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The Right Ventricle Explains Sex Differences in Survival in Idiopathic Pulmonary Arterial Hypertension

Chest, 2014-06, Vol.145 (6), p.1230-1236

2014

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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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Long-term safety and efficacy of high-dose atorvastatin treatment in patients with familial hypercholesterolemia

The American journal of cardiology, 2005-01, Vol.95 (2), p.264-266

2005

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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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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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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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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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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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Effect of atorvastatin (80 mg) and simvastatin (40 mg) on plasma fibrinogen levels and on carotid intima media thickness in patients with familial hypercholesterolemia

The American journal of cardiology, 2003-03, Vol.91 (5), p.604-606

2003

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A frequent mutation in the lipoprotein lipase gene (D9N) deteriorates the biochemical and clinical phenotype of familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 1999-11, Vol.19 (11), p.2708-2713

1999

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Regression of carotid and femoral artery intima-media thickness in familial hypercholesterolemia: treatment with simvastatin

Archives of internal medicine (1960), 2003-08, Vol.163 (15), p.1837

2003

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Two cases of amiodarone-induced thyrotoxicosis successfully treated with a short course of antithyroid drugs while amiodarone was continued

British Heart Journal, 1994-09, Vol.72 (3), p.266-268

1994

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An increase in plasma cholesterol independent of thyroid function during long-term amiodarone therapy. A dose-dependent relationship

Annals of internal medicine, 1991-01, Vol.114 (2), p.128-132

1991

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Uninhibited thyroidal uptake of radioiodine despite iodine excess in amiodarone-induced hypothyroidism

The journal of clinical endocrinology and metabolism, 1986-08, Vol.63 (2), p.485-491

1986

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Immunoradiometric assay of thyrotropin in plasma: its value in predicting response to thyroliberin stimulation and assessing thyroid function in amiodarone-treated patients

Clinical chemistry (Baltimore, Md.), 1986-03, Vol.32 (3), p.433-436

1986

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Detection of Myocardial Damage in Patients With Sarcoidosis

Circulation (New York, N.Y.), 2009-11, Vol.120 (20), p.1969-1977

2009

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The Right Ventricle Explains Sex Differences in Survival in Idiopathic Pulmonary Arterial Hypertension

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

Genetic variation at the phospholipid transfer protein locus affects its activity and high-density lipoprotein size and is a novel marker of cardiovascular disease susceptibility

Long-term safety and efficacy of high-dose atorvastatin treatment in patients with 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

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

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

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease

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

Effect of atorvastatin (80 mg) and simvastatin (40 mg) on plasma fibrinogen levels and on carotid intima media thickness in patients with familial hypercholesterolemia

A frequent mutation in the lipoprotein lipase gene (D9N) deteriorates the biochemical and clinical phenotype of familial hypercholesterolemia

Regression of carotid and femoral artery intima-media thickness in familial hypercholesterolemia: treatment with simvastatin

Two cases of amiodarone-induced thyrotoxicosis successfully treated with a short course of antithyroid drugs while amiodarone was continued

An increase in plasma cholesterol independent of thyroid function during long-term amiodarone therapy. A dose-dependent relationship

Uninhibited thyroidal uptake of radioiodine despite iodine excess in amiodarone-induced hypothyroidism

Immunoradiometric assay of thyrotropin in plasma: its value in predicting response to thyroliberin stimulation and assessing thyroid function in amiodarone-treated patients

Detection of Myocardial Damage in Patients With Sarcoidosis

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