(Q58007481)

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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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scholarly article

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academic journal article

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Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217 (English)

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coronary artery disease

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Familial hypercholesterolaemia

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arteriosclerotic heart disease

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low-density lipoprotein

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hypercholesterolemia

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object named as

Marianne Benn

1

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Anne Tybjærg-Hansen

3

object named as

Anne Tybjærg-Hansen

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Børge G. Nordestgaard

4

object named as

Børge G. Nordestgaard

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2

object named as

Gerald F. Watts

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language of work or name

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publication date

22 February 2016

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European Heart Journal

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37

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17

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1384-1394

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Familial hypercholesterolemia and coronary heart disease: a HuGE association review

1 reference

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21 January 2018

Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review

1 reference

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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

1 reference

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Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states

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Familial hypercholesterolemia in the danish general population: prevalence, coronary artery disease, and cholesterol-lowering medication.

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Prevalence and treatment of familial hypercholesterolaemia in Australian communities

1 reference

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Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation

1 reference

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Genetically elevated C-reactive protein and ischemic vascular disease

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2003 World Health Organization (WHO)/International Society of Hypertension (ISH) statement on management of hypertension

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Familial hypercholesterolaemia: a model of care for Australasia.

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Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics

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Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia.

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The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population.

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Comparison of the efficacy and safety of rosuvastatin versus atorvastatin, simvastatin, and pravastatin across doses (STELLAR* Trial).

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Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

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Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk

1 reference

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21 January 2018

Discriminative ability of LDL-cholesterol to identify patients with familial hypercholesterolemia: a cross-sectional study in 26,406 individuals tested for genetic FH.

1 reference

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21 January 2018

Comparison of genetic versus clinical diagnosis in familial hypercholesterolemia.

1 reference

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21 January 2018

Child-parent screening for familial hypercholesterolaemia: screening strategy based on a meta-analysis

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21 January 2018

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

1 reference

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21 January 2018

Canadian Cardiovascular Society position statement on familial hypercholesterolemia

1 reference

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21 January 2018

Family history and cardiovascular risk in familial hypercholesterolemia: data in more than 1000 children

1 reference

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21 January 2018

Coronary artery disease in 116 kindred with familial type II hyperlipoproteinemia

1 reference

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21 January 2018

Identifiers

10.1093/EURHEARTJ/EHW028

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Google Scholar paper ID

4615747617498082427

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PubMed publication ID

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2-s2.0-84966551189

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