| 2024 |
Do genetically determined very high and very low LDL levels contribute to Lp(a) plasma concentration? |
Articolo in rivista |
Vai |
| 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 |
| 2024 |
Erdheim-Chester disease as complex clinical presentation and diagnosis: A case report and concise review of literature |
Articolo in rivista |
Vai |
| 2024 |
Derivation and validation of a predictive mortality model of in-hospital patients with Acinetobacter baumannii nosocomial infection or colonization |
Articolo in rivista |
Vai |
| 2023 |
Diminishing benefits of urban living for children and adolescents' growth and development |
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 |
Statin-induced autoimmune myositis: a proposal of an "experience-based" diagnostic algorithm from the analysis of 69 patients |
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 |
Efficacy and safety of lomitapide in familial chylomicronaemia syndrome |
Articolo in rivista |
Vai |
| 2022 |
Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients |
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 |
| 2022 |
An unusual case of chronic diarrhea: a case report |
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 |
| 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 |
Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight |
Articolo in rivista |
Vai |
| 2021 |
Hyperalphalipoproteinemia and Beyond: The Role of HDL in Cardiovascular Diseases |
Review essay (rassegna critica) |
Vai |
| 2021 |
Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome |
Articolo in rivista |
Vai |
| 2021 |
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography |
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 |
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia |
Articolo in rivista |
Vai |
| 2021 |
Lipoprotein abnormalities in chronic kidney disease and renal transplantation |
Review essay (rassegna critica) |
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 |
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 |
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 |
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 |
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 |
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 |
REPOSITIONING OF THE GLOBAL EPICENTRE OF NON-OPTIMAL CHOLESTEROL |
Articolo in rivista |
Vai |
| 2020 |
Therapeutic options for homozygous familial hypercholesterolemia: the role of Lomitapide |
Articolo in rivista |
Vai |
| 2019 |
Polyvascular subclinical atherosclerosis in familial hypercholesterolemia: The role of cholesterol burden and gender |
Articolo 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 |
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 |
| 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 |
An irregular atrial tachycardia : What is the underlying mechanism? |
Recensione in rivista |
Vai |
| 2018 |
Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes |
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 |
| 2018 |
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred |
Articolo in rivista |
Vai |
| 2018 |
Anti-PCSK9 treatment: Is ultra-low LDL always good? |
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 |
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study |
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 |
| 2017 |
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) |
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 |
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study |
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 |
| 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 |
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 |
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily |
Abstract in atti di convegno pubblicato 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 |
| 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 |
A century of trends in adult human height |
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 |
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 |
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 |
PULMONARY EMBOLISM IN AN EMERGENCY CARE UNIT: EVALUATION OF PREDICTIVE FACTORS FROM CLINICAL HISTORY AND PHYSICAL EXAM |
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 |
A century of trends in adult human height |
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 |
Genetic epidemiology of ARH in Sicily |
Abstract in atti di convegno pubblicato 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 |
Characterization of a mutant form of human apolipoprotein B (Thr26-Tyr27del) associated with familial hypobetalipoproteinemia |
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 |
FISIOPATOLOGIA DELLA SINTESI DELLE LIPOPROTEINE INTESTINALI |
Articolo in rivista |
Vai |
| 2015 |
Exome sequencing in suspected monogenic dyslipidemias |
Articolo in rivista |
Vai |
| 2015 |
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia |
Articolo in rivista |
Vai |
| 2015 |
The pathophysiology of intestinal lipoprotein production |
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 |
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature |
Articolo in rivista |
Vai |
| 2015 |
Effects of Steatosis on Hepatic Hemodynamics in Patients with Metabolic Syndrome |
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 |
Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency |
Articolo in rivista |
Vai |
| 2014 |
Gelatinases and their tissue inhibitors in metabolic syndrome |
Proceedings |
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 |
Proceedings |
Vai |
| 2014 |
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE |
Proceedings |
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 |
Proceedings |
Vai |
| 2014 |
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS |
Proceedings |
Vai |
| 2014 |
Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk |
Articolo in rivista |
Vai |
| 2014 |
Oxidative status in metabolic syndrome |
Proceedings |
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 |
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 |
| 2013 |
CLINICAL CHARACTERISTICS AND PLASMA
LIPIDS IN SUBJECTS WITH FAMILIAL
COMBINED HYPOLIPIDEMIA:
A POOLED ANALYSIS |
Proceedings |
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 |
A NOVEL APOB MUTATION IDENTIFIED
BY EXOME SEQUENCING COSEGREGATES
WITH STEATOSIS, LIVER CANCER
AND HYPOCHOLESTEROLEMIA |
Proceedings |
Vai |
| 2013 |
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis |
Articolo in rivista |
Vai |
| 2013 |
LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C |
Proceedings |
Vai |
| 2013 |
Gelatinases and their tissue inhibitors in a group of subjects with metabolic syndrome |
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 |
Protein oxidation in a group of subjects with metabolic syndrome. |
Articolo in rivista |
Vai |
| 2013 |
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy |
Articolo in rivista |
Vai |
| 2012 |
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia |
Proceedings |
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 |
The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population |
Proceedings |
Vai |
| 2012 |
Statin therapy in patients with aortic stenosis after the ASTRONOMER trial: is there still any space? |
Articolo in rivista |
Vai |
| 2012 |
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia |
Articolo in rivista |
Vai |
| 2012 |
Clinical utility of novel biomarkers for cardiovascular disease risk stratification |
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 |
Proceedings |
Vai |
| 2012 |
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL |
Proceedings |
Vai |
| 2011 |
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY |
Articolo in rivista |
Vai |
| 2011 |
Searching for wheat plants with low toxicity in celiac disease: Between direct toxicity and immunologic activation. |
Articolo in rivista |
Vai |
| 2011 |
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY
ACIDS |
Proceedings |
Vai |
| 2011 |
Metabolomic analysis of plasma from Alzheimer disease patients |
Proceedings |
Vai |
| 2011 |
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia |
Articolo in rivista |
Vai |
| 2011 |
PREVALENCE OF ANGPTL3 AND APOB
GENE MUTATIONS IN SUBJECTS WITH
COMBINED HYPOLIPIDEMIA |
Proceedings |
Vai |
| 2010 |
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. |
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 |
| 2010 |
Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene |
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 |
A novel putative interactor for the low density
lipoprotein receptor cytoplasmic domain |
Articolo in rivista |
Vai |
| 2009 |
Effetti della dialisi sul rischio cardiovascolare nei pazienti uremici: aumento delle particelle remnants |
Capitolo o Saggio |
Vai |
| 2009 |
Down regulation of CD11b and CD18 expression in children with hypercholesterolemia: A preliminary report. |
Articolo in rivista |
Vai |
| 2009 |
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia |
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 |
Obesity and the metabolic syndrome in a student cohort from Southern Italy |
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 |
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 |
Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia |
Articolo in rivista |
Vai |
| 2008 |
A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia |
Proceedings |
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 |
| 2008 |
Clinical symptoms in celiac patients on a gluten-free diet. |
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 |
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL |
Proceedings |
Vai |
| 2007 |
Molecular diagnosis of hypobetalipoproteinemia: An ENID review |
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 |
GENETIC HETEROGENEITY OF SEVERE HYPOBETALIPOPROTEINEMIA |
Proceedings |
Vai |
| 2007 |
INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). |
Proceedings |
Vai |
| 2007 |
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? |
Proceedings |
Vai |
| 2007 |
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE |
Proceedings |
Vai |
| 2007 |
Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins |
Articolo in rivista |
Vai |
| 2007 |
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography |
Articolo in rivista |
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 |
Proceedings |
Vai |
| 2007 |
FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. |
Proceedings |
Vai |
| 2007 |
MUTATIONS IN THE CETP GENE IN ITALIAN SUBJECTS WITH HYPERALPHALIPOPROTEINEMIA |
Proceedings |
Vai |
| 2007 |
CARDIOVASCULAR RISK FACTORS ANALYSIS OF PEDIATRIC MATABOLIC SYNDROME |
Proceedings |
Vai |
| 2007 |
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY |
Proceedings |
Vai |
| 2007 |
THE METABOLIC SYNDROME PREDICTS CARDIOVASCULAR EVENTS IN SUBJECTS WITH NORMAL FASTING GLUCOSE. A FIFTEEN YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION |
Proceedings |
Vai |
| 2007 |
HYPERTENSION AND DIABETES MELLITUS PREDICT CARDIOVASCULAR EVENTS IN ELDERLY WITHOUT CARDIOVASCULARDISEASE. RESULTS OF FIFTEEN YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION. |
Proceedings |
Vai |
| 2007 |
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA |
Articolo in rivista |
Vai |
| 2006 |
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease |
Articolo in rivista |
Vai |
| 2006 |
Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study |
Articolo in rivista |
Vai |
| 2006 |
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS |
Proceedings |
Vai |
| 2006 |
Analysis of sterols by high-performance liquid chromatography/mass spectrometry combined with chemometrics |
Articolo in rivista |
Vai |
| 2006 |
Unexpleined elevated serum pancreatic enzymes: a reason to suspect celiac disease |
Articolo in rivista |
Vai |
| 2006 |
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults |
Articolo in rivista |
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. |
Proceedings |
Vai |
| 2006 |
Liver steatosis and metabolic syndrome: prevalence and correlation with metabolic parameters and ultrasonography evaluation of abdominal fat |
Proceedings |
Vai |
| 2006 |
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE |
Proceedings |
Vai |
| 2006 |
Genetic heterogeneity of familial hypercholesterolemia in Sicily |
Proceedings |
Vai |
| 2006 |
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent |
Articolo in rivista |
Vai |
| 2006 |
A Novel HPLC-MS Method for Analysis of Plasma Sterols |
Proceedings |
Vai |
| 2006 |
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues |
Articolo in rivista |
Vai |
| 2006 |
Terapia biologica con infliximab (anti-TNF) nella malattia di Crohn: analisi delle complicanze. |
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 |
| 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 |
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 |
Cystatin C levels are decreased in acute myocardial infarction: Effect of cystatin C G73A gene polymorphism on plasma levels |
Articolo in rivista |
Vai |
| 2005 |
Bovine seminal ribonuclease is cytotoxic for both malignant and normal telomerase-positive cells |
Articolo in rivista |
Vai |
| 2005 |
Chronic constipation and food intolerance: a model of proctitis causing constipation |
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 |
BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES |
Articolo in rivista |
Vai |
| 2004 |
LDL peak particle size and the extension of coronary atherosclerosis in 72 patients that underwent an angiographic exam |
Proceedings |
Vai |
| 2004 |
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY |
Proceedings |
Vai |
| 2003 |
Differential apolipoprotein(a) isoform expression in heterozygosity is an independent contributor to lipoprotein(a) levels variability |
Articolo in rivista |
Vai |
| 2003 |
Low-density-lipoprotein peak particle size in a Mediterranean population. |
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 |
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. |
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 |
Plasma calprotectin assay in patients with acute pancreatitis |
Proceedings |
Vai |
| 2003 |
Plasma calprotectin levels in patients suffering from acute pancreatitis |
Proceedings |
Vai |
| 2002 |
Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project |
Articolo in rivista |
Vai |
| 2002 |
Lack of association between angiotensin converting enzyme polymorphism and sporadic Alzheimer's disease |
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 |
| 2002 |
Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction |
Articolo in rivista |
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 |
| 2001 |
ApoE polymorphism in a small Mediterranean island: Relationships with plasma lipids, lipoproteins and LDL particle size |
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 |
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 |
| 2001 |
Carotid atherosclerosis in hypercholesterolemic patients: Relationship with cardiovascular events |
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 |
