(Q74449552)

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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

scientific article published on 01 January 1998

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10 November 2019

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 Group (English)

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10 November 2019

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author name string

X M Sun

1

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10 November 2019

D D Patel

2

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10 November 2019

B L Knight

3

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10 November 2019

A K Soutar

4

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10 November 2019

publication date

1 January 1998

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10 November 2019

Atherosclerosis

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10 November 2019

136

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10 November 2019

1

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10 November 2019

175-185

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10 November 2019

Molecular genetics of the LDL receptor gene in familial hypercholesterolemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Plasma mevalonic acid, an index of cholesterol synthesis in vivo, and responsiveness to HMG-CoA reductase inhibitors in familial hypercholesterolaemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Response to HMG CoA reductase inhibitors in heterozygous familial hypercholesterolemia due to the 10-kb deletion ("French Canadian mutation") of the LDL receptor gene

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Is responsiveness to lovastatin in familial hypercholesterolaemia heterozygotes influenced by the specific mutation in the low-density lipoprotein receptor gene?

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low-density-lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous familial hypercholesterolaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Deletion of exon 15 of the LDL receptor gene is associated with a mild form of familial hypercholesterolemia. FH-Espoo

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Phenotypic variation among familial hypercholesterolemics heterozygous for either one of two Afrikaner founder LDL receptor mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Determinants of lipid levels among children with heterozygous familial hypercholesterolemia in Norway.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Influence of apolipoprotein E genotypes on plasma lipid and lipoprotein concentrations: results from a segregation analysis in pedigrees with molecularly defined familial hypercholesterolemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defect.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

The LDL receptor gene: a mosaic of exons shared with different proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2897%2900181-0

7 January 2021

Identifiers

10.1016/S0021-9150(97)00181-0

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9544745%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9544745%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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