(Q24645376)

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Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study

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scholarly article

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Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study (English)

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hypercholesterolemia

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1 reference

based on heuristic

inferred from title

Stephen E Humphries

object named as

Steve E Humphries

8

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author name string

Andrew Neil

1

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Jackie Cooper

2

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John Betteridge

3

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Nigel Capps

4

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Ian McDowell

5

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Paul Durrington

6

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Mary Seed

7

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language of work or name

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publication date

November 2008

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European Heart Journal

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29

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21

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2625-33

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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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7 April 2017

Lovastatin-mediated G1 arrest is through inhibition of the proteasome, independent of hydroxymethyl glutaryl-CoA reductase

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7 April 2017

Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group

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7 April 2017

Simvastatin with or without ezetimibe in familial hypercholesterolemia

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

7 April 2017

Diagnosing familial hypercholesterolaemia: the relevance of genetic testing

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7 April 2017

Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

7 April 2017

Evaluation of methods for the measurement of low-density lipoprotein cholesterol.

1 reference

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7 April 2017

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

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7 April 2017

Lipid screening and cardiovascular health in childhood

1 reference

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27 September 2017

Genetic heterogeneity of autosomal dominant hypercholesterolemia.

1 reference

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27 September 2017

Statin treatment for children and adolescents with heterozygous familial hypercholesterolaemia: a systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

27 September 2017

Severe hypercholesterolemia in four British families with the D374Y mutation in the PCSK9 gene: long-term follow-up and treatment response

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

27 September 2017

Established and emerging coronary risk factors in patients with heterozygous familial hypercholesterolaemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

27 September 2017

Effect of aggressive versus conventional lipid lowering on atherosclerosis progression in familial hypercholesterolaemia (ASAP): a prospective, randomised, double-blind trial

1 reference

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27 September 2017

Extent of underdiagnosis of familial hypercholesterolaemia in routine practice: prospective registry study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

27 September 2017

Cohort study analysis with a FORTRAN computer program.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

27 September 2017

Heterozygous familial hypercholesterolemia. Relationship between plasma lipids, lipoproteins, clinical manifestations and ischaemic heart disease in men and women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

27 September 2017

Familial hypercholesterolemia in the Finnish north Karelia. A molecular, clinical, and genealogical study.

1 reference

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30 May 2018

Coronary artery disease in 116 kindred with familial type II hyperlipoproteinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

30 May 2018

Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

30 May 2018

Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

30 May 2018

Ischaemic disease in men and women with familial hypercholesterolaemia and xanthomatosis. A comparative study of genetic and environmental factors in 274 heterozygous cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

30 May 2018

Statins and cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

28 November 2018

Update and analysis of the University College London low density lipoprotein receptor familial hypercholesterolemia database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

28 November 2018

The PCSK9 gene R46L variant is associated with lower plasma lipid levels and cardiovascular risk in healthy U.K. men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

28 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

28 November 2018

Non-coronary heart disease mortality and risk of fatal cancer in patients with treated heterozygous familial hypercholesterolaemia: a prospective registry study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

28 November 2018

Molecular characterization of familial hypercholesterolemia in Spain: identification of 39 novel and 77 recurrent mutations in LDLR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

28 November 2018

Comparison of the risk of fatal coronary heart disease in treated xanthomatous and non-xanthomatous heterozygous familial hypercholesterolaemia: a prospective registry study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577142

28 November 2018

Risk of Fatal Stroke in Patients With Treated Familial Hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18840879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiovascular disease and mortality in statin-treated patients with familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18840879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family similarities in the age at coronary death in familial hypercholesterolaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18840879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hypercholesterolemia and apolipoprotein E4

1 reference

https://pubmed.ncbi.nlm.nih.gov/18840879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18840879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiovascular disease in familial hypercholesterolaemia: influence of low-density lipoprotein receptor mutation type and classic risk factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/18840879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/EURHEARTJ/EHN422

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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