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CONCETTA SCAZZONE

Pubblicazioni

Data Titolo Tipologia Scheda
2024 Evaluation of core Biomarkers of Alzheimer’s disease in saliva and plasma measured by chemiluminescent enzyme immunoassays on a fully automated platform Articolo in rivista Vai
2024 Clinical usefulness of presepsin and monocyte distribution width (MDW) kinetic for predicting mortality in critically ill patients in intensive care unit Articolo in rivista Vai
2024 The role of Killer immunoglobulin-like receptors (KIRs) in the genetic susceptibility to non-celiac wheat sensitivity (NCWS) Articolo in rivista Vai
2024 A machine learning strategy to mitigate the inappropriateness of procalcitonin request in clinical practice Articolo in rivista Vai
2024 Exploring the effect of APOE ε4 on biomarkers of neurodegeneration in Alzheimer’s disease Articolo in rivista Vai
2023 Evaluation of the analytical performance of three chemiluminescence serological assays for detecting anti-SARS-CoV-2 antibodies Articolo in rivista Vai
2023 Detection of Antibodies against the Acetylcholine Receptor in Patients with Myasthenia Gravis: A Comparison of Two Enzyme Immunoassays and a Fixed Cell-Based Assay Articolo in rivista Vai
2023 Monocyte distribution width (MDW) in sepsis Review essay (rassegna critica) Vai
2023 Monocyte Distribution Width (MDW) as a biomarker of sepsis: An evidenced-based laboratory medicine approach Review essay (rassegna critica) Vai
2023 Microglial Activation and Priming in Alzheimer’s Disease: State of the Art and Future Perspectives Review essay (rassegna critica) Vai
2023 Microglial Activation and Priming in Alzheimer’s Disease: State of the Art and Future Perspectives Review essay (rassegna critica) Vai
2023 Multiple Sclerosis Pathogenesis: Possible Interplay between Vitamin D Status and Epstein Barr Virus Infection Nota o commento Vai
2022 Role of Multiple Vitamin D-Related Polymorphisms in Multiple Sclerosis Severity: Preliminary Findings Articolo in rivista Vai
2022 Serum Vitamin D as a Biomarker in Autoimmune, Psychiatric and Neurodegenerative Diseases Review essay (rassegna critica) Vai
2022 Monocyte distribution width (MDW) as a screening tool for early detecting sepsis: a systematic review and meta-analysis Articolo in rivista Vai
2022 Evaluation of Alpha-Synuclein Cerebrospinal Fluid Levels in Several Neurological Disorders Articolo in rivista Vai
2021 Validation of monocyte distribution width decisional cutoff for sepsis detection in the acute setting Lettera Vai
2021 Vitamin D and Genetic Susceptibility to Multiple Sclerosis Review essay (rassegna critica) Vai
2021 COVID-19 and Alzheimer's Disease Review essay (rassegna critica) Vai
2021 Comparative analysis of biochip mosaic-based indirect immunofluorescence with enzyme-linked immunosorbent assay for diagnosing myasthenia gravis Articolo in rivista Vai
2021 A new tool for sepsis screening in the Emergency Department Articolo in rivista Vai
2021 Neurogranin as a Reliable Biomarker for Synaptic Dysfunction in Alzheimer’s Disease Articolo in rivista Vai
2021 The Value of a Complete Blood Count (CBC) for Sepsis Diagnosis and Prognosis Review essay (rassegna critica) Vai
2021 Evaluation of anti-sars-cov-2 s-rbd igg antibodies after covid-19 mrna bnt162b2 vaccine Articolo in rivista Vai
2021 Clinical Utility of Midregional Proadrenomedullin in Patients with COVID-19 Articolo in rivista Vai
2021 Preliminary reference intervals of Glycated Albumin in healthy Caucasian pregnant women Articolo in rivista Vai
2021 The role of vitamin d as a biomarker in alzheimer’s disease Review essay (rassegna critica) Vai
2021 Foxp3 and gata3 polymorphisms, vitamin d3 and multiple sclerosis Articolo in rivista Vai
2020 Klotho and vitamin D in multiple sclerosis: an Italian study Articolo in rivista Vai
2020 Clinical Use of κ Free Light Chains Index as a Screening Test for Multiple Sclerosis Articolo in rivista Vai
2020 Monocyte distribution width (MDW) as a screening tool for sepsis in the Emergency Department Articolo in rivista Vai
2019 Establishing the 99th percentile for high sensitivity cardiac troponin i in healthy blood donors from southern italy Articolo in rivista Vai
2019 Fructose-1,6-Bisphosphate Protects Hippocampal Rat Slices from NMDA Excitotoxicity Articolo in rivista Vai
2019 Vitamin D increases the production of IL-10 by regulatory T cells in patients with systemic sclerosis Articolo in rivista Vai
2019 Vitamin D in malaria: more hypotheses than clues Articolo in rivista Vai
2019 Vitamin D and Multiple Sclerosis: An Open-Ended Story Articolo in rivista Vai
2019 Proton-irradiated breast cells: molecular points of view Articolo in rivista Vai
2019 Non-skeletal activities of vitamin d: From physiology to brain pathology Articolo in rivista Vai
2019 Standardized measurement of circulating vitamin D [25(OH)D] and its putative role as a serum biomarker in Alzheimer's disease and Parkinson's disease Articolo in rivista Vai
2019 Body mass index and impact on semen quality of men attending an infertility clinic Articolo in rivista Vai
2019 Reference interval by the indirect approach of serum thyrotropin (TSH) in a Mediterranean adult population and the association with age and gender Articolo in rivista Vai
2018 CYP27A1, CYP24A1, and RXR-α Polymorphisms, Vitamin D, and Multiple Sclerosis: a Pilot Study Articolo in rivista Vai
2018 A new role of CYP2R1 in Multiple Sclerosis Articolo in rivista Vai
2018 Association of CYP2R1 rs10766197 with MS risk and disease progression Articolo in rivista Vai
2017 Galectin-3 in acute coronary syndrome Review essay (rassegna critica) Vai
2017 VDBP, CYP27B1, and 25-Hydroxyvitamin D Gene Polymorphism Analyses in a Group of Sicilian Multiple Sclerosis Patients Articolo in rivista Vai
2017 The cervical fracture as first symptom of multiple myeloma: A case report Articolo in rivista Vai
2017 Establishing the upper reference limit of Galectin-3 in healthy blood donors Articolo in rivista Vai
2017 Heart-type fatty acid binding protein is a sensitive biomarker for early AMI detection in troponin negative patients: a pilot study Articolo in rivista Vai
2016 Utility of serum procalcitonin and C-reactive protein in severity assessment of community-acquired pneumonia in children Articolo in rivista Vai
2016 Fetuin-A is Associated to Serum Calcium and AHSG T256S Genotype but Not to Coronary Artery Calcification Articolo in rivista Vai
2016 Association between hypovitaminosis D and systemic sclerosis: True or fake? Review essay (rassegna critica) Vai
2016 Erratum: Corrigendum to “Procalcitonin and community-acquired pneumonia (CAP) in children” (Clinica Chimica Acta (2015) 451(Part B) (215–218) (S0009898115004404) (10.1016/j.cca.2015.09.031)) Nota o commento Vai
2016 Short-term Changes in Gal 3 Circulating Levels After Acute Myocardial Infarction Articolo in rivista Vai
2016 Vitamin D receptor polymorphisms and 25-hydroxyvitamin D in a group of Sicilian multiple sclerosis patients Articolo in rivista Vai
2015 MTHFR C677T allelic variant is not associated to plasma and cerebrospinal fluid homocysteine in Amyotrophic Lateral Sclerosis Articolo in rivista Vai
2015 FOKI AND BSMI VITAMIN D RECEPTOR GENE POLYMORPHISMS, PLASMA RENIN ACTIVITY AND ESSENTIAL ARTERIAL HYPERTENSION Proceedings Vai
2015 Vitamin D receptor gene polymorphisms and plasma renin activity in essential hypertensive individuals Articolo in rivista Vai
2015 Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients. Articolo in rivista Vai
2015 FOKI AND BSMI VITAMIN D RECEPTOR GENE POLYMORPHISMS, ARE THEY ASSOCIATED WITH INTIMA MEDIA THICKNESS IN ESSENTIAL HYPERTENSIVE INDIVIDUALS Proceedings Vai
2015 Procalcitonin and community-acquired pneumonia (CAP) in children Articolo in rivista Vai
2014 Correlation between Low Folate Levels and Hyperhomocysteinemia, but not with Vitamin B12 in Hypertensive Patients. Articolo in rivista Vai
2014 Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia Articolo in rivista Vai
2014 I polimorfismi del gene VDR FokI e BsmI non sembrano essere associati all’ipertensione arteriosa Proceedings Vai
2014 VITAMIN D RECEPTOR FOKI AND BSMI POLYMORPHISMS DO NOT SEEM TO BE ASSOCIATED WITH ARTERIAL HYPERTENSION Proceedings Vai
2014 MTHFR C677T allelic variant is not associated to plasma and cerebrospinal fluid homocysteine in amyotrophic lateral sclerosis Proceedings Vai
2014 Vitamin K Deficit leads to Chronic Inflammatory Bowel Disease Diagnosis: a case report Proceedings Vai
2014 Effects of EPHX1 and CYP3A4 polymorphisms on carbamazepine metabolism in epileptic patients Articolo in rivista Vai
2013 CORRELAZIONE TRA ALDOSTERONE E PARATORMONE PLASMATICI NELL’IPERTENSIONE ARTERIOSA ESSENZIALE Proceedings Vai
2013 A case of Hepatitis C virus and mixed cryoglobulinemia in a patient with Kidney Disease Proceedings Vai
2013 Association of vitamin D serum levels and its common genetic determinants, with severity of liver fibrosis in genotype 1 chronic hepatitis C patients Articolo in rivista Vai
2013 The role of prothrombotic variants in acute ischemic stroke Proceedings Vai
2013 Effect of genetics polymorphism of carbamazepine – metabolizing enzymes in epileptic patients Proceedings Vai
2013 Detection of oncogenic human papillomavirus genotypes on spermatozoa from male partners of infertile couples Articolo in rivista Vai
2013 Association of vitamin D serum levels and its common genetic determinants with severity of liver fibrosis in genotype 1 chronic hepatitis C patients Proceedings Vai
2012 Vitamin D, blood pressure and intima media thickness in essential hypertension Proceedings Vai
2012 Vitamin D levels and IL28B polymorphisms are related to rapid virological response to standard of care in genotype 1 chronic hepatitis C. Articolo in rivista Vai
2011 LOW VITAMIN D SERUM LEVEL IS RELATED TO RAPID, EARLY AND SUSTAINED VIROLOGICAL RESPONSE TO IFN-BASED THERAPY IN GENOTYPE 1 CHRONIC HEPATITIS C Abstract in rivista Vai
2011 RELATIONSHIP BETWEEN VITAMIN D STATUS AND EARLY ARTERIAL CHANGES IN PRIMARY HYPERTENSION. PRELIMINARY DATA Proceedings Vai
2011 Study on the efficacy of Rapamicin as an inducer of fetal hemoglobin in primary erythroid cultures from patientes with hemoglobinopathies Capitolo o Saggio Vai
2011 Endothelial dysfunction and vitamin d status in essential hypertension, prelimary results Proceedings Vai
2011 Vitamina D, ipertensione arteriosa e sistema renina-angiotensina Proceedings Vai
2011 Vitamina D e biomarcatori di attivazione endoteliale e di infiammazione nell'ipertensione arteriosa essenziale Proceedings Vai
2010 LOW VITAMIN D SERUM LEVEL IS RELATED TO RAPID, EARLY AND SUSTAINED VIROLOGICAL RESPONSE TO IFN-BASED THERAPY IN GENOTYPE 1 CHRONIC HEPATITIS C Abstract in rivista Vai
2010 Low vitamin D serum level is related to severe fibrosis and low responsiveness to interferon-based therapy in genotype 1 chronic hepatitis C Articolo in rivista Vai
2009 Methionine synthase reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular disease. Articolo in rivista Vai
2009 Characterization of two alternative Interleukin(IL)-10 5_UTR mRNA sequences, induced by lipopolysaccharide (LPS) stimulation of peripheral blood mononuclear cells Articolo in rivista Vai
2009 Study on the efficacy of Rapamicin as an inducer of fetal hemoglobin in primary erythroid cultures from patientes with hemoglobinopathies Proceedings Vai
2008 Antioxidant activity in solution and biological membranes of seven cultivars of Sicilian peach (Prunus Persica, L. Mill). Proceedings Vai
2007 Effects of polymorphism of Methionine Synthase Reductase on total plasma homocysteine in Sicilian populations Proceedings Vai
2007 Factor V Leiden, Prothrombin G20210A mutations are risk factors for deep vein thrombosis Proceedings Vai
2007 Association between homocysteinemia and Metabolic Syndrome in patients with cardiovascular disease Articolo in rivista Vai
2007 Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase MTHFR A1298C gene polymorphism in subjects affected by thromboembolic disease Proceedings Vai
2007 Apo E polymorphism as risk factor for cardiovascular diseases in Sicilian subjects. Proceedings Vai
2007 Methionine synthase polymorphism A2756G and its association with thromboembolic disease Proceedings Vai
2007 The risk of cardiovascular events is reduced by lowering hyperhomocysteinemia short term B vitamins therapy Proceedings Vai
2007 GERD patients: a risk group for xerostomia and oral lesions? A case-control syudy Proceedings Vai
2007 Vitamin E and vitamin A plasma levels in patients with Mild Cognitive Impairent (MCI) Proceedings Vai
2007 Association between angiotensin I - converting enzyme gene insertion/deletion polymorphism and thromboembolic disease. Proceedings Vai
2007 Mutations in Factor V Leiden (G1691A) and Prothrombin (G2021A) genes are important risk factors for venous thromboembolism Proceedings Vai
2007 Potential role of Vitamin K2 plasma levels determination in Alzheimer's Disease Proceedings Vai
2007 Hyperhomocysteinemia and methylenetetrahydrofolare reductase 677C→T and 1298A→C mutations in patients with venous thromboembolic disease Proceedings Vai
2007 Changes in serum fetuin-A and inflammatory markers levels in end stage renal disease (ESRD): effect of a single session haemodialysis. Proceedings Vai
2006 Homocysteine and MTHFR gene polimorphysms in patients with venous tromboembolic disease Proceedings Vai
2006 Low Fetuin-A plasma levels are associated with the presence of carotid plaques in patients on dialysis. Proceedings Vai
2006 The Homocysteine System Articolo in rivista Vai
2006 Apoliprotein E gene polymorphism in subjects affected by cardiovascular disease in Sicilian populations Proceedings Vai
2006 Prevalence and association of the Factor V Leiden and Prothrombin G20210A in healthy subjects and patients with venous tromboembolism Proceedings Vai
2005 Metabolic sindrome and increased risk for cardiovascular disease Proceedings Vai
2005 Quantitative evaluation of oxidative stress status on peripheral blood in beta-thalassaemic patients by means of electron paramagnetic resonance spectroscopy Articolo in rivista Vai
2005 Methionine loading test and genetic risk factors in subjects affected by thromboembolic disease Proceedings Vai
2005 Effect of MTHFR polymorphism on homocysteine level after Methionine loading in thromboembolic patients. Proceedings Vai
2005 Nutrienti nella prevenzione dello Stress Ossidativo Articolo in rivista Vai
2005 Biochimica e Fisiopatologia delle Specie Reattive dell’Ossigeno Articolo in rivista Vai
2005 Evaluation of plasma homocysteine levels and metabolic sindrome in patients with cardiovascular disease Proceedings Vai
2004 Evaluations and new relationships between renal failure and homocysteine plasma levels in patients with chronic renal failure Proceedings Vai
2004 Plasma homocysteine levels in patients with chronic renal failure. Proceedings Vai
2004 Genetic analysis about the wellknown relationship between Alzheimer Demaentia outbreak and APP gene overexpression in Down young patients Proceedings Vai
2004 Evaluations and new relationship between renal failure and homocysteine plasma levels in patients with chronic renal failure. Proceedings Vai
2004 Curva da carico orale di metionina nella valutazione di pazienti affetti da patologia trombotica Proceedings Vai
2004 Valutazione dei livelli ematici di omocisteina, acido folico, vitamine B6 e B12 in soggetti anziani con funzioni cognitive alterate in seguito a stroke Proceedings Vai
2004 Genetic testing on Dry Blood Spot Card samples of Sicilian people in aim to check out the ΔR 608 mutation causing Niemann-Pick Disease Type B. Proceedings Vai
2004 Evaluation of patients with thrombotic stroke by methionine loading oral curve Proceedings Vai
2004 Plasma omocysteine levels in patients with chronic renal failure Proceedings Vai
2004 Plasma homocysteine levels in patients with chronic renal failure Proceedings Vai