| 2022 |
Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients |
Articolo in rivista |
Vai |
| 2022 |
Progressive right ventricular dysfunction and exercise impairment in patients with heart failure and diabetes mellitus: insights from the T.O.S.CA. Registry |
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 |
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 |
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 |
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 |
| 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 |
PREVALENCE OF STATIN INTOLERANCE IN A COHORT OF OUTPATIENTS IN A LIPID CLINIC |
Abstract in atti di convegno pubblicato in rivista |
Vai |
| 2018 |
The complex alteration in the network of IL-17-type cytokines in patients with hereditary angioedema |
Articolo in rivista |
Vai |
| 2018 |
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred |
Articolo in rivista |
Vai |
| 2018 |
Multiple hormonal and metabolic deficiency syndrome in chronic heart failure: rationale, design, and demographic characteristics of the T.O.S.CA. Registry |
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 |
| 2016 |
Detectable interleukin-9 plasma levels are associated with impaired cardiopulmonary functional capacity and all-cause mortality in patients with chronic heart failure |
Articolo in rivista |
Vai |
| 2016 |
Genetic epidemiology of ARH in Sicily |
Abstract in atti di convegno pubblicato in rivista |
Vai |
| 2016 |
Growth factors and IL-17 in hereditary angioedema |
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 |
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS |
Proceedings |
Vai |
| 2014 |
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE |
Proceedings |
Vai |
| 2014 |
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH |
Proceedings |
Vai |
| 2014 |
Visceral Adiposity Index (VAI) Is Predictive of an Altered Adipokine Profile in Patients with Type 2 Diabetes |
Articolo in rivista |
Vai |
| 2014 |
Upregulation of cytokines and IL-17 in patients with hereditary angioedema |
Articolo in rivista |
Vai |
| 2013 |
Visceral Adiposity Index (VAI) as a simple indicator of “adipose tissue dysfunction” in patients with type 2 diabetes. |
Proceedings |
Vai |
| 2012 |
Cytokine serum profile in a group of Sicilian Nonagenarians |
Articolo in rivista |
Vai |
| 2012 |
Analysis of the Polymorphisms of Th1 and Th17 Cytokines in Mediterranean Spotted Fever |
Proceedings |
Vai |
| 2012 |
Analysis of IL-6, IL-10 and IL-17 genetic polymorphisms as risk factors for sepsis development in burned patients. |
Articolo in rivista |
Vai |
| 2012 |
Training Effects on Laboratory Parameters Are Independent of Genetic Polymorphisms of IL-10 and TNF-alpha (TNF-α) |
Proceedings |
Vai |
| 2012 |
Single nucleotide polymorphisms (SNPs) of pro-inflammatory/anti-inflammatory and thrombotic/fibrinolytic genes in patients with acute ischemic stroke in relation to TOAST subtype |
Articolo in rivista |
Vai |
| 2011 |
Role of prothrombotic polymorphisms in successful or unsuccessful aging |
Articolo in rivista |
Vai |
| 2011 |
The T.O.S.C.A. Project: Research, Education and Care |
Articolo in rivista |
Vai |
| 2010 |
Systemic Immune Responses in Alzheimer’s
Disease: In Vitro Mononuclear Cell
Activation and Cytokine Production |
Articolo in rivista |
Vai |
| 2009 |
Relevance of gamma interferon, tumor necrosis factor alpha, and interleukin-10 gene polymorphisms to susceptibility to Mediterranean spotted fever. |
Articolo in rivista |
Vai |
| 2008 |
Aminobisphosphonate-activated gammadelta T cells in immunotherapy of cancer:
doubts no more. |
Articolo in rivista |
Vai |
| 2004 |
C4BQ0: a genetic marker of familial HCV-related liver cirrhosis. |
Articolo in rivista |
Vai |
| 2004 |
Up-regulation of c-FLIPshort and Reduction of Activation-Induced Cell Death in T-cells from Patients with Type 1 Diabetes |
Articolo in rivista |
Vai |
