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Pubblicazioni

Data Titolo Tipologia Scheda
2024 Worldwide trends in underweight and obesity from 1990 to 2022: a pooled analysis of 3663 population-representative studies with 222 million children, adolescents, and adults Articolo in rivista Vai
2023 Statin-induced autoimmune myositis: a proposal of an "experience-based" diagnostic algorithm from the analysis of 69 patients Articolo in rivista Vai
2023 Consensus document on Lipoprotein(a) from the Italian Society for the Study of Atherosclerosis (SISA) Articolo in rivista Vai
2023 Diminishing benefits of urban living for children and adolescents' growth and development Articolo in rivista Vai
2023 Global variation in diabetes diagnosis and prevalence based on fasting glucose and hemoglobin A1c Articolo in rivista Vai
2022 Colon cancer in a 12-year-old girl with hypertriglyceridemia Articolo in rivista Vai
2022 Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients Articolo in rivista Vai
2022 Efficacy and safety of lomitapide in familial chylomicronaemia syndrome Articolo in rivista Vai
2022 Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects: Polygenic hypocholesterolemias Articolo in rivista Vai
2022 An unusual case of chronic diarrhea: a case report Articolo in rivista Vai
2022 Lifestyle versus ezetimibe plus lifestyle in patients with biopsy-proven non-alcoholic steatohepatitis (LISTEN): A double-blind randomised placebo-controlled trial Articolo in rivista Vai
2021 Lipoprotein abnormalities in chronic kidney disease and renal transplantation Review essay (rassegna critica) Vai
2021 Hyperalphalipoproteinemia and Beyond: The Role of HDL in Cardiovascular Diseases Review essay (rassegna critica) Vai
2021 rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography Articolo in rivista Vai
2021 Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight Articolo in rivista Vai
2021 Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants Articolo in rivista Vai
2021 EFFECTIVENESS AND SAFETY OF LOMITAPIDE IN A PATIENT WITH FAMILIAL CHYLOMICRONEMIA SYNDROME Abstract in atti di convegno pubblicato in rivista Vai
2021 DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis Articolo in rivista Vai
2021 Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia Articolo in rivista Vai
2020 PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study Articolo in rivista Vai
2020 Therapeutic options for homozygous familial hypercholesterolemia: the role of Lomitapide Articolo in rivista Vai
2020 National Trends in Total Cholesterol Obscure Heterogeneous Changes in HDL and non-HDL Cholesterol and total-to-HDL Cholesterol Ratio: A Pooled Analysis of 458 Population-Based Studies in Asian and Western Countries Articolo in rivista Vai
2020 Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics Articolo in rivista Vai
2020 REPOSITIONING OF THE GLOBAL EPICENTRE OF NON-OPTIMAL CHOLESTEROL Articolo in rivista Vai
2020 HEIGHT AND BODY-MASS INDEX TRAJECTORIES OF SCHOOL-AGED CHILDREN AND ADOLESCENTS FROM 1985 TO 2019 IN 200 COUNTRIES AND TERRITORIES: A POOLED ANALYSIS OF 2181 POPULATION-BASED STUDIES WITH 65 MILLION PARTICIPANTS. Articolo in rivista Vai
2020 PCSK9-D374Y MEDIATED LDL-R DEGRADATION CAN BE FUNCTIONALLY INHIBITED BY EGF-A AND TRUNCATED EGF-A PEPTIDES. AN IN VITRO STUDY Abstract in atti di convegno pubblicato in rivista Vai
2020 MUTATION IN CANDIDATE GENES ACCOUNT FOR A SMALL MINORITY OF HYPOBETALIPOPROTEINEMIAS AND NGS ANALYSIS SUPPORT POLYGENICITY IN MUTATION-NEGATIVE PATIENTS Abstract in atti di convegno pubblicato in rivista Vai
2020 MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" Abstract in atti di convegno pubblicato in rivista Vai
2020 Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome Articolo in rivista Vai
2019 Relationship of a Body Shape Index and Body Roundness Index with carotid atherosclerosis in arterial hypertension Articolo in rivista Vai
2019 Resting energy expenditure and substrate oxidation in malnourished patients with type 1 glycogenosis Articolo in rivista Vai
2019 PREVALENCE OF STATIN INTOLERANCE IN A COHORT OF OUTPATIENTS IN A LIPID CLINIC Abstract in atti di convegno pubblicato in rivista Vai
2019 IDENTIFICATION OF P.LEU167DEL APOE GENE MUTATION BY NEXT GENERATION SEQUENCING IN A LARGE HYPERCHOLESTEROLEMIC FAMILY Abstract in atti di convegno pubblicato in rivista Vai
2019 Polyvascular subclinical atherosclerosis in familial hypercholesterolemia: The role of cholesterol burden and gender Articolo in rivista Vai
2018 An irregular atrial tachycardia : What is the underlying mechanism? Recensione in rivista Vai
2018 Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred Articolo in rivista Vai
2018 Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes Articolo in rivista Vai
2018 Lipoprotein-associated phospholipase A2 activity is increased in patients with definite familial hypercholesterolemia compared with other forms of hypercholesterolemia Articolo in rivista Vai
2018 Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study Articolo in rivista Vai
2018 Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score” Articolo in rivista Vai
2018 Anti-PCSK9 treatment: Is ultra-low LDL always good? Articolo in rivista Vai
2018 Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score Articolo in rivista Vai
2018 Contributions of mean and shape of blood pressure distribution to worldwide trends and variations in raised blood pressure: a pooled analysis of 1018 population-based measurement studies with 88.6 million participants Articolo in rivista Vai
2017 Association between familial hypobetalipoproteinemia and the risk of diabetes. Is this the other side of the cholesterol–diabetes connection? A systematic review of literature Articolo in rivista Vai
2017 Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing Articolo in rivista Vai
2017 Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia Articolo in rivista Vai
2017 Efficacy of Lomitapide in the Treatment of Familial Homozygous Hypercholesterolemia: Results of a Real-World Clinical Experience in Italy Articolo in rivista Vai
2017 Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily Abstract in atti di convegno pubblicato in rivista Vai
2017 Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) Articolo in rivista Vai
2017 Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study Articolo in rivista Vai
2017 Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults Articolo in rivista Vai
2017 Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19.1 million participants Articolo in rivista Vai
2017 Atorvastatin but not pravastatin impairs mitochondrial function in human pancreatic islets and rat β-cells. Direct effect of oxidative stress Articolo in rivista Vai
2016 FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease Articolo in rivista Vai
2016 Characterization of a mutant form of human apolipoprotein B (Thr26-Tyr27del) associated with familial hypobetalipoproteinemia Articolo in rivista Vai
2016 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 Articolo in rivista Vai
2016 Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population Articolo in rivista Vai
2016 Worldwide trends in diabetes since 1980: A pooled analysis of 751 population-based studies with 4.4 million participants Articolo in rivista Vai
2016 Trends in Adult Body-Mass Index in 200 Countries From 1975 to 2014: A Pooled Analysis of 1698 Population-Based Measurement Studies With 19·2 Million Participants Articolo in rivista Vai
2016 Metabolic disturbances and risk of cancer in the 25 years follow-up of the “Ventimiglia Heart Study” epidemiological project Abstract in atti di convegno pubblicato in rivista Vai
2016 A century of trends in adult human height Articolo in rivista Vai
2016 A century of trends in adult human height Articolo in rivista Vai
2016 PULMONARY EMBOLISM IN AN EMERGENCY CARE UNIT: EVALUATION OF PREDICTIVE FACTORS FROM CLINICAL HISTORY AND PHYSICAL EXAM Articolo in rivista Vai
2016 Erratum: FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease (Analytical and Bioanalytical Chemistry DOI: 10.1007/s00216-015-9229-6) Articolo in rivista Vai
2016 Genetic epidemiology of ARH in Sicily Abstract in atti di convegno pubblicato in rivista Vai
2015 Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature Articolo in rivista Vai
2015 FISIOPATOLOGIA DELLA SINTESI DELLE LIPOPROTEINE INTESTINALI Articolo in rivista Vai
2015 Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency Articolo in rivista Vai
2015 Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients. Articolo in rivista Vai
2015 Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia Articolo in rivista Vai
2015 Effects of Steatosis on Hepatic Hemodynamics in Patients with Metabolic Syndrome Articolo in rivista Vai
2015 Role of Nutraceuticals in Hypolipidemic Therapy Articolo in rivista Vai
2015 Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia Articolo in rivista Vai
2015 The pathophysiology of intestinal lipoprotein production Articolo in rivista Vai
2015 Effects of diabetes definition on global surveillance of diabetes prevalence and diagnosis: A pooled analysis of 96 population-based studies with 331 288 participants Articolo in rivista Vai
2015 Exome sequencing in suspected monogenic dyslipidemias Articolo in rivista Vai
2014 RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE eedings Vai
2014 LA LIPIDOMICA DELLA NON ALCOHOLIC FATTY LIVER DISEASE: ANALISI DELLA CINETICA DELL’ACIDO PALMITICO MEDIANTE L’USO DI UN ISOTOPO STABILE IN UN MODELLO IN VITRO eedings Vai
2014 NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS eedings Vai
2014 Gelatinases and their tissue inhibitors in metabolic syndrome eedings Vai
2014 Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk Articolo in rivista Vai
2014 Lipid Peroxidation, Nitric Oxide Metabolites, and Their Ratio in a Group of Subjects with Metabolic Syndrome Articolo in rivista Vai
2014 DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH eedings Vai
2014 Oxidative status in metabolic syndrome eedings Vai
2013 A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA eedings Vai
2013 LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C eedings Vai
2013 CLINICAL CHARACTERISTICS AND PLASMA LIPIDS IN SUBJECTS WITH FAMILIAL COMBINED HYPOLIPIDEMIA: A POOLED ANALYSIS eedings Vai
2013 Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype Articolo in rivista Vai
2013 The Atrial Natriuretic Peptide Genetic Variant Rs5068 Is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population Articolo in rivista Vai
2013 Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study Articolo in rivista Vai
2013 Nonalcoholic fatty liver and metabolic syndrome in Italy: Results from a multicentric study of the Italian Arteriosclerosis society Articolo in rivista Vai
2013 Protein oxidation in a group of subjects with metabolic syndrome. Articolo in rivista Vai
2013 Gelatinases and their tissue inhibitors in a group of subjects with metabolic syndrome Articolo in rivista Vai
2013 Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis Articolo in rivista Vai
2013 Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy Articolo in rivista Vai
2013 A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. Articolo in rivista Vai
2013 Oxidative status in nondiabetic middle-aged subjects with metabolic syndrome: preliminary data. Articolo in rivista Vai
2012 Statin therapy in patients with aortic stenosis after the ASTRONOMER trial: is there still any space? Articolo in rivista Vai
2012 Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL eedings Vai
2012 Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia eedings Vai
2012 Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia Articolo in rivista Vai
2012 Evaluation of nitric oxide metabolites in a group of subjects with metabolic syndrome. Articolo in rivista Vai
2012 Prothrombotic gene variants in AMI young women eedings Vai
2012 The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population eedings Vai
2012 Prediction of incident type 2 diabetes mellitus based on a twenty-year follow-up of the Ventimiglia heart study Articolo in rivista Vai
2012 Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. Articolo in rivista Vai
2012 Clinical utility of novel biomarkers for cardiovascular disease risk stratification Articolo in rivista Vai
2011 PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA eedings Vai
2011 LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS eedings Vai
2011 Searching for wheat plants with low toxicity in celiac disease: Between direct toxicity and immunologic activation. Articolo in rivista Vai
2011 Plasma non-cholesterol sterols in primary hypobetalipoproteinemia Articolo in rivista Vai
2011 LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY Articolo in rivista Vai
2011 Metabolomic analysis of plasma from Alzheimer disease patients eedings Vai
2010 A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain Articolo in rivista Vai
2010 Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. Articolo in rivista Vai
2010 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. Articolo in rivista Vai
2010 Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene Articolo in rivista Vai
2010 Effects of PCSK9 variants on common carotid artery intima media thickness and relation to ApoE alleles. Articolo in rivista Vai
2010 A novel component of the metabolic syndrome : The oxidative stress Articolo in rivista Vai
2009 Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia Articolo in rivista Vai
2009 Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. Articolo in rivista Vai
2009 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 Articolo in rivista Vai
2009 Effetti della dialisi sul rischio cardiovascolare nei pazienti uremici: aumento delle particelle remnants Capitolo o Saggio Vai
2009 Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia Articolo in rivista Vai
2009 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. Articolo in rivista Vai
2009 Obesity and the metabolic syndrome in a student cohort from Southern Italy Articolo in rivista Vai
2009 Down regulation of CD11b and CD18 expression in children with hypercholesterolemia: A preliminary report. Articolo in rivista Vai
2008 Clinical symptoms in celiac patients on a gluten-free diet. Articolo in rivista Vai
2008 A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia eedings Vai
2008 The metabolic syndrome predicts cardiovascular events in subjects with normal fasting glucose: Results of a 15 years follow-up in a Mediterranean population. Articolo in rivista Vai
2007 EFFECT OF THE 420C/G VARIANT OF THE RESISTIN GENE PROMOTER ON METABOLIC SYNDROME, OBESITY, MYOCARDIAL INFARCTION AND RENAL DYSFUNCTION Articolo in rivista Vai
2007 Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins Articolo in rivista Vai
2007 Molecular diagnosis of hypobetalipoproteinemia: An ENID review Articolo in rivista Vai
2007 CARDIOVASCULAR RISK FACTORS ANALYSIS OF PEDIATRIC MATABOLIC SYNDROME eedings Vai
2007 INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). eedings Vai
2007 MUTATIONS IN THE CETP GENE IN ITALIAN SUBJECTS WITH HYPERALPHALIPOPROTEINEMIA eedings Vai
2007 A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL eedings Vai
2007 ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? eedings Vai
2007 HYPERTENSION AND DIABETES MELLITUS PREDICT CARDIOVASCULAR EVENTS IN ELDERLY WITHOUT CARDIOVASCULARDISEASE. RESULTS OF FIFTEEN YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION. eedings Vai
2007 CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE eedings Vai
2007 GENETIC HETEROGENEITY OF SEVERE HYPOBETALIPOPROTEINEMIA eedings Vai
2007 TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA Articolo in rivista Vai
2007 FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. eedings Vai
2007 THE METABOLIC SYNDROME PREDICTS CARDIOVASCULAR EVENTS IN SUBJECTS WITH NORMAL FASTING GLUCOSE. A FIFTEEN YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION eedings Vai
2007 Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography Articolo in rivista Vai
2007 A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. Articolo in rivista Vai
2007 INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY eedings Vai
2007 SHORT APOB TRUNCATIONS SHOW IMPAIRE CHYLOMICRON EXPORT AND ENTEROCYTE TRIGLYCERIDE ACCUMULATION. IN VIVO AND IN VITRO EVIDENCE ON A APOB 28.25 STABLE-TRANSFECTED ENTEROCYTE CELL LINE eedings Vai
2006 Analysis of sterols by high-performance liquid chromatography/mass spectrometry combined with chemometrics Articolo in rivista Vai
2006 Liver steatosis and metabolic syndrome: prevalence and correlation with metabolic parameters and ultrasonography evaluation of abdominal fat eedings Vai
2006 Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study Articolo in rivista Vai
2006 CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE eedings Vai
2006 A Novel HPLC-MS Method for Analysis of Plasma Sterols eedings Vai
2006 A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS eedings Vai
2006 Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent Articolo in rivista Vai
2006 Genetic heterogeneity of familial hypercholesterolemia in Sicily eedings Vai
2006 COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. eedings Vai
2006 RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues Articolo in rivista Vai
2006 Multiple food hypersensitivity as a cause of refractory chronic constipation in adults Articolo in rivista Vai
2006 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. Articolo in rivista Vai
2006 Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease Articolo in rivista Vai
2006 Unexpleined elevated serum pancreatic enzymes: a reason to suspect celiac disease Articolo in rivista Vai
2006 Terapia biologica con infliximab (anti-TNF) nella malattia di Crohn: analisi delle complicanze. Articolo in rivista Vai
2005 Bovine seminal ribonuclease is cytotoxic for both malignant and normal telomerase-positive cells Articolo in rivista Vai
2005 No association between the cystatin C gene polymorphism and Alzheimer's disease: a case-control study in an Italian population. Articolo in rivista Vai
2005 Family hystory, diabetes and extension of coronary atherosclerosis are strong predictors of adverse events after PTCA: a one year follow-up study Articolo in rivista Vai
2005 Chronic constipation and food intolerance: a model of proctitis causing constipation Articolo in rivista Vai
2005 Cystatin C levels are decreased in acute myocardial infarction: Effect of cystatin C G73A gene polymorphism on plasma levels Articolo in rivista Vai
2005 A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome Articolo in rivista Vai
2004 LDL peak particle size and the extension of coronary atherosclerosis in 72 patients that underwent an angiographic exam eedings Vai
2004 HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY eedings Vai
2004 BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES Articolo in rivista Vai
2003 Plasma calprotectin assay in patients with acute pancreatitis eedings Vai
2003 Low-density-lipoprotein peak particle size in a Mediterranean population. Articolo in rivista Vai
2003 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 Articolo in rivista Vai
2003 Differential apolipoprotein(a) isoform expression in heterozygosity is an independent contributor to lipoprotein(a) levels variability Articolo in rivista Vai
2003 Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. Articolo in rivista Vai
2003 The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarction Articolo in rivista Vai
2003 Plasma calprotectin levels in patients suffering from acute pancreatitis eedings Vai
2002 Factor VII activity is an independent predictor of cardiovascular mortality in elderly women of a Sicilian population: Results of an 11-year follow-up Articolo in rivista Vai
2002 Lack of association between angiotensin converting enzyme polymorphism and sporadic Alzheimer's disease Articolo in rivista Vai
2002 Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project Articolo in rivista Vai
2002 Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction Articolo in rivista Vai
2002 Distribution of risk factors, plasma lipids, lipoproteins and dyslipidemias in a small Mediterranean island: the Ustica Project Articolo in rivista Vai
2001 Leukocyte count, diabetes mellitus and age are strong predictors of stroke in a rural population in southern Italy: An 8-year follow-up Articolo in rivista Vai
2001 Carotid atherosclerosis in hypercholesterolemic patients: Relationship with cardiovascular events Articolo in rivista Vai
2001 ApoE polymorphism in a small Mediterranean island: Relationships with plasma lipids, lipoproteins and LDL particle size Articolo in rivista Vai
2001 Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients Articolo in rivista Vai
2001 Prevalence of overweight and obesity in a rural southern Italy population and relationships with total and cardiovascular mortality: The Ventimiglia di Sicilia project Articolo in rivista Vai
1996 HDL subfractions distribution in renal transplant recipients: Lack of evidence of a reduction of HDL2 particles Articolo in rivista Vai