The different relations of PCSK9 and Lp(a) to the presence and severity of atherosclerotic lesions in patients with familial hypercholesterolemia
Author:
Funder
Capital Health Development Fund
CAMS Major Collaborative Innovation Project
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference43 articles.
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2. Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review;Austin;Am. J. Epidemiol.,2004
3. Low-density lipoprotein receptor gene mutations and cardiovascular risk in a large genetic cascade screening population;Umans-Eckenhausen;Circulation,2002
4. Ankle brachial index combined with Framingham Risk Score to predict cardiovascular events and mortality: a meta-analysis;Fowkes;JAMA.,2008
5. Peripheral arterial disease in heterozygous familial hypercholesterolemia;Pereira;Atherosclerosis,2015
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