Prevention of raised low-density lipoprotein cholesterol in a patient with familial hypercholesterolaemia and lipoprotein lipase deficiency
- 1 May 1993
- journal article
- Published by Elsevier BV in The Lancet
- Vol. 341 (8853), 1119-1121
- https://doi.org/10.1016/0140-6736(93)93129-o
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- A Mutation in the Human Lipoprotein Lipase Gene as the Most Common Cause of Familial Chylomicronemia in French CanadiansThe New England Journal of Medicine, 1991
- Regression of Coronary Artery Disease as a Result of Intensive Lipid-Lowering Therapy in Men with High Levels of Apolipoprotein BThe New England Journal of Medicine, 1990
- A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries.JCI Insight, 1990
- Common low-density lipoprotein receptor mutations in the French Canadian population.JCI Insight, 1990
- Lipoprotein metabolism during acute inhibition of lipoprotein lipase in the cynomolgus monkey.JCI Insight, 1988