Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis.
The atrial natriuretic peptide genetic variant rs5068 is associated with a favorable cardiometabolic phenotype in a Mediterranean population.
A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemia.
Gelatinases and their tissue inhibitors in a group of subjects with metabolic syndrome.
Enhanced lipid peroxidation and platelet activation as potential contributors to increased cardiovascular risk in the low-HDL phenotype.
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy.
Nonalcoholic fatty liver and metabolic syndrome in Italy: results from a multicentric study of the Italian Arteriosclerosis society.
Protein oxidation in a group of subjects with metabolic syndrome.
Clinical utility of novel biomarkers for cardiovascular disease risk stratification.
Statin therapy in patients with aortic stenosis after the ASTRONOMER trial: is there still any space?
Prediction of incident type 2 diabetes mellitus based on a twenty-year follow-up of the Ventimiglia heart study.
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.
Evaluation of nitric oxide metabolites in a group of subjects with metabolic syndrome.
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women.
Lipase maturation factor 1 is required for endothelial lipase activity.
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia.
Searching for wheat plants with low toxicity in celiac disease: Between direct toxicity and immunologic activation.
The production of 85 kDa N-terminal fragment of apolipoprotein B in mutant HepG2 cells generated by targeted modification of apoB gene occurs by ALLN-inhibitable protease cleavage during translocation.
Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene.
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia.
Effects of PCSK9 variants on common carotid artery intima media thickness and relation to ApoE alleles.
A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain.
C-reactive protein but not soluble CD40 ligand and homocysteine is associated to common atherosclerotic risk factors in a cohort of coronary artery disease patients.
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia.
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia.
Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemia.
The metabolic syndrome predicts cardiovascular events in subjects with normal fasting glucose: results of a 15 years follow-up in a Mediterranean population.
Clinical symptoms in celiac patients on a gluten-free diet.
Molecular diagnosis of hypobetalipoproteinemia: an ENID review.
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography.
Decreased plasma soluble RAGE in patients with hypercholesterolemia: effects of statins.
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol.
Low-density lipoproteins generated during an oral fat load in mild hypertriglyceridemic and healthy subjects are smaller, denser, and have an increased low-density lipoprotein receptor binding affinity.
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues.
Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study.
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia.
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease.
Unexplained elevated serum pancreatic enzymes: a reason to suspect celiac disease.
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults.
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent.
Food intolerance and chronic constipation: manometry and histology study.
[Anti-TNF (infliximab) treatment in Crohn disease: safety profile].
Analysis of sterols by high-performance liquid chromatography/mass spectrometry combined with chemometrics.
Bovine seminal ribonuclease is cytotoxic for both malignant and normal telomerase-positive cells.
Family history, diabetes and extension of coronary atherosclerosis are strong predictors of adverse events after PTCA: A one-year follow-up study.
No association between the cystatin C gene polymorphism and Alzheimer's disease: a case-control study in an Italian population.
Cystatin C levels are decreased in acute myocardial infarction: effect of cystatin C G73A gene polymorphism on plasma levels.
Chronic constipation and food intolerance: a model of proctitis causing constipation.
A novel mutation of the DHCR7 gene in a sicilian compound heterozygote with Smith-Lemli-Opitz Syndrome.
Beta-2-glycoprotein I is growth regulated and plays a role as survival factor for hepatocytes.
Transient chylomicronemia preceding the onset of insulin-dependent diabetes in a young girl with no humoral markers of islet autoimmunity.
Differential apolipoprotein(a) isoform expression in heterozygosity is an independent contributor to lipoprotein(a) levels variability.
Lack of association between angiotensin converting enzyme polymorphism and sporadic Alzheimer's disease.
Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project.
Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction.
Oxidative status in nondiabetic middle-aged subjects with metabolic syndrome: preliminary data.
Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study.
Genetic variants of ANP and cardiometabolic protection: from populations to novel therapeutics.
A novel component of the metabolic syndrome: the oxidative stress.
Obesity and the metabolic syndrome in a student cohort from Southern Italy.
Hypertension and diabetes mellitus are associated with cardiovascular events in the elderly without cardiovascular disease. Results of a 15-year follow-up in a Mediterranean population.
Down regulation of CD11b and CD18 expression in children with hypercholesterolemia: a preliminary report.
Effect of the -420C/G variant of the resistin gene promoter on metabolic syndrome, obesity, myocardial infarction and kidney dysfunction.
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily.
The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarction.
Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second allele.
Low-density-lipoprotein peak particle size in a Mediterranean population.
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene.
Distribution of risk factors, plasma lipids, lipoproteins and dyslipidemias in a small Mediterranean island: the Ustica Project.
Factor VII activity is an independent predictor of cardiovascular mortality in elderly women of a Sicilian population: results of an 11-year follow-up.
Effectiveness of screening for known mutations in Sicilian patients with "probable" familial hypercholesterolemia.
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients.
Leukocyte count, diabetes mellitus and age are strong predictors of stroke in a rural population in southern Italy: an 8-year follow-up.
Prevalence of overweight and obesity in a rural southern Italy population and relationships with total and cardiovascular mortality: the Ventimiglia di Sicilia project.
Carotid atherosclerosis in hypercholesterolemic patients: relationship with cardiovascular events.
ApoE polymorphism in a small Mediterranean island: relationships with plasma lipids, lipoproteins and LDL particle size.
Lipoprotein(a) levels in relation to albumin concentration in childhood nephrotic syndrome.
Effects of Mediterranean diet on lipid levels and cardiovascular risk in renal transplant recipients.
Lipoprotein(A) levels and apoprotein(a) phenotypes in a Sicilian population.
Lipoprotein profile and high-density lipoproteins: subfractions distribution in centenarians.
Organ loci of catabolism of short truncations of apoB.
A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: genetic and metabolic studies.
HDL subfractions distribution in renal transplant recipients: lack of evidence of a reduction of HDL2 particles.
Familial hypobetalipoproteinemia is not associated with low levels of lipoprotein(a).
Apo-lipoprotein profile in subjects with extracranial carotid atherosclerosis.
[Plasma lipids and apoproteins. The effect of cigarette smoking]
Lipid and apoprotein behaviour after oral fat load in hypertriglyceridaemia.