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GABRIELLA MISIANO

Pubblicazioni

Data Titolo Tipologia Scheda
2022 Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients 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 MUTATION IN CANDIDATE GENES ACCOUNT FOR A SMALL MINORITY OF HYPOBETALIPOPROTEINEMIAS AND NGS ANALYSIS SUPPORT POLYGENICITY IN MUTATION-NEGATIVE PATIENTS Abstract in atti di convegno pubblicato in rivista Vai
2020 MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" Abstract in atti di convegno pubblicato in rivista Vai
2020 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 Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred Articolo 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 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 Proceedings (TIPOLOGIA NON ATTIVA) Vai
2016 Genetic epidemiology of ARH in Sicily Proceedings (TIPOLOGIA NON ATTIVA) 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 Growth factors and IL-17 in hereditary angioedema Articolo in rivista Vai
2014 Upregulation of cytokines and IL-17 in patients with hereditary angioedema Articolo in rivista Vai
2014 DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH Proceedings (TIPOLOGIA NON ATTIVA) Vai
2014 Visceral Adiposity Index (VAI) Is Predictive of an Altered Adipokine Profile in Patients with Type 2 Diabetes 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 (TIPOLOGIA NON ATTIVA) Vai
2014 RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE Proceedings (TIPOLOGIA NON ATTIVA) Vai
2014 NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS Proceedings (TIPOLOGIA NON ATTIVA) Vai
2013 Visceral Adiposity Index (VAI) as a simple indicator of “adipose tissue dysfunction” in patients with type 2 diabetes. Proceedings (TIPOLOGIA NON ATTIVA) Vai
2012 Analysis of the Polymorphisms of Th1 and Th17 Cytokines in Mediterranean Spotted Fever Proceedings (TIPOLOGIA NON ATTIVA) 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
2012 Cytokine serum profile in a group of Sicilian Nonagenarians Articolo in rivista 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 (TIPOLOGIA NON ATTIVA) Vai
2011 The T.O.S.C.A. Project: Research, Education and Care Articolo in rivista Vai
2011 Role of prothrombotic polymorphisms in successful or unsuccessful aging 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 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
2004 C4BQ0: a genetic marker of familial HCV-related liver cirrhosis. Articolo in rivista Vai