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

The Lancet (British edition), 2013-01, Vol.381 (9860), p.40-46

2013

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DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis

PloS one, 2021-03, Vol.16 (3), p.e0247402-e0247402

2021

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The role of registries in rare genetic lipid disorders: Review and introduction of the first global registry in lipoprotein lipase deficiency

Atherosclerosis, 2017-07, Vol.262, p.146-153

2017

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Withdrawal: Lipase maturation factor 1 is required for endothelial lipase activity

Journal of lipid research, 2019-09, Vol.60 (9), p.1641-1641

2019

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

European heart journal, 2023-04, Vol.44 (16), p.1429-1431

2023

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Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk

Current atherosclerosis reports, 2014-06, Vol.16 (6), p.414-414, Article 414

2014

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Nonalcoholic fatty liver and metabolic syndrome in Italy: results from a multicentric study of the Italian Arteriosclerosis society

Acta diabetologica, 2013-04, Vol.50 (2), p.241-249

2013

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

Journal of translational medicine, 2012-11, Vol.10 (1), p.235-235, Article 235

2012

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Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature

Atherosclerosis, 2015-03, Vol.239 (1), p.209-217

2015

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Diagnostic Accuracy of Fecal Calprotectin Assay in Distinguishing Organic Causes of Chronic Diarrhea from Irritable Bowel Syndrome: A Prospective Study in Adults and Children

Clinical chemistry (Baltimore, Md.), 2003-06, Vol.49 (6), p.861-867

2003

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Long-Term Efficacy and Safety of the Microsomal Triglyceride Transfer Protein Inhibitor Lomitapide in Patients With Homozygous Familial Hypercholesterolemia

Circulation (New York, N.Y.), 2017-07, Vol.136 (3), p.332-335

2017

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Lipase maturation factor 1 is required for endothelial lipase activity[S]

Journal of lipid research, 2011-06, Vol.52 (6), p.1162-1169

2011

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Threshold Effects of Circulating Angiopoietin-Like 3 Levels on Plasma Lipoproteins

The journal of clinical endocrinology and metabolism, 2017-09, Vol.102 (9), p.3340-3348

2017

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Anti-PCSK9 treatment: is ultra-low low-density lipoprotein cholesterol always good?

Cardiovascular research, 2018-10, Vol.114 (12), p.1595-1604

2018

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A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 2013-08, Vol.33 (8), p.2021

2013

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Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia

Arteriosclerosis, thrombosis, and vascular biology, 2012-03, Vol.32 (3), p.805

2012

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

Nutrition, metabolism, and cardiovascular diseases, 2021-05, Vol.31 (5), p.1542-1547

2021

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PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study

Atherosclerosis, 2020-01, Vol.292, p.209-214

2020

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Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model

Atherosclerosis, 2016-03, Vol.246, p.50-56

2016

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Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia

Arteriosclerosis, thrombosis, and vascular biology, 2015-12, Vol.35 (12), p.2694

2015

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The Atrial Natriuretic Peptide Genetic Variant rs5068 Is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population

Diabetes care, 2013-09, Vol.36 (9), p.2850-2856

2013

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Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia

Internal medicine journal, 2021-04, Vol.51 (4), p.585-590

2021

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Gelatinases and Their Tissue Inhibitors in a Group of Subjects With Metabolic Syndrome

Journal of investigative medicine, 2013-08, Vol.61 (6), p.978-983

2013

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Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins

Free radical biology & medicine, 2007-11, Vol.43 (9), p.1255-1262

2007

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The pathophysiology of intestinal lipoprotein production

Frontiers in physiology, 2015-03, Vol.6, p.61-61

2015

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

DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis

The role of registries in rare genetic lipid disorders: Review and introduction of the first global registry in lipoprotein lipase deficiency

Withdrawal: Lipase maturation factor 1 is required for endothelial lipase activity

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

Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk

Nonalcoholic fatty liver and metabolic syndrome in Italy: results from a multicentric study of the Italian Arteriosclerosis society

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

Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature

Diagnostic Accuracy of Fecal Calprotectin Assay in Distinguishing Organic Causes of Chronic Diarrhea from Irritable Bowel Syndrome: A Prospective Study in Adults and Children

Long-Term Efficacy and Safety of the Microsomal Triglyceride Transfer Protein Inhibitor Lomitapide in Patients With Homozygous Familial Hypercholesterolemia

Lipase maturation factor 1 is required for endothelial lipase activity[S]

Threshold Effects of Circulating Angiopoietin-Like 3 Levels on Plasma Lipoproteins

Anti-PCSK9 treatment: is ultra-low low-density lipoprotein cholesterol always good?

A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemia

Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia

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

PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study

Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model

Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia

The Atrial Natriuretic Peptide Genetic Variant rs5068 Is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population

Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia

Gelatinases and Their Tissue Inhibitors in a Group of Subjects With Metabolic Syndrome

Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins

The pathophysiology of intestinal lipoprotein production

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