Article | Year |
|---|---|
Effect of lipoprotein-X on lipid metabolism in rat kidney.
Topics: 1-Acylglycerophosphocholine O-Acyltransferase; Acetates; Animals; Choline; Humans; Kidney; Lecithin | 1997 |