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Title
Key Questions About Familial Hypercholesterolemia
Authors
Keywords
-
Journal
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 79, Issue 10, Pages 1023-1031
Publisher
Elsevier BV
Online
2022-03-08
DOI
10.1016/j.jacc.2022.01.010
References
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Related references
Note: Only part of the references are listed.- Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries
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- Lipoprotein Metabolism in Familial Hypercholesterolemia
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- (2021) Marios Sagris et al. CARDIOVASCULAR RESEARCH
- Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland
- (2021) Eythór Björnsson et al. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
- Association of Monogenic vs Polygenic Hypercholesterolemia With Risk of Atherosclerotic Cardiovascular Disease
- (2020) Mark Trinder et al. JAMA Cardiology
- LPA genotype is associated with premature cardiovascular disease in familial hypercholesterolemia
- (2019) Martine Paquette et al. Journal of Clinical Lipidology
- Clinical utility of the polygenic LDL-C SNP score in familial hypercholesterolemia
- (2018) Marta Futema et al. ATHEROSCLEROSIS
- Clinical Genetic Testing for Familial Hypercholesterolemia
- (2018) Amy C. Sturm et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Impact of clinical signs and genetic diagnosis of familial hypercholesterolaemia on the prevalence of coronary artery disease in patients with severe hypercholesterolaemia
- (2017) Hayato Tada et al. EUROPEAN HEART JOURNAL
- Long-Term Risk of Atherosclerotic Cardiovascular Disease in US Adults With the Familial Hypercholesterolemia PhenotypeClinical Perspective
- (2016) Amanda M. Perak et al. CIRCULATION
- Premature coronary heart disease and autosomal dominant hypercholesterolemia: Increased risk in women with LDLR mutations
- (2016) Zahid Ahmad et al. Journal of Clinical Lipidology
- Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
- (2016) Amit V. Khera et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Genetic identification of familial hypercholesterolemia within a single U.S. health care system
- (2016) Noura S. Abul-Husn et al. SCIENCE
- Defining severe familial hypercholesterolaemia and the implications for clinical management: a consensus statement from the International Atherosclerosis Society Severe Familial Hypercholesterolemia Panel
- (2016) Raul D Santos et al. Lancet Diabetes & Endocrinology
- Severe heterozygous familial hypercholesterolemia and risk for cardiovascular disease: A study of a cohort of 14,000 mutation carriers
- (2014) Joost Besseling et al. ATHEROSCLEROSIS
- Lipoprotein(a) Levels in Familial Hypercholesterolemia
- (2014) Rodrigo Alonso et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Analysis of the frequency and spectrum of mutations recognised to cause familial hypercholesterolaemia in routine clinical practice in a UK specialist hospital lipid clinic
- (2013) Marta Futema et al. ATHEROSCLEROSIS
- 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
- Regulation of plasma LDL: the apoB paradigm
- (2009) Allan D. Sniderman et al. CLINICAL SCIENCE
- Familial-combined hyperlipidaemia in very young myocardial infarction survivors (
- (2009) F. Wiesbauer et al. EUROPEAN HEART JOURNAL
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