Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics
- 15 July 1993
- journal article
- research article
- Published by Elsevier
- Vol. 72 (2) , 171-176
- https://doi.org/10.1016/0002-9149(93)90155-6
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Documented need for more effective diagnosis and treatment of familial hypercholesterolemia according to data from 502 heterozygotes in UtahThe American Journal of Cardiology, 1993
- Diagnosis of heterozygous familial hypercholesterolemia. DNA analysis complements clinical examination and analysis of serum lipid levels.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1992
- Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1991
- Effects of three genetic loci in a pedigree with multiple lipoprotein phenotypes.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1991
- Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1991
- Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemiaThe American Journal of Cardiology, 1989
- Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred.Journal of Clinical Investigation, 1988
- The recognition and management of hyperlipidaemia in adults: A policy statement of the EuropeanEuropean Heart Journal, 1988
- Evidence That Men With Familial Hypercholesterolemia Can Avoid Early Coronary DeathPublished by American Medical Association (AMA) ,1986
- A comparison of positive family history definitions for defining risk of future diseaseJournal of Chronic Diseases, 1986