Comparison of Genetic Versus Clinical Diagnosis in Familial Hypercholesterolemia
- 1 November 2008
- journal article
- research article
- Published by Elsevier BV in The American Journal of Cardiology
- Vol. 102 (9), 1187-1193.e1
- https://doi.org/10.1016/j.amjcard.2008.06.056
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Femoral Atherosclerosis In Heterozygous Familial HypercholesterolemiaArteriosclerosis, Thrombosis, and Vascular Biology, 2008
- Diagnosing familial hypercholesterolaemia: the relevance of genetic testingEuropean Heart Journal, 2006
- Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease riskJournal of Medical Genetics, 2006
- Genetic screening protocol for familial hypercholesterolemia which includes splicing defects gives an improved mutation detection rateAtherosclerosis, 2005
- The Use of Achilles Tendon Sonography to Distinguish Familial Hypercholesterolemia from Other Genetic DyslipidemiasArteriosclerosis, Thrombosis, and Vascular Biology, 2005
- Tendon Xanthomas in Familial Hypercholesterolemia Are Associated With Cardiovascular Risk Independently of the Low-Density Lipoprotein Receptor Gene MutationArteriosclerosis, Thrombosis, and Vascular Biology, 2005
- A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemiaAtherosclerosis, 2003
- Mutations in PCSK9 cause autosomal dominant hypercholesterolemiaNature Genetics, 2003
- Impact of genetic defects on atherosclerosis in patients suspected of familial hypercholesterolaemiaEuropean Journal of Clinical Investigation, 2001
- Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular geneticsThe American Journal of Cardiology, 1993