The contribution of classical risk factors to cardiovascular disease in familial hypercholesterolaemia: data in 2400 patients
暂无分享,去创建一个
E. Sijbrands | M. Trip | J. Kastelein | A. Liem | M. Tanck | J. Kastelein | J. J. P. Kastelein | A. Jansen | P. Lansberg | H. W. O. Roeters van Lennep | A. C. M. Jansen | E. S. Aalst‐Cohen | M. W. Tanck | M. D. Trip | P. J. Lansberg | A. H. Liem | H. W. O. Roeters van Lennep | E. J. G. Sijbrands | H. W. R. Lennep | E. S. Aalst-Cohen | E. Aalst-Cohenvan
[1] J. Ferrières,et al. Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation. , 1995, Circulation.
[2] M. Schemper,et al. Predictive Accuracy and Explained Variation in Cox Regression , 2000, Biometrics.
[3] E. Boerwinkle,et al. Relation of serum lipoprotein(a) concentration and apolipoprotein(a) phenotype to coronary heart disease in patients with familial hypercholesterolemia. , 1990, The New England journal of medicine.
[4] R. Westendorp,et al. Additional risk factors influence excess mortality in heterozygous familial hypercholesterolaemia. , 2000, Atherosclerosis.
[5] Nicholas Smith,et al. Smoking Status and Risk for Recurrent Coronary Events after Myocardial Infarction , 2002, Annals of Internal Medicine.
[6] W. Riley,et al. Evaluation of coronary risk factors in patients with heterozygous familial hypercholesterolemia. , 2001, The American journal of cardiology.
[7] A. Zwinderman,et al. Efficacy and Safety of a Novel Cholesteryl Ester Transfer Protein Inhibitor, JTT-705, in Humans: A Randomized Phase II Dose-Response Study , 2002, Circulation.
[8] S. Kihara,et al. Characteristics of coronary artery disease and lipoprotein abnormalities in patients with heterozygous familial hypercholesterolemia associated with diabetes mellitus or impaired glucose tolerance. , 1997, Atherosclerosis.
[9] H. Hobbs,et al. Lipoprotein(a): intrigues and insights. , 1999, Current opinion in lipidology.
[10] F. Kronenberg,et al. Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defect. , 1996, Arteriosclerosis, thrombosis, and vascular biology.
[11] M. Hayden,et al. Genetic and environmental factors affecting the incidence of coronary artery disease in heterozygous familial hypercholesterolemia. , 1991, Arteriosclerosis and thrombosis : a journal of vascular biology.
[12] J. Danesh,et al. Lipoprotein(a) and Coronary Heart Disease: Meta-Analysis of Prospective Studies , 2000, Circulation.
[13] J. Kastelein,et al. The molecular basis of familial hypercholesterolemia in The Netherlands , 2001, Human Genetics.
[14] J. Kastelein,et al. Prevalence and significance of cardiovascular risk factors in a large cohort of patients with familial hypercholesterolaemia , 2003, Journal of internal medicine.
[15] J. Beaumont,et al. Ischaemic disease in men and women with familial hypercholesterolaemia and xanthomatosis. A comparative study of genetic and environmental factors in 274 heterozygous cases. , 1976, Atherosclerosis.
[16] J J Kastelein,et al. Mortality over two centuries in large pedigree with familial hypercholesterolaemia: family tree mortality study. , 2001, BMJ : British Medical Journal.
[17] B. Angelin,et al. Apolipoprotein(a) and ischaemic heart disease in familial hypercholesterolaemia , 1990, The Lancet.
[18] Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group. , 1991, BMJ.
[19] G. Boers,et al. Carotid and femoral artery wall thickness and stiffness in patients at risk for cardiovascular disease, with special emphasis on hyperhomocysteinemia. , 1998, Arteriosclerosis, thrombosis, and vascular biology.
[20] T. Miettinen,et al. Mortality and cholesterol metabolism in familial hypercholesterolemia. Long-term follow-up of 96 patients. , 1988, Arteriosclerosis.
[21] Uk-Prospective-Diabetes-Study-Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33) , 1998, The Lancet.
[22] Plasma Homocysteine as a Risk Factor for Vascular Disease , 1998 .
[23] T. Farag,et al. Familial hypercholesterolemia. , 1988, Journal of the Royal Society of Medicine.
[24] R. Holman,et al. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group. , 1998 .
[25] D B Rubin,et al. Multiple imputation in health-care databases: an overview and some applications. , 1991, Statistics in medicine.
[26] E. Boerwinkle,et al. Apolipoprotein(a) gene accounts for greater than 90% of the variation in plasma lipoprotein(a) concentrations. , 1992, The Journal of clinical investigation.
[27] Per Magne Ueland,et al. Homocysteine and risk of ischemic heart disease and stroke: a meta-analysis. , 2002, JAMA.
[28] J. Witteman,et al. Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action Project. , 1997, JAMA.