Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217
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Title
Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217
Authors
Keywords
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Journal
EUROPEAN HEART JOURNAL
Volume 37, Issue 17, Pages 1384-1394
Publisher
Oxford University Press (OUP)
Online
2016-02-24
DOI
10.1093/eurheartj/ehw028
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Note: Only part of the references are listed.- Improving identification of familial hypercholesterolaemia in primary care: Derivation and validation of the familial hypercholesterolaemia case ascertainment tool (FAMCAT)
- (2015) Stephen F. Weng et al. ATHEROSCLEROSIS
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- Prevalence and treatment of familial hypercholesterolaemia in Australian communities
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- Canadian Cardiovascular Society Position Statement on Familial Hypercholesterolemia
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- Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society
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- Corrigendum
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- Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
- (2014) Ron Do et al. NATURE
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- (2013) B. G. Nordestgaard et al. EUROPEAN HEART JOURNAL
- Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation
- (2013) Gerald F. Watts et al. INTERNATIONAL JOURNAL OF CARDIOLOGY
- Discriminative Ability of LDL-Cholesterol to Identify Patients With Familial Hypercholesterolemia
- (2012) Roeland Huijgen et al. Circulation-Cardiovascular Genetics
- Cardiovascular risk in relation to functionality of sequence variants in the gene coding for the low-density lipoprotein receptor: a study among 29 365 individuals tested for 64 specific low-density lipoprotein-receptor sequence variants
- (2012) Roeland Huijgen et al. EUROPEAN HEART JOURNAL
- 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
- Familial hypercholesterolaemia: A model of care for Australasia
- (2011) Gerald F. Watts et al. ATHEROSCLEROSIS SUPPLEMENTS
- Harmonizing the Metabolic Syndrome
- (2009) K.G.M.M. Alberti et al. CIRCULATION
- The risk of tendon xanthomas in familial hypercholesterolaemia is influenced by variation in genes of the reverse cholesterol transport pathway and the low-density lipoprotein oxidation pathway
- (2009) D. M. Oosterveer et al. EUROPEAN HEART JOURNAL
- Comparison of Genetic Versus Clinical Diagnosis in Familial Hypercholesterolemia
- (2008) Fernando Civeira et al. AMERICAN JOURNAL OF CARDIOLOGY
- Genetically Elevated C-Reactive Protein and Ischemic Vascular Disease
- (2008) Jeppe Zacho et al. NEW ENGLAND JOURNAL OF MEDICINE
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