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Common genetic variants do not associate with CAD in familial hypercholesterolemia.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 6, p. 809, doi. 10.1038/ejhg.2013.242
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- Publication type:
- Article
Improved access to life insurance after genetic diagnosis of familial hypercholesterolaemia: cross-sectional postal questionnaire study.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 7, p. 722, doi. 10.1038/ejhg.2012.5
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- Publication type:
- Article
PCSK9 inhibition: the way forward in the treatment of dyslipidemia.
- Published in:
- 2015
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- Publication type:
- journal article
Impact of statin therapy on coronary plaque composition: a systematic review and meta-analysis of virtual histology intravascular ultrasound studies.
- Published in:
- 2015
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- Publication type:
- journal article
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in the Netherlands.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 2, p. 116, doi. 10.1034/j.1399-0004.2000.570205.x
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- Publication type:
- Article
Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 297, doi. 10.1034/j.1399-0004.1999.560407.x
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- Publication type:
- Article
Physical activity modulates the effect of a lipoprotein lipase mutation (D9N) on plasma lipids and lipoproteins.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 2, p. 158, doi. 10.1034/j.1399-0004.1999.560212.x
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- Publication type:
- Article
The Asn9 variant of lipoprotein lipase is associated with the - 93G promoter mutation and an increased risk of coronary artery disease.
- Published in:
- Clinical Genetics, 1998, v. 53, n. 1, p. 27, doi. 10.1111/j.1399-0004.1998.tb02577.x
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- Publication type:
- Article