| 2024 |
Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study |
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 |
| 2024 |
Six genetic variants are associated with cardiovascular disease independently from canonical risk factors: a new method to refine GWAS results based on the UKBiobank phenotype database |
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 |
Consensus document on diagnosis and management of familial hypercholesterolemia 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 |
Novel LDL-cholesterol lowering therapies: A step forward a personalized medicine |
Nota o commento |
Vai |
| 2023 |
Lipoprotein(a) Genotype Influences the Clinical Diagnosis of Familial Hypercholesterolemia |
Articolo in rivista |
Vai |
| 2023 |
Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia |
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 |
APOC-III: a Gatekeeper in Controlling Triglyceride Metabolism |
Review essay (rassegna critica) |
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 |
| 2022 |
Clinical evaluation of bempedoic acid for the treatment of hyperlipidaemia |
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 |
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study |
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 |
| 2022 |
An unusual case of chronic diarrhea: a case report |
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 |
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 |
| 2021 |
Resistive index of ophthalmic artery as an imaging biomarker of hypertension-related vascular and
kidneydamage |
Articolo in rivista |
Vai |
| 2021 |
One year after the ESC/EAS guidelines on cholesterol control. What's the new evidence? What's missing? |
Review essay (rassegna critica) |
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 |
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 |
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography |
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 |
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 |
Practical guidance for combination lipid-modifying therapy in high- and very-high-risk patients: A statement from a European Atherosclerosis Society Task Force |
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 |
Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC) |
Articolo in rivista |
Vai |
| 2021 |
Resistive index of ophthalmic artery as an imaging biomarker of hypertension-related vascular and kidney damage |
Articolo in rivista |
Vai |
| 2021 |
Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome |
Articolo 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 |
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features |
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 |
Therapeutic options for homozygous familial hypercholesterolemia: the role of Lomitapide |
Articolo in rivista |
Vai |
| 2020 |
Rare dyslipidaemias, from phenotype to genotype to management: a European Atherosclerosis Society task force consensus statement |
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 |
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 |
Reported muscle symptoms during statin treatment amongst Italian dyslipidaemic patients in the real-life setting: the PROSISA Study |
Articolo in rivista |
Vai |
| 2020 |
Reported muscle symptoms during statin treatment amongst Italian dyslipidaemic patients in the real-life setting: the PROSISA Study |
Articolo in rivista |
Vai |
| 2020 |
Appropriateness criteria for the management of lipid-lowering therapy with alirocumab in high cardiovascular risk patients. The opinion of a multidisciplinary group of Italian experts |
Articolo 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 |
Genetically determined hypercholesterolaemia results into premature leucocyte telomere length shortening and reduced haematopoietic precursors |
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 |
Is echocardiography mandatory for patients with chronic kidney disease? |
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 |
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 |
Treatment effect of alirocumab according to age group, smoking status, and hypertension: Pooled analysis from 10 randomized ODYSSEY studies |
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 |
Statin utilization and lipid goal attainment in high or very-high cardiovascular risk patients: Insights from Italian general practice |
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 |
Major adverse cardiovascular events in non-valvular atrial fibrillation with chronic obstructive pulmonary disease: the ARAPACIS study |
Articolo in rivista |
Vai |
| 2018 |
Diabetes and aortic root dimension: A controversial subject |
Lettera |
Vai |
| 2018 |
Platelet Count Does Not Predict Bleeding in Cirrhotic Patients: Results from the PRO-LIVER Study |
Articolo in rivista |
Vai |
| 2018 |
Liver and statins: a critical appraisal of the evidence |
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 |
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 |
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 |
| 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 |
Differences in cardiac structure and function between black and white patients: Another step in the evaluation of cardiovascular risk in chronic kidney disease |
Nota o commento |
Vai |
| 2017 |
Inverse association between type 2 diabetes and aortic root dimension in hypertensive patients |
Articolo in rivista |
Vai |
| 2017 |
Severe reduction of blood lysosomal acid lipase activity in cryptogenic cirrhosis: A nationwide multicentre cohort study |
Articolo in rivista |
Vai |
| 2017 |
How to assess and manage cardiovascular risk associated with lipid alterations beyond LDL |
Articolo in rivista |
Vai |
| 2017 |
Threshold Effects of Circulating Angiopoietin-like 3 Levels on Plasma Lipoproteins |
Articolo in rivista |
Vai |
| 2017 |
Effect of aspirin on renal disease progression in patients with type 2 diabetes: A multicenter, double-blind, placebo-controlled, randomized trial. The renaL disEase progression by aspirin in diabetic pAtients (LEDA) trial. Rationale and study design |
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 |
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) |
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 |
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 |
Cardiovascular efficacy and safety of bococizumab in high-risk patients |
Articolo in rivista |
Vai |
| 2017 |
ANMCO/ISS/AMD/ANCE/ARCA/FADOI/GICR-IACPR/SICI-GISE/SIBioC/SIC/SICOA/SID/SIF/SIMEU/SIMG/SIMI/SISA Joint Consensus Document on cholesterol and cardiovascular risk: Diagnostic-therapeutic pathway in Italy |
Articolo in rivista |
Vai |
| 2017 |
Long-term efficacy and safety of the microsomal triglyceride transfer protein inhibitor lomitapide in patients with homozygous familial hypercholesterolemia |
Lettera |
Vai |
| 2017 |
The role of registries in rare genetic lipid disorders: Review and introduction of the first global registry in lipoprotein lipase deficiency |
Articolo in rivista |
Vai |
| 2017 |
Under-prescription of statins in patients with non-alcoholic fatty liver disease |
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 |
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily |
Abstract in atti di convegno pubblicato in rivista |
Vai |
| 2017 |
Diagnostic algorithm for familial chylomicronemia syndrome |
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 |
| 2016 |
Genetic susceptibility to the coronary artery diseases |
Capitolo o Saggio |
Vai |
| 2016 |
PULMONARY EMBOLISM IN AN EMERGENCY CARE UNIT: EVALUATION OF PREDICTIVE FACTORS FROM CLINICAL HISTORY AND PHYSICAL EXAM |
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 |
Efficacy and safety of adding alirocumab to rosuvastatin versus adding ezetimibe or doubling the rosuvastatin dose in high cardiovascular-risk patients: The ODYSSEY OPTIONS II randomized trial |
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 |
Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up |
Articolo in rivista |
Vai |
| 2016 |
Proprotein Convertase Subtilisin Kexin Type 9 Inhibition for Autosomal Recessive Hypercholesterolemia - Brief Report |
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 |
Lomitapide affects HDL composition and function |
Articolo in rivista |
Vai |
| 2016 |
Colesterolo e rischio cardiovascolare: Percorso diagnostico-terapeutico in Italia |
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 |
La diagnostica di laboratorio delle dislipidemie |
Articolo in rivista |
Vai |
| 2016 |
Documento di consenso intersocietario ANMCO/ISS/AMD/ANCE/ARCA/FADOI/ GICR-IACPR/SICI-GISE/SIBioC/SIC/SICOA/ SID/SIF/SIMEU/SIMG/SIMI/SISA Colesterolo e rischio cardiovascolare: percorso diagnostico-terapeutico in Italia |
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 |
Portal vein thrombosis relevance on liver cirrhosis: Italian Venous Thrombotic Events Registry |
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 |
| 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 |
Issues Affecting Quality of Life and Disease Burden in Lipoprotein Lipase Deficiency (Lpld) - First Step Towards a Pro Measure in Lpld |
Proceedings |
Vai |
| 2015 |
Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients. |
Articolo in rivista |
Vai |
| 2015 |
Efficacy and safety of alirocumab in reducing lipids and cardiovascular events |
Articolo in rivista |
Vai |
| 2015 |
Treating homozygous familial hypercholesterolemia in a real-world setting: Experiences with lomitapide |
Articolo in rivista |
Vai |
| 2015 |
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia |
Articolo in rivista |
Vai |
| 2015 |
The effect of ezetimibe on NAFLD |
Articolo in rivista |
Vai |
| 2015 |
Familial hypercholesterolæmia in children and adolescents: Gaining decades of life by optimizing detection and treatment |
Articolo in rivista |
Vai |
| 2015 |
Exome sequencing in suspected monogenic dyslipidemias |
Articolo in rivista |
Vai |
| 2015 |
Role of Nutraceuticals in Hypolipidemic Therapy |
Articolo in rivista |
Vai |
| 2015 |
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach |
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 |
The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia - A post-hoc analysis of a Phase 3, single-arm, open-label trial |
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 |
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE |
Proceedings |
Vai |
| 2014 |
eNOS activation by HDL is impaired in genetic CETP deficiency |
Articolo in rivista |
Vai |
| 2014 |
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS |
Proceedings |
Vai |
| 2014 |
Lomitapide: a novel drug for homozygous familial hypercholesterolemia |
Articolo in rivista |
Vai |
| 2014 |
Oxidative status in metabolic syndrome |
Proceedings |
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 |
The use of statins in people at risk of developing diabetes mellitus: Evidence and guidance for clinical practice |
Articolo in rivista |
Vai |
| 2014 |
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH |
Proceedings |
Vai |
| 2014 |
Gelatinases and their tissue inhibitors in metabolic syndrome |
Proceedings |
Vai |
| 2014 |
Behavior of the total antioxidant status in a group of subjects with metabolic syndrome. |
Articolo in rivista |
Vai |
| 2014 |
Clinical experience of lomitapide therapy in patients with homozygous familial hypercholesterolaemia |
Articolo in rivista |
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 |
| 2014 |
Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society |
Articolo in rivista |
Vai |
| 2014 |
Nuove linee guida americane 2013 ACC/AHA
sul trattamento del colesterolo plasmatico per ridurre il rischio cardiovascolare aterosclerotico: confronto con le raccomandazioni ESC/EAS per la gestione delle dislipidemie |
Articolo in rivista |
Vai |
| 2014 |
Study of the Correlations among Some Parameters of the Oxidative Status, Gelatinases, and Their Inhibitors in a Group of Subjects with Metabolic Syndrome |
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 |
| 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 |
FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA |
Proceedings |
Vai |
| 2013 |
A NOVEL APOB MUTATION IDENTIFIED
BY EXOME SEQUENCING COSEGREGATES
WITH STEATOSIS, LIVER CANCER
AND HYPOCHOLESTEROLEMIA |
Proceedings |
Vai |
| 2013 |
LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C |
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 |
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 |
Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society |
Articolo in rivista |
Vai |
| 2013 |
Protein oxidation in a group of subjects with metabolic syndrome. |
Articolo in rivista |
Vai |
| 2013 |
Oxidative status in nondiabetic middle-aged subjects with metabolic syndrome: preliminary data. |
Articolo in rivista |
Vai |
| 2013 |
Familial combined hypolipidemia due to mutations in the ANGPTL3 gene |
Articolo in rivista |
Vai |
| 2013 |
Efficacy and Safety of Ezetimibe Added to Atorvastatin Versus Atorvastatin Uptitration or Switching to Rosuvastatin in Patients With Primary Hypercholesterolemia |
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 |
The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management. |
Articolo in rivista |
Vai |
| 2013 |
LINEE GUIDA CLINICHE PER LA PREVENZIONE DELLA CARDIOPATIA ISCHEMICA NELLA IPERCOLESTEROLEMIA FAMILIARE
Una patologia sotto-diagnosticata e sotto-trattata |
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 |
OLESTEROLO: UNA MOLECOLA "MOLTO CONTROLLATA" |
Recensione in rivista |
Vai |
| 2013 |
REDUCTION OF CHOLESTEROL WITH NUTRACEUTICAL: RESULTS OF A DOUBLE BLIND STUDY |
Proceedings |
Vai |
| 2012 |
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL |
Proceedings |
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 |
Clinical utility of novel biomarkers for cardiovascular disease risk stratification |
Articolo in rivista |
Vai |
| 2012 |
Lipid-Altering Efficacy of Ezetimibe/Simvastatin 10/20 mg Compared to Rosuvastatin 10 mg in High-Risk Patients with and without Type 2 Diabetes Mellitus Inadequately Controlled Despite Prior Statin Monotherapy. |
Articolo in rivista |
Vai |
| 2012 |
Prothrombotic gene variants in AMI young women |
Proceedings |
Vai |
| 2012 |
Statin therapy in patients with aortic stenosis after the ASTRONOMER trial: is there still any space? |
Articolo in rivista |
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 |
Lipid and apoprotein composition of HDL in partial or complete CETP deficiency |
Articolo in rivista |
Vai |
| 2012 |
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. |
Articolo in rivista |
Vai |
| 2012 |
IL PROGETTO LIPIGEN: UN AGGIORNAMENTO |
Articolo in rivista |
Vai |
| 2012 |
Evaluation of nitric oxide metabolites in a group of subjects with metabolic syndrome. |
Articolo in rivista |
Vai |
| 2012 |
The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population |
Proceedings |
Vai |
| 2011 |
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY
ACIDS |
Proceedings |
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 |
Metabolomic analysis of plasma from Alzheimer disease patients |
Proceedings |
Vai |
| 2011 |
PREVALENCE OF ANGPTL3 AND APOB
GENE MUTATIONS IN SUBJECTS WITH
COMBINED HYPOLIPIDEMIA |
Proceedings |
Vai |
| 2011 |
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia |
Articolo in rivista |
Vai |
| 2011 |
PREVALENCE OF 'BORDERLINE' VALUES OF CARDIOVASCULAR RISK FACTORS IN THE CLINICAL PRACTICE OF GENERAL MEDICINE IN ITALY: RESULTS OF THE BORDERLINE STUDY. |
Articolo in rivista |
Vai |
| 2011 |
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY |
Articolo in rivista |
Vai |
| 2011 |
A genetic variant of the atrial natriuretic peptide gene is associated with cardiometabolic protection in the general community |
Articolo in rivista |
Vai |
| 2011 |
Hypobetalipoproteinemia: genetics, biochemistry, and clinical spectrum. |
Articolo in rivista |
Vai |
| 2011 |
SWITCHING FROM STATIN MONOTHERAPY TO EZETIMIBE/SIMVASTATIN OR ROSUVASTATIN MODIFIES THE RELATIONSHIPS BETWEEN APOLIPOPROTEIN B, LDL CHOLESTEROL, ANC NON-HDL CHOLETEROL IN PATIENTS AT HIGH RISK OF CORONARY DISEASE |
Articolo in rivista |
Vai |
| 2011 |
Identification of a novel mutation of MTP gene in a patient with abetalipoproteinemia. |
Articolo in rivista |
Vai |
| 2011 |
Le Dislipidemie Genetiche. Il Progetto LIPIGEN |
Articolo in rivista |
Vai |
| 2011 |
Lipid-altering efficacy of switching to ezetimibe/simvastatin 10/20 mg versus rosuvastatin 10 mg in high-risk patients with and without metabolic syndrome |
Articolo in rivista |
Vai |
| 2010 |
Modification of the lipidic and coagulative pattern in postmenopause women: effect of hormone replacement therapy. |
Articolo in rivista |
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 |
Ezetimibe/simvastatin 10/20 mg versus simvastatin 40 mg in coronary heart disease patients |
Articolo in rivista |
Vai |
| 2010 |
Compliance al trattamento in un paziente in terapia ipocolesterlemizzante |
Articolo in rivista |
Vai |
| 2010 |
Postprandial hyperglycemia is a determinant of platelet activation in early type 2 diabetes mellitus. |
Articolo in rivista |
Vai |
| 2010 |
Il paziente con SCA dopo dimissione dall'ospedale: terapia di mantenimento con statine |
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 |
Effects of PCSK9 variants on common carotid artery intima media thickness and relation to ApoE alleles. |
Articolo in rivista |
Vai |
| 2010 |
Paziente con obesità viscelare, asintomatico |
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 |
Ezetimibe/Simvastatin 10/20 mg versus Rosuvastatin 10 mg in high-risk hypercholesterolemic patients stratified by prior statin treatment potency. |
Articolo in rivista |
Vai |
| 2010 |
POSTPRANDIAL HYPERGLYCEMIA IS A DETERMINANT OF PLATELET ACTIVATION IN EARLY 2 DIABETES MELLITUS |
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 |
Il paziente anziano |
Articolo in rivista |
Vai |
| 2009 |
Dislipidemia della sindrome metabolica . fisiopatologia e clinica |
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 |
Lipid-altering efficacy of ezetimibe/simvastatin 10/20 mg compared with rosuvastatin 10 mg in high-risk hypercholesterolaemic patients inadequately controlled with prior statin monotherapy - The IN-CROSS study. |
Articolo in rivista |
Vai |
| 2009 |
Obesity and the metabolic syndrome in a student cohort from Southern Italy |
Articolo in rivista |
Vai |
| 2009 |
La supplementazione con substrati pro-energetivi nel soggetto astenico |
Articolo in rivista |
Vai |
| 2009 |
Effects of a phytosterol-enriched dairy product on lipids, sterols and 8-isoprostane in hypercholesterolemic patients: A multicenter Italian study. |
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 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 |
Marker dell'infiammazione : quali le implicazioni degli studi più recenti? |
Articolo in rivista |
Vai |
| 2009 |
Paziente con infarto miocardico, bassa colesterolemia e aumentali livelli PCR |
Articolo in rivista |
Vai |
| 2008 |
Lo studio Corona: un commento |
Articolo in rivista |
Vai |
| 2008 |
Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient |
Articolo in rivista |
Vai |
| 2008 |
Dietary cholesterol and estrogen administration elevate brain apolipoprotein E in mice by different mechanisms |
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 |
Paziente donna a elevatissimo rischio cardiovascolare |
Abstract in rivista |
Vai |
| 2008 |
PATIENT PROFILE: UN PAZIENTE CON FENOTIPO LIPOPROTEICO ATEROGENO |
Articolo in rivista |
Vai |
| 2007 |
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. |
Proceedings |
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 |
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 |
NUOVE DISPOSIZIONI DELLA NOTA 13 PER PAZIENTI HIV-POSITIVI IN TERAPIA ANTIRETROVIALE E PER PAZIENTI CON INSUFFICIENZA RENALE CRONICA |
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 |
Proceedings |
Vai |
| 2007 |
INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). |
Proceedings |
Vai |
| 2007 |
MUTATIONS IN THE CETP GENE IN ITALIAN SUBJECTS WITH HYPERALPHALIPOPROTEINEMIA |
Proceedings |
Vai |
| 2007 |
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL |
Proceedings |
Vai |
| 2007 |
Genetics of familial hypobetalipoproteinemia |
Articolo in rivista |
Vai |
| 2007 |
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? |
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 |
LE IPERCOLESTEROLEMIE PRIMITIVE |
Articolo in rivista |
Vai |
| 2007 |
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE |
Proceedings |
Vai |
| 2007 |
PATIENT PROFILE: PAZIENTE AD ALTISSIMO RISCHIO CARDIOVASCOLARE CON ADERENZA INSUFFICIENTE ALLA TERAPIA |
Articolo in rivista |
Vai |
| 2007 |
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA |
Articolo in rivista |
Vai |
| 2007 |
GENETIC HETEROGENEITY OF SEVERE HYPOBETALIPOPROTEINEMIA |
Proceedings |
Vai |
| 2007 |
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA |
Articolo in rivista |
Vai |
| 2007 |
EZETIMIBE: QUALE RUOLO ALLA LUCE DELLE NUOVE LINEE GUIDA? |
Articolo in rivista |
Vai |
| 2007 |
FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. |
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 |
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 |
Proceedings |
Vai |
| 2007 |
The PCSK9 gene: a new gene controlling cholesterolemia |
Articolo in rivista |
Vai |
| 2007 |
Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins |
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 |
Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study |
Articolo in rivista |
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 |
A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 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 |
Use of stents with sirolimus is significantly associated with a reduction in mortality and cardiovascular morbidity at 6- and 12-months post-PTCA |
Abstract in rivista |
Vai |
| 2006 |
PATIENT PROFILE: PAZIENTE NEFROPATICO, PAZIENTE GIOVANE CON DIABETE, PAZIENTE DONNA, PAZIENTE IN ETÀ pediatrica |
Articolo in rivista |
Vai |
| 2006 |
PREVALENCE OF A METABOLIC SYNDROME AMONG A PEDIATRIC CASISTIC FROM THE MOUNTAIN COMMUNITY (SERRE CALABRE). |
Proceedings |
Vai |
| 2006 |
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA |
Proceedings |
Vai |
| 2006 |
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent |
Articolo in rivista |
Vai |
| 2006 |
Additive effect of mutations in LDLR and PCSK9 genes on the phenotyoe of familial hypercholesterolemia |
Articolo in rivista |
Vai |
| 2006 |
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS |
Proceedings |
Vai |
| 2006 |
VARIABLE PHENOTYPIC ESPRESSION IN A LIPID ABSORPTION DISORDER DUE TO A MOLECULAR DEFECT IN THE SARA2 GENE |
Proceedings |
Vai |
| 2006 |
L’uso di stent con sirolimus e’ significativamente associate alla riduzione della mortalita’ totale e della morbidita’ cardiovascolare sia a 6 mesi che a 12 mesi post-PTCA. |
Abstract in rivista |
Vai |
| 2006 |
Association between apolipoprotein E epsilon4 allele and apathy in probable Alzheimer's disease. |
Articolo in rivista |
Vai |
| 2006 |
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE |
Proceedings |
Vai |
| 2006 |
The c.43_44insCTG variation in PCSK9 is associated with low plasma LDL-cholesterol in a Caucasian population. |
Articolo in rivista |
Vai |
| 2006 |
A Targeted ApoB38.9 Mutation in Mice Is Associated with Reduced Hepatic Cholesterol Synthesis and Enhanced Lipid Peroxidation. |
Articolo in rivista |
Vai |
| 2006 |
EZETIMIBE: WHAT ROLE in the light of recent guidelines |
Articolo in rivista |
Vai |
| 2006 |
Gene expression in mouse spermatogenesis during ontogenesis. |
Articolo in rivista |
Vai |
| 2006 |
CLINICAL AND RESEARCH CONCEPTS: LE BARRIERE LEGATE AL PAZIENTE |
Articolo in rivista |
Vai |
| 2006 |
Analysis of sterols by high-performance liquid chromatography/mass spectrometry combined with chemometrics |
Articolo in rivista |
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 |
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease |
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 |
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults |
Articolo in rivista |
Vai |
| 2006 |
A Novel Liquid Chromatography/Mass Spectrometry Method for Analysis of Plasma Sterol Concentrations |
Proceedings |
Vai |
| 2006 |
CLINICAL AND RESEARCH CONCEPTS: GENETICA DELLE DISLIPIDEMIE (LE IPERCOLESTEROLEMIE) |
Articolo in rivista |
Vai |
| 2006 |
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues |
Articolo in rivista |
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 |
THERAPEUTIC LIFESTYLE CHANGES: L’ALIMENTAZIONE |
Articolo in rivista |
Vai |
| 2005 |
Bovine seminal ribonuclease is cytotoxic for both malignant and normal telomerase-positive cells |
Articolo in rivista |
Vai |
| 2005 |
ADDITIVE EFFECT OF MUTATIONS IN LDLR AND PCSK9 GENES ON THE PHENOTYPE OF FAMILIAL HYPERCHOLESTEROLEMIA. |
Proceedings |
Vai |
| 2005 |
Drug eluting stents's use in patients with anatomical or clinical patterns favouring restenosis: a 6-months follow-up study |
Proceedings |
Vai |
| 2005 |
MUSCLE DAMAGE AND PAIN IN HYPERCHOLESTEROLEMIC OUT-PATIENTS POPULATION ON STATIN TREATMENT. |
Proceedings |
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 |
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 |
FAMILIAL HYPOALPHALIPOPROTEINEMIA ASSOCIATED TO CORNEAL OPACITIES IN ABSENCE OF LCAT DEFICIENCY |
Proceedings |
Vai |
| 2005 |
GASTROINTESTINAL SYMPTOMS IN INFANCY: A POPULATION-BASED PROSPECTIVE STUDY |
Articolo in rivista |
Vai |
| 2005 |
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA |
Proceedings |
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 |
Cystatin C levels are decreased in acute myocardial infarction: Effect of cystatin C G73A gene polymorphism on plasma levels |
Articolo in rivista |
Vai |
| 2005 |
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT |
Proceedings |
Vai |
| 2005 |
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia. |
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 |
Relazione tra il size delle LDL e l’estensione della malattia vasale coronarica in 72 pazienti maschi sottoposti a coronarografia diagnostica |
Abstract 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 |
Chronic constipation and food intolerance: a model of proctitis causing constipation |
Articolo in rivista |
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 |
Anti-actin antibodies in celiac disease: correlation with intestinal mucosa damage and comparison of ELISA with the immunofluorescence assay. |
Articolo in rivista |
Vai |
| 2005 |
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING IN THE LDL-R GENE AND IN THE PCSK9 GENE |
Proceedings |
Vai |
| 2005 |
CLINICAL AND RESEARCH CONCEPTS: NUTRIZIONE E METABOLISMO |
Articolo in rivista |
Vai |
| 2005 |
Drug eluting stents's use in patients with anatomical or clinical patterns favouring restenosis: a 6-months follow-up study. Atherosclerosis. 2005. 6(suppl.1) |
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 |
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia |
Articolo in rivista |
Vai |
| 2004 |
A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke |
Articolo in rivista |
Vai |
| 2004 |
MUTAZIONI DEL GENE DELL’APOB RESPONSABILI DI IPOBETALIPOPROTEINEMIA FAMILIARE IN SICILIA |
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 |
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 |
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 |
FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE |
Proceedings |
Vai |
| 2004 |
Use of the drug eluting stents with rapamicin in patients with anatomical or clinical patterns favouring restenosis: results of a 6-months follow-up on the first 100 patients |
Abstract in rivista |
Vai |
| 2004 |
MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. |
Proceedings |
Vai |
| 2004 |
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA |
Proceedings |
Vai |
| 2004 |
NONSENSE MUTATION IN THE CETP 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 |
| 2004 |
PREVALENCE OF METABOLIC SYNDROME IN A RURAL SICILIAN POPULATION AND RELATIONS WITH CLINICAL EVENTS: THE VENTIMIGLIA HEART PROJECT. |
Proceedings |
Vai |
| 2004 |
FAMILIAL HDL DEFICIENCY DUE TO ABCA1 GENE MUTATIONS WITH OR WITHOUT OTHER GENETIC LIPOPROTEIN DISORDERS |
Articolo in rivista |
Vai |
| 2004 |
Genetic risk factors in myocardial infarction at young age. Minerva Cardioangiol. 2004 Aug;52(4):287-312 |
Articolo in rivista |
Vai |
| 2004 |
Genetic risk factors in myocardial infarction at young age. |
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 |
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects |
Proceedings |
Vai |
| 2004 |
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY |
Proceedings |
Vai |
| 2004 |
BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES |
Articolo in rivista |
Vai |
| 2004 |
MALABSORPTION OF FAT IN CELIAC DISEASE DURING AN ORAL FAT LOAD. KINETIC STUDY OF CHYLOMICRONS AND REMNANTS AND CORRELATION WITH THE STAGE OF THE DISEASE |
Proceedings |
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 |
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. |
Proceedings |
Vai |
| 2004 |
USE OF THE DRUG ELUTING STENTS WITH RAPAMICIN IN PATIENTS WITH ANATOMICAL OR CLINICAL PATTERNS FAVOURING RESTENOSIS: RESULTS OF A 6-MONTHS FOLLOW-UP ON THE FIRST 100 PATIENS. |
Proceedings |
Vai |
| 2004 |
Risultati del follow-up di 6 mesi in 100 pazienti con stent medicato con rapamicina rispetto ad altri 100 con stent tradizionale |
Abstract in rivista |
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 |
AN HPLC/APCI METHOD, USING PARTLY MISCIBLE SOLVENTS, FOR A SIMPLE SEPARATION AND DETERMINATION OF STEROLS IN BLOOD |
Proceedings |
Vai |
| 2003 |
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. |
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 |
Diagnostic accuracy of fecal calprotectin assay in distinguishing organic causes of chronic diarrhea from irritable bowel syndrome: a prospective study in adults and children |
Articolo in rivista |
Vai |
| 2003 |
Association between HFE mutations and acute myocardial infarction: a study in patients from Northern and Southern Italy |
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 |
Screening for celiac disease in non-Hodgkin's lymphoma patients: a serum anti-transglutaminase-based approach |
Articolo in rivista |
Vai |
| 2003 |
Autoimmune enteropathy and colitis in an adult patient |
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 |
Fatty liver in familial hypobetalipoproteinemia: Triglyceride assembly into VLDL particles is affected by the extent of hepatic steatosis |
Articolo in rivista |
Vai |
| 2002 |
Lack of association between angiotensin converting enzyme polymorphism and sporadic Alzheimer's disease |
Articolo in rivista |
Vai |
| 2002 |
Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds |
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 |
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 |
| 2002 |
Comparison of anti-transglutaminase ELISAs and an anti-endomysial antibody assay in the diagnosis of celiac disease: A prospective study |
Articolo 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 |
Determinants of enhanced thromboxane biosynthesis in renal transplantation |
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 |
Estrogen increases hepatic lipase levels in inbred strains of mice: A possible mechanism for estrogen-dependent lowering of high density lipoprotein |
Articolo in rivista |
Vai |
| 2001 |
Carotid atherosclerosis in hypercholesterolemic patients: Relationship with cardiovascular events |
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 |
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 |
Dietary cholate increases plasma levels of apolipoprotein B in mice by posttranscriptional mechanisms |
Articolo in rivista |
Vai |
| 1999 |
Lipoprotein(a) levels in relation to albumin concentration in childhood nephrotic syndrome |
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 |
| 1996 |
A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: Genetic and metabolic studies |
Articolo in rivista |
Vai |
| 1995 |
Plasma levels of lipoproteins and apolipoproteins in congenital hypothyroidism: effects of L-thyroxine substitution therapy |
Articolo in rivista |
Vai |
