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1. Prevalence and predictive role of hypertriglyceridemia in statin-treated patients at very high risk: Insights from the START study

3. rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography

5. Exome Sequencing in Suspected Monogenic Dyslipidemias

9. Prevalence and predictive role of hypertriglyceridemia in statin-treated patients at very high risk: insights from the START Study

17. Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study

31. A targeted apoB38.9 mutation in mice is associated with reduced hepatic cholesterol synthesis and enhanced lipid peroxidation

42. Lp(a): a genetic cause of clinical FH in children.

45. Erratum to: FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer’s disease

50. Prothrombotic gene variants as risk factors of acute myocardial infarction in young women

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