| 2024 |
Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study |
Articolo in rivista |
Vai |
| 2024 |
Consensus document on diagnosis and management of familial hypercholesterolemia from the Italian Society for the Study of Atherosclerosis (SISA) |
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 |
| 2024 |
Erdheim-Chester disease as complex clinical presentation and diagnosis: A case report and concise review of literature |
Articolo in rivista |
Vai |
| 2024 |
Do genetically determined very high and very low LDL levels contribute to Lp(a) plasma concentration? |
Articolo in rivista |
Vai |
| 2023 |
Refinement of the diagnostic approach for the identification of children and adolescents affected by familial hypercholesterolemia: Evidence from the LIPIGEN study |
Articolo in rivista |
Vai |
| 2023 |
APOC-III: a Gatekeeper in Controlling Triglyceride Metabolism |
Review essay (rassegna critica) |
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 |
Lipoprotein(a) Genotype Influences the Clinical Diagnosis of Familial Hypercholesterolemia |
Articolo in rivista |
Vai |
| 2023 |
Novel LDL-cholesterol lowering therapies: A step forward a personalized medicine |
Nota o commento |
Vai |
| 2023 |
Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia |
Articolo in rivista |
Vai |
| 2022 |
Circulating Molecular Chaperones in Subjects with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: Data from the Zabùt Aging Project |
Articolo in rivista |
Vai |
| 2022 |
Lp(a): a genetic cause of clinical FH in children |
Nota o commento |
Vai |
| 2022 |
Efficacy and safety of lomitapide in familial chylomicronaemia syndrome |
Articolo in rivista |
Vai |
| 2022 |
A subgroup analysis of the ODYSSEY APPRISE study: Safety and efficacy of alirocumab in the Italian cohort |
Articolo in rivista |
Vai |
| 2022 |
Efficacy of Long-Term Treatment of Autosomal Recessive Hypercholesterolemia With Lomitapide: A Subanalysis of the Pan-European Lomitapide Study |
Articolo in rivista |
Vai |
| 2022 |
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study |
Articolo in rivista |
Vai |
| 2022 |
Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations |
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 |
Effects of PCSK9 inhibitors on HDL cholesterol efflux and serum cholesterol loading capacity in familial hypercholesterolemia subjects: a multi-lipid-center real-world evaluation |
Articolo in rivista |
Vai |
| 2022 |
Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients |
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 |
Hyperalphalipoproteinemia and Beyond: The Role of HDL in Cardiovascular Diseases |
Review essay (rassegna critica) |
Vai |
| 2021 |
Lipoprotein abnormalities in chronic kidney disease and renal transplantation |
Review essay (rassegna critica) |
Vai |
| 2021 |
Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome |
Articolo in rivista |
Vai |
| 2021 |
Lomitapide does not alter PCSK9 and Lp(a) levels in homozygous familial hypercholesterolemia patients: Analysis on cytokines and lipid profile |
Articolo in rivista |
Vai |
| 2021 |
Long-term efficacy of lipoprotein apheresis and lomitapide in the treatment of homozygous familial hypercholesterolemia (HoFH): a cross-national retrospective survey |
Articolo in rivista |
Vai |
| 2021 |
EFFICACY AND SAFETY OF LOMITAPIDE IN HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA: THE PAN-EUROPEAN RETROSPECTIVE OBSERVATIONAL STUDY |
Articolo in rivista |
Vai |
| 2021 |
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia |
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 |
| 2020 |
Genetically determined hypercholesterolaemia results into premature leucocyte telomere length shortening and reduced haematopoietic precursors |
Articolo in rivista |
Vai |
| 2020 |
Rapid degradation of ABCA1 protein following cAMP withdrawal and treatment with PKA inhibitor suggests ABCA1 is a short-lived protein primarily regulated at the transcriptional level |
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 |
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 |
NPC1L1 and ABCG5/8 induction explain synergistic fecal cholesterol excretion in ob/ob mice co-treated with PPAR-α and LXR agonists |
Articolo in rivista |
Vai |
| 2020 |
Therapeutic options for homozygous familial hypercholesterolemia: the role of Lomitapide |
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 |
Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics |
Articolo in rivista |
Vai |
| 2020 |
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features |
Articolo 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 |
| 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 |
| 2018 |
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred |
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 |
An unexplained congenital disorder of glycosylation-II in a child with neurohepatic involvement, hypercholesterolemia and hypoceruloplasminemia |
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 |
Lack of Correlation of Plasma HDL With Fecal Cholesterol and Plasma Cholesterol Efflux Capacity Suggests Importance of HDL Functionality in Attenuation of Atherosclerosis |
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 |
Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes |
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 |
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia |
Articolo in rivista |
Vai |
| 2017 |
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) |
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 |
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily |
Abstract in atti di convegno pubblicato 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 |
| 2016 |
Albumin versus solvent/detergent-treated pooled plasma as replacement fluid for long-term plasma exchange therapy in a patient with primary hypertriglyceridemia and recurrent hyperlipidemic pancreatitis |
Articolo in rivista |
Vai |
| 2016 |
Proprotein Convertase Subtilisin Kexin Type 9 Inhibition for Autosomal Recessive Hypercholesterolemia - Brief Report |
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 |
Individual analysis of patients with HoFH participating in a phase 3 trial with lomitapide: The Italian cohort |
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 |
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 |
| 2016 |
Lomitapide affects HDL composition and function |
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 |
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 |
Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up |
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 |
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia |
Articolo in rivista |
Vai |
| 2015 |
Exome sequencing in suspected monogenic dyslipidemias |
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 |
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature |
Articolo in rivista |
Vai |
| 2015 |
The pathophysiology of intestinal lipoprotein production |
Articolo in rivista |
Vai |
| 2014 |
Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk |
Articolo in rivista |
Vai |
| 2014 |
Lomitapide: a novel drug for homozygous familial hypercholesterolemia |
Articolo in rivista |
Vai |
| 2014 |
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE |
Proceedings |
Vai |
| 2014 |
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS |
Proceedings |
Vai |
| 2014 |
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH |
Proceedings |
Vai |
| 2014 |
eNOS activation by HDL is impaired in genetic CETP deficiency |
Articolo in rivista |
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 |
Metabolic mediators of the effects of body-mass index, overweight, and obesity on coronary heart disease and stroke: a pooled analysis of 97 prospective cohorts with 1·8 million participants |
Articolo in rivista |
Vai |
| 2013 |
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis |
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 |
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 |
Proceedings |
Vai |
| 2013 |
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. |
Articolo in rivista |
Vai |
| 2013 |
FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA |
Proceedings |
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 |
Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype |
Articolo in rivista |
Vai |
| 2012 |
Prothrombotic gene variants in AMI young women |
Proceedings |
Vai |
| 2012 |
Lipid and apoprotein composition of HDL in partial or complete CETP deficiency |
Articolo in rivista |
Vai |
| 2012 |
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia |
Proceedings |
Vai |
| 2012 |
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia |
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 |
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL |
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 |
| 2011 |
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia |
Articolo in rivista |
Vai |
| 2011 |
Identification of a novel mutation of MTP gene in a patient with abetalipoproteinemia. |
Articolo in rivista |
Vai |
| 2011 |
FUNCTIONAL EFFECT OF NOVEL AMINO ACID VARIANTS OF APOLIPOPROTEIN B IN FAMILIAL HYPOBETALIPOPROTEINEMIA |
Proceedings |
Vai |
| 2011 |
VASCULOPROTECTIVE FUNCTION OF HDL
FROM CETP-DEFICIENT SUBJECTS |
Proceedings |
Vai |
| 2011 |
PREVALENCE OF ANGPTL3 AND APOB
GENE MUTATIONS IN SUBJECTS WITH
COMBINED HYPOLIPIDEMIA |
Proceedings |
Vai |
| 2011 |
Metabolomic analysis of plasma from Alzheimer disease patients |
Proceedings |
Vai |
| 2011 |
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY |
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 |
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. |
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 |
A novel putative interactor for the low density
lipoprotein receptor cytoplasmic domain |
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 |
| 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 |
| 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 |
Food hypersensitivity as a cause of rectal bleeding in adults |
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 |
| 2008 |
A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia |
Proceedings |
Vai |
| 2008 |
Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient |
Articolo in rivista |
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 |
Association between plasma lipid levels and migraine in subjects aged > or =50 years: preliminary data from the Zabùt Aging Project |
Articolo in rivista |
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 |
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA |
Articolo in rivista |
Vai |
| 2007 |
Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins |
Articolo in rivista |
Vai |
| 2007 |
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (LDL)
receptor |
Proceedings |
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 |
IgA anti-actin antibodies ELISA in coeliac disease: A multicentre study. |
Articolo in rivista |
Vai |
| 2007 |
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. |
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 |
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL |
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 |
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. |
Articolo in rivista |
Vai |
| 2007 |
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA |
Articolo in rivista |
Vai |
| 2007 |
The PCSK9 gene: a new gene controlling cholesterolemia |
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 |
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 |
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS |
Proceedings |
Vai |
| 2006 |
CETP levels rather than polymorphisms as markers of coronary risk: healthy athlete with high HDL-C and coronary disease--effectiveness of probucol. |
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 |
VARIABLE PHENOTYPIC ESPRESSION IN A LIPID ABSORPTION DISORDER DUE TO A MOLECULAR DEFECT IN THE SARA2 GENE |
Proceedings |
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 |
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE |
Proceedings |
Vai |
| 2006 |
ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE LOW-HDL PHENOTYPE. |
Proceedings |
Vai |
| 2006 |
METALLOTHIONEIN 2A: A POSSIBLE CANDIDATE ABLE TO INTERACT WITH LDL-R CYTOPLASMIC TAIL |
Proceedings |
Vai |
| 2006 |
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA |
Proceedings |
Vai |
| 2006 |
A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE |
Proceedings |
Vai |
| 2006 |
Genetic heterogeneity of familial hypercholesterolemia in Sicily |
Proceedings |
Vai |
| 2006 |
THE METABOLIC SYNDROME PREDICTS CARDIOVASCULAR EVENTS IN SUBJECTS WITH NORMAL GLUCOSE TOLERANCE. A 15 YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION |
Proceedings |
Vai |
| 2006 |
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent |
Articolo in rivista |
Vai |
| 2006 |
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues |
Articolo in rivista |
Vai |
| 2006 |
Plasma calprotectin levels in patients suffering from acute pancreatitis. |
Articolo in rivista |
Vai |
| 2006 |
Terapia biologica con infliximab (anti-TNF) nella malattia di Crohn: analisi delle complicanze. |
Articolo in rivista |
Vai |
| 2006 |
Additive effect of mutations in LDLR and PCSK9 genes on the phenotyoe of familial hypercholesterolemia |
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 |
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA |
Proceedings |
Vai |
| 2005 |
ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE “LOW-HDL” PHENOTYPE. |
Proceedings |
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 |
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia. |
Articolo in rivista |
Vai |
| 2005 |
Diabetes, family hystory and extension of coronary atherosclerosis are strong predictors of adverse events after PTCA: a one year follow-up study |
Articolo in rivista |
Vai |
| 2005 |
MUSCLE DAMAGE AND PAIN IN HYPERCHOLESTEROLEMIC OUT-PATIENTS POPULATION ON STATIN TREATMENT. |
Proceedings |
Vai |
| 2005 |
FAMILIAL HYPOALPHALIPOPROTEINEMIA ASSOCIATED TO CORNEAL OPACITIES IN ABSENCE OF LCAT DEFICIENCY |
Proceedings |
Vai |
| 2005 |
DIFFERENCE IN THE PREVALENCE OF METABOLIC SYNDROME AND CARDIOVASCULAR RISK FACTORS AFTER 14 YEARS IN THE POPULATION OF VENTIMIGLIA DI SICILIA |
Proceedings |
Vai |
| 2005 |
ADDITIVE EFFECT OF MUTATIONS IN LDLR AND PCSK9 GENES ON THE PHENOTYPE OF FAMILIAL HYPERCHOLESTEROLEMIA. |
Proceedings |
Vai |
| 2005 |
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA |
Proceedings |
Vai |
| 2005 |
SEVERE MALABSORPTION AND DECREASED TRIGLYCERIDE RICH LIPOPROTEINS PRODUCTION IN A PROBAND CARRYING A MUTATION ENCODING FOR A TRUNCATED APOLIPOPROTEIN B100 VARIANT (APO B 34.8). |
Proceedings |
Vai |
| 2005 |
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily |
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 |
| 2005 |
THE METABOLIC SYNDROME IS A PREDICTOR OF CARDIOVASCULAR EVENTS IN A SICILIAN POPULATION. RESULT OF A 15 YEARS FOLLOW UP |
Proceedings |
Vai |
| 2005 |
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT |
Proceedings |
Vai |
| 2005 |
HYPOALPHALIPOPROTEINEMIA ASSOCIATED TO CORNEAL OPACITIES IN ABSENCE OF LCAT DEFICIENCY. |
Proceedings |
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 |
| 2004 |
Transient chylomicronemic syndrome: description of three cases |
Abstract in rivista |
Vai |
| 2004 |
Increased risk for amnestic Mild Cognitive Impairment in subjects carrying the apolipoprotein e4 allele |
Proceedings |
Vai |
| 2004 |
NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS. |
Proceedings |
Vai |
| 2004 |
FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE |
Proceedings |
Vai |
| 2004 |
UNA NUOVA MUTAZIONE DELL’INTRONE 16 (G>A a 2390 -1) DEL RECETTORE DELLE LDL RESPONSABILE DI IPERCOLESTEROLEMIA FAMILIARE. EFFETTI SULLA ESPRESSIONE DELL’mRNA DEL RECETTORE DELLE LDL |
Proceedings |
Vai |
| 2004 |
FAMILIAL HDL DEFICIENCY DUE TO ABCA1 GENE MUTATIONS WITH OR WITHOUT OTHER GENETIC LIPOPROTEIN DISORDERS |
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 |
MUTAZIONI DEL GENE DELL’APOB RESPONSABILI DI IPOBETALIPOPROTEINEMIA FAMILIARE IN SICILIA |
Proceedings |
Vai |
| 2004 |
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. |
Proceedings |
Vai |
| 2004 |
I livelli di cistatina C sono ridotti nell’infarto miocardico acuto. Effetto del polimorfismo G273A sui livelli plasmatici |
Abstract in rivista |
Vai |
| 2004 |
ASSOCIAZIONE DEL POLIMORFISMO Q192R DEL GENE DELLA PARAOXONASI I (PON1) CON LA MALATTIA CORONARICA IN UN CAMPIONE DI PZ CON INFARTO MIOCARDICO, MALATTIA CORONARICA NON INFARTUALE E SOGGETTI NORMALI. |
Proceedings |
Vai |
| 2004 |
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA |
Proceedings |
Vai |
| 2004 |
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY |
Proceedings |
Vai |
| 2004 |
No association of Cystatin C Polymorphism I in italian subjects with Alzheimer's disease |
Proceedings |
Vai |
| 2004 |
Transient chylomicronemia preceding the onset of insulin-dependent diabetes in a young girl with no humoral markers of islet autoimmunity. |
Articolo in rivista |
Vai |
| 2004 |
MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. |
Proceedings |
Vai |
| 2004 |
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. |
Proceedings |
Vai |
| 2004 |
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. |
Proceedings |
Vai |
| 2004 |
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING A MUTATION IN THE LDL-R GENE AND IN THE PCSK9 GENE |
Proceedings |
Vai |
| 2004 |
Lack of association of low density lipoprotein receptor-related protein gene exon 3 polymorphism in italian subjects with Alzheimer's disease |
Proceedings |
Vai |
| 2004 |
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects |
Proceedings |
Vai |
| 2004 |
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore |
Abstract in rivista |
Vai |
| 2003 |
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. |
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 |
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 |
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 |
No association between Glu298Asp endothelial nitric oxide synthase polymorphism and Italian sporadic Alzheimer's disease |
Articolo in rivista |
Vai |
| 2003 |
Saturated and unsaturated free fatty acids (FFA) modulate differently HDL uptake in hepatoma HEPG2 cells |
Abstract in rivista |
Vai |
| 2003 |
LDL size, density and receptor affinity variation during an oral load in mild hyper-triglyceridemic and normal subjects |
Abstract 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 |
Simvastatin reduces the levels of ApoE-containing triglyceride-rich lipoproteins in men with premature coronary artery disease |
Abstract in rivista |
Vai |
| 2002 |
Livelli di b-sitosterolo in una popolazione siciliana di pazienti ipercolesterolemici |
Abstract in rivista |
Vai |
| 2002 |
Descrizione di una famiglia siciliana con iper-alfa-lipoproteinemia con deficit di CETP |
Abstract in rivista |
Vai |
| 2002 |
Il polimorfismo genico del CD14 C(-260)>T non e’ un fattore di rischio per infarto miocardico acuto |
Abstract in rivista |
Vai |
| 2002 |
Variations in plasma lipids and in the LDL peak particle size after acute myocardial infarction |
Abstract in rivista |
Vai |
| 2002 |
Changes in levels of triglyceride-rich lipoprotein subfractions during dialysis in uremic patients |
Abstract in rivista |
Vai |
| 2002 |
Il polimorfismo genico CD14 C(-260)>T non e’ un fattore di rischio per infarto miocardico acuto |
Abstract in rivista |
Vai |
| 2002 |
CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction |
Proceedings |
Vai |
| 2002 |
Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project |
Articolo in rivista |
Vai |
| 2002 |
Levels of b-sitosterol in a sicilian sample of hyper-cholesterolemic patients |
Abstract in rivista |
Vai |
| 2002 |
Lack of association between angiotensin converting enzyme polymorphism and sporadic Alzheimer's disease |
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 |
| 2002 |
Studio epidemiologico “Ustica”: bassa prevalenza delle LDL aterogene in una popolazione mediterranea |
Abstract in rivista |
Vai |
| 2002 |
Bassa prevalenza delle LDL aterogene piccole e dense in una popolazione mediterranea |
Abstract 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 |
Description of a sicilian family with hyper-alpha-lipoproteinemia with deficit of CETP activity |
Abstract in rivista |
Vai |
| 2002 |
Bassa prevalenza delle LDL aterogene piccole e dense in una popolazione mediterranea |
Abstract in rivista |
Vai |
| 2002 |
CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction |
Proceedings |
Vai |
| 2002 |
Low prevalence of the atherogenic small, dense LDL in a mediterranean population. Nutrition, Metabolism and Cardiovascular Diseases |
Abstract in rivista |
Vai |
| 2001 |
Le variazioni dei valori dell’assetto lipidico durante la risposta di fase acuta post-infarto miocardico acuto sono accompagnate da modifiche nel size delle LDL |
Abstract 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 |
Carotid atherosclerosis in hypercholesterolemic patients: Relationship with cardiovascular events |
Articolo in rivista |
Vai |
| 2001 |
Determinants of enhanced thromboxane biosynthesis in renal transplantation |
Articolo in rivista |
Vai |
| 2001 |
Prevalenza di fattori di rischio e variazione temporale dei parametri lipidici in una serie consecutiva di 350 infarti acuti del miocardio registrati in una unita’ intensiva di Palermo. |
Abstract in rivista |
Vai |
| 2001 |
Effectiveness of screening for known mutations in Sicilian patients with "probable" familial hypercholesterolemia |
Articolo in rivista |
Vai |
| 2001 |
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients |
Articolo in rivista |
Vai |
| 2001 |
Chilomicronemia transitoria causa di diabete di tipo I in assenza di markers umorali di autoimmunità in una bambina di nove anni |
Abstract in rivista |
Vai |
| 2001 |
Variazioni delle sottofrazioni delle lipoproteine ricche in trigliceridi durante la dialisi in soggetti uremici |
Abstract 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 |
| 2000 |
Accumulo di VLDL/IDL contenenti ApoE in maschi normolipemici con cardiopatia ischemica precoce |
Abstract in rivista |
Vai |
| 2000 |
Descrizione di un modello minimo per lo studio della cinetica dei chilomicroni dopo pasto grasso |
Abstract in rivista |
Vai |
| 2000 |
Treatment of primary hypercholesterolemia: comparison of the effectiveness of different statins |
Abstract in rivista |
Vai |
| 2000 |
Accumulation of ApoE-containing triglyceride-rich lipoproteins in normolipidemic men with premature coronary artery disease |
Proceedings |
Vai |
| 1996 |
HDL subfractions distribution in renal transplant recipients: Lack of evidence of a reduction of HDL2 particles |
Articolo in rivista |
Vai |
| 1995 |
Plasma levels of lipoproteins and apolipoproteins in congenital hypothyroidism: effects of L-thyroxine substitution therapy |
Articolo in rivista |
Vai |
