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Title
What is new in familial hypercholesterolemia?
Authors
Keywords
-
Journal
CURRENT OPINION IN LIPIDOLOGY
Volume 25, Issue 3, Pages 183-188
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2014-04-03
DOI
10.1097/mol.0000000000000073
References
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Related references
Note: Only part of the references are listed.- The effect of LDLR-negative genotype on CT coronary atherosclerosis in asymptomatic statin treated patients with heterozygous familial hypercholesterolemia
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- Low-density lipoprotein cholesterol reduction by inhibition of PCSK9
- (2013) Evan A. Stein CURRENT OPINION IN LIPIDOLOGY
- Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society
- (2013) B. G. Nordestgaard et al. EUROPEAN HEART JOURNAL
- The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia
- (2013) Jana Vandrovcova et al. GENETICS IN MEDICINE
- Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation
- (2013) Gerald F. Watts et al. INTERNATIONAL JOURNAL OF CARDIOLOGY
- Inheritance pattern of familial hypercholesterolemia and markers of cardiovascular risk
- (2013) D. Meeike Kusters et al. JOURNAL OF LIPID RESEARCH
- Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study
- (2013) Philippa J Talmud et al. LANCET
- Transfer of lipids to high-density lipoprotein (HDL) is altered in patients with familial hypercholesterolemia
- (2013) Lilton R.C. Martinez et al. METABOLISM-CLINICAL AND EXPERIMENTAL
- Cholesteryl Ester Transfer Protein Inhibitors in the Treatment of Dyslipidemia: A Systematic Review and Meta-Analysis
- (2013) Chuanwei Li et al. PLoS One
- Elevated PCSK9 Levels in Untreated Patients With Heterozygous or Homozygous Familial Hypercholesterolemia and the Response to High‐Dose Statin Therapy
- (2013) Frederick Raal et al. Journal of the American Heart Association
- Low-Density Lipoprotein Cholesterol–Lowering Effects of AMG 145, a Monoclonal Antibody to Proprotein Convertase Subtilisin/Kexin Type 9 Serine Protease in Patients With Heterozygous Familial Hypercholesterolemia
- (2012) Frederick Raal et al. CIRCULATION
- Apolipoprotein B Synthesis Inhibition With Mipomersen in Heterozygous Familial Hypercholesterolemia
- (2012) Evan A. Stein et al. CIRCULATION
- Reverse cholesterol transport in familial hypercholesterolemia
- (2012) Maryse Guerin CURRENT OPINION IN LIPIDOLOGY
- Familial Hypercholesterolemia in the Danish General Population: Prevalence, Coronary Artery Disease, and Cholesterol-Lowering Medication
- (2012) Marianne Benn et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Effect of a monoclonal antibody to PCSK9, REGN727/SAR236553, to reduce low-density lipoprotein cholesterol in patients with heterozygous familial hypercholesterolaemia on stable statin dose with or without ezetimibe therapy: a phase 2 randomised controlled trial
- (2012) Evan A Stein et al. LANCET
- Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study
- (2012) Marina Cuchel et al. LANCET
- The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: Study with artificial emulsions
- (2011) Marcia M. Carneiro et al. ATHEROSCLEROSIS
- Evaluation of subclinical atherosclerosis by computed tomography coronary angiography and its association with risk factors in familial hypercholesterolemia
- (2010) Marcio H. Miname et al. ATHEROSCLEROSIS
- Mipomersen, an apolipoprotein B synthesis inhibitor, for lowering of LDL cholesterol concentrations in patients with homozygous familial hypercholesterolaemia: a randomised, double-blind, placebo-controlled trial
- (2010) Frederick J Raal et al. LANCET
- Biological, clinical and population relevance of 95 loci for blood lipids
- (2010) Tanya M. Teslovich et al. NATURE
- Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project
- (2009) A Taylor et al. CLINICAL GENETICS
- Family tracing to identify patients with Familial Hypercholesterolaemia: the second Audit of the Department of Health Familial Hypercholesterolaemia Cascade Testing Project
- (2008) S G Hadfield et al. ANNALS OF CLINICAL BIOCHEMISTRY
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