The type of mutation in the low density lipoprotein receptor gene influences the cholesterol-lowering response of the HMG-CoA reductase inhibitor simvastatin in patients with heterozygous familial hypercholesterolaemia (Q28373582)

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English	The type of mutation in the low density lipoprotein receptor gene influences the cholesterol-lowering response of the HMG-CoA reductase inhibitor simvastatin in patients with heterozygous familial hypercholesterolaemia	scientific article

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The type of mutation in the low density lipoprotein receptor gene influences the cholesterol-lowering response of the HMG-CoA reductase inhibitor simvastatin in patients with heterozygous familial hypercholesterolaemia (English)

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hypercholesterolemia

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based on heuristic

inferred from title

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based on heuristic

inferred from title

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based on heuristic

inferred from title

Vilmundur Gudnason

object named as

V Gudnason

Vilmundur Gudnason

2

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object named as

Karen E Heath

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author name string

K E Heath

1

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S E Humphries

3

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M Seed

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Steve E Humphries

3

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Mary Seed

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language of work or name

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publication date

March 1999

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Atherosclerosis

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143

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41-54

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1

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Molecular genetics of the LDL receptor gene in familial hypercholesterolemia

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https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900274-3

7 January 2021

Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia.

1 reference

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A World Wide Web site for low-density lipoprotein receptor gene mutations in familial hypercholesterolemia: sequence-based, tabular, and direct submission data handling.

1 reference

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Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases

1 reference

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Influence of specific mutations at the LDL-receptor gene locus on the response to simvastatin therapy in Afrikaner patients with heterozygous familial hypercholesterolaemia

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Low-density lipoprotein receptor genotype-dependent response to cholesterol lowering by combined pravastatin and cholestyramine in familial hypercholesterolemia.

1 reference

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Similar response to simvastatin in patients heterozygous for familial hypercholesterolemia with mRNA negative and mRNA positive mutations

1 reference

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Influence of genotype at the low density lipoprotein (LDL) receptor gene locus on the clinical phenotype and response to lipid-lowering drug therapy in heterozygous familial hypercholesterolaemia. The Familial Hypercholesterolaemia Regression Study

1 reference

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Prevention of coronary heart disease in clinical practice: recommendations of the Task Force of the European Society of Cardiology, European Atherosclerosis Society and European Society of Hypertension

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

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Utilities for high throughput use of the single strand conformational polymorphism method: screening of 791 patients with familial hypercholesterolaemia for mutations in exon 3 of the low density lipoprotein receptor gene

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Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity

1 reference

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Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia

1 reference

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The effects of genotype and infant weight on adult plasma levels of fibrinogen, factor VII, and LDL cholesterol are additive

1 reference

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Identification of recurrent and novel mutations in exon 4 of the LDL receptor gene in patients with familial hypercholesterolemia in the United Kingdom.

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Familial Hypercholesterolaemia Regression Study: a randomised trial of low-density-lipoprotein apheresis.

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7 January 2021

Reduction of LDL cholesterol by 25% to 60% in patients with primary hypercholesterolemia by atorvastatin, a new HMG-CoA reductase inhibitor

1 reference

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Comparative dose efficacy study of atorvastatin versus simvastatin, pravastatin, lovastatin, and fluvastatin in patients with hypercholesterolemia (the CURVES study)

1 reference

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What targets should lipid-modulating therapy achieve to optimise the prevention of coronary heart disease?

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Statins do more than just lower cholesterol

1 reference

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APO E genotype and familial hypercholesterolaemia

1 reference

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The influence of apolipoprotein E phenotype on the response to lovastatin therapy in patients with heterozygous familial hypercholesterolemia

1 reference

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The response to lovastatin treatment in patients with heterozygous familial hypercholesterolemia is modulated by apolipoprotein E polymorphism

1 reference

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Evidence of non-deficient low-density lipoprotein receptor patients in a pool of subjects with clinical familial hypercholesterolemia profile

1 reference

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7 January 2021

Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394.

1 reference

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7 January 2021

Effect on plasma lipid levels of different classes of mutations in the low-density lipoprotein receptor gene in patients with familial hypercholesterolemia

1 reference

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Diagnosing familial hypercholesterolaemia in childhood by measuring serum cholesterol.

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Rising cholesterol levels in children with familial hypercholesterolaemia.

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Genetic testing for familial hypercholesterolaemia: practical and ethical issues

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7 January 2021

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10.1016/S0021-9150(98)00274-3

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