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Colesevelam added to combination therapy with a statin and ezetimibe in patients with familial hypercholesterolemia: A 12-week, multicenter, randomized, double-blind, controlled trial

Clinical therapeutics, 2010-04, Vol.32 (4), p.615-625

2010

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Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

The Lancet (British edition), 2012, Vol.379 (9822), p.1205-1213

2012

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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

Nature genetics, 2011-04, Vol.43 (4), p.339-344

2011

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Effect of aggressive versus conventional lipid lowering on atherosclerosis progression in familial hypercholesterolaemia (ASAP) : a prospective, randomised, double-blind trial

The Lancet (British edition), 2001-02, Vol.357 (9256), p.577-581

2001

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Antibody deficiency in patients with ataxia telangiectasia is caused by disturbed B- and T-cell homeostasis and reduced immune repertoire diversity

Journal of allergy and clinical immunology, 2013-05, Vol.131 (5), p.1367-1375.e9

2013

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ACAT inhibition and progression of carotid atherosclerosis in patients with familial hypercholesterolemia: the CAPTIVATE randomized trial

JAMA : the journal of the American Medical Association, 2009-03, Vol.301 (11), p.1131

2009

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Effectiveness of Inhibition of Cholesteryl Ester Transfer Protein by JTT-705 in Combination With Pravastatin in Type II Dyslipidemia

The American journal of cardiology, 2005-05, Vol.95 (9), p.1085-1088

2005

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The contribution of classical risk factors to cardiovascular disease in familial hypercholesterolaemia: data in 2400 patients

Journal of internal medicine, 2004-12, Vol.256 (6), p.482-490

2004

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Differential hs-CRP reduction in patients with familial hypercholesterolemia treated with aggressive or conventional statin therapy

Atherosclerosis, 2002-12, Vol.165 (2), p.361-366

2002

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Efficacy and Safety of Coadministration of Ezetimibe and Simvastatin in Adolescents With Heterozygous Familial Hypercholesterolemia

Journal of the American College of Cardiology, 2008-10, Vol.52 (17), p.1421-1429

2008

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Long term statin treatment reduces lipoprotein(a) concentrations in heterozygous familial hypercholesterolaemia

British heart journal, 2003-08, Vol.89 (8), p.893-896

2003

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Frequent mutation in the ABCC6 gene (R1141X) is associated with a strong increase in the prevalence of coronary artery disease

Circulation (New York, N.Y.), 2002-08, Vol.106 (7), p.773-775

2002

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Abnormalities in liver function and coagulation profile following the Fontan procedure

Heart (British Cardiac Society), 1999-07, Vol.82 (1), p.40-46

1999

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Long term survivors of childhood brain cancer have an increased risk for cardiovascular disease

Cancer, 2000-05, Vol.88 (9), p.2116-2121

2000

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Toll-like receptor-4 Asp299Gly polymorphism does not influence progression of atherosclerosis in patients with familial hypercholesterolaemia

European journal of clinical investigation, 2004-02, Vol.34 (2), p.94-99

2004

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Platelet Hyperreactivity and Prognosis in Survivors of Myocardial Infarction

The New England journal of medicine, 1990-05, Vol.322 (22), p.1549-1554

1990

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Incidence, predictability, and pathogenesis of amiodarone-induced thyrotoxicosis and hypothyroidism

The American journal of medicine, 1991-11, Vol.91 (5), p.507-511

1991

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Thrombospondin-2 polymorphism is associated with a reduced risk of premature myocardial infarction

Arteriosclerosis, thrombosis, and vascular biology, 2002-12, Vol.22 (12), p.e24

2002

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The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic disease

British journal of haematology, 1999-01, Vol.104 (1), p.50-54

1999

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Metabolic Syndrome and Risk of Coronary, Cerebral, and Peripheral Vascular Disease in a Large Dutch Population With Familial Hypercholesterolemia

Diabetes care, 2006-05, Vol.29 (5), p.1125-1127

2006

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Differences in intima-media thickness in the carotid and femoral arteries in familial hypercholesterolemic heterozygotes with and without clinical manifestations of cardiovascular disease

Atherosclerosis, 1999-10, Vol.146 (2), p.271-279

1999

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Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease

British journal of haematology, 1998-09, Vol.102 (5), p.1172-1175

1998

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Patients with premature coronary artery disease who carry the ABCC6 R1141X mutation have no Pseudoxanthoma Elasticum phenotype

International journal of cardiology, 2005-04, Vol.100 (3), p.389-393

2005

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Long term efficacy and safety of atorvastatin in the treatment of severe type III and combined dyslipidaemia

British heart journal, 2002-09, Vol.88 (3), p.234-238

2002

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The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosis

Atherosclerosis, 1998-11, Vol.141 (1), p.161-166

1998

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Colesevelam added to combination therapy with a statin and ezetimibe in patients with familial hypercholesterolemia: A 12-week, multicenter, randomized, double-blind, controlled trial

Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

Effect of aggressive versus conventional lipid lowering on atherosclerosis progression in familial hypercholesterolaemia (ASAP) : a prospective, randomised, double-blind trial

Antibody deficiency in patients with ataxia telangiectasia is caused by disturbed B- and T-cell homeostasis and reduced immune repertoire diversity

ACAT inhibition and progression of carotid atherosclerosis in patients with familial hypercholesterolemia: the CAPTIVATE randomized trial

Effectiveness of Inhibition of Cholesteryl Ester Transfer Protein by JTT-705 in Combination With Pravastatin in Type II Dyslipidemia

The contribution of classical risk factors to cardiovascular disease in familial hypercholesterolaemia: data in 2400 patients

Differential hs-CRP reduction in patients with familial hypercholesterolemia treated with aggressive or conventional statin therapy

Efficacy and Safety of Coadministration of Ezetimibe and Simvastatin in Adolescents With Heterozygous Familial Hypercholesterolemia

Long term statin treatment reduces lipoprotein(a) concentrations in heterozygous familial hypercholesterolaemia

Frequent mutation in the ABCC6 gene (R1141X) is associated with a strong increase in the prevalence of coronary artery disease

Abnormalities in liver function and coagulation profile following the Fontan procedure

Long term survivors of childhood brain cancer have an increased risk for cardiovascular disease

Toll-like receptor-4 Asp299Gly polymorphism does not influence progression of atherosclerosis in patients with familial hypercholesterolaemia

Platelet Hyperreactivity and Prognosis in Survivors of Myocardial Infarction

Incidence, predictability, and pathogenesis of amiodarone-induced thyrotoxicosis and hypothyroidism

Thrombospondin-2 polymorphism is associated with a reduced risk of premature myocardial infarction

The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic disease

Metabolic Syndrome and Risk of Coronary, Cerebral, and Peripheral Vascular Disease in a Large Dutch Population With Familial Hypercholesterolemia

Differences in intima-media thickness in the carotid and femoral arteries in familial hypercholesterolemic heterozygotes with and without clinical manifestations of cardiovascular disease

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease

Patients with premature coronary artery disease who carry the ABCC6 R1141X mutation have no Pseudoxanthoma Elasticum phenotype

Long term efficacy and safety of atorvastatin in the treatment of severe type III and combined dyslipidaemia

The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosis

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