Cardiovascular disease in familial hypercholesterolaemia: Influence of low-density lipoprotein receptor mutation type and classic risk factors

This publication has 31 references indexed in Scilit:

• Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk
  Journal of Medical Genetics, 2006
• Monounsaturated Fat and Cardiovascular Risk
  2006
• Diagnosing familial hypercholesterolaemia: the relevance of genetic testing
  European Heart Journal, 2006
• Influence of HDL Cholesterol on Preclinical Carotid Atherosclerosis in Familial Hypercholesterolemia
  Arteriosclerosis, Thrombosis, and Vascular Biology, 2006
• Established and emerging coronary risk factors in patients with heterozygous familial hypercholesterolaemia
  Heart, 2004
• Cascade genetic screening for familial hypercholesterolemia
  Clinical Genetics, 2004
• Apolipoprotein E genotype is not associated with cardiovascular disease in heterozygous subjects with familial hypercholesterolemia
  American Heart Journal, 2003
• Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III)
  JAMA, 2001
• Importance of HDL cholesterol levels and the total/ HDL cholesterol ratio as a risk factor for coronary heart disease in molecularly defined heterozygous familial hypercholesterolaemia
  European Heart Journal, 2001
• Universal primer quantitative fluorescent multiplex (UPQFM) PCR: a method to detect major and minor rearrangements of the low density lipoprotein receptor gene
  Journal of Medical Genetics, 2000