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CHIARA BELLIA

Curriculum e ricerca

Contatti

chiara.bellia@unipa.it

Curriculum non disponibile

Insegnamenti

Anno accademico Codice della materia Nome della materia CFU Corso di studi
2023/2024 90404 BIOCHIMICA CLINICA (MODULO) 3 SCIENZE DELLE PROFESSIONI SANITARIE TECNICHE DIAGNOSTICHE
2023/2024 96606 BIOCHIMICA CLINICA (MODULO) 4 TECNICHE DI LABORATORIO BIOMEDICO (ABILITANTE ALLA PROFESSIONE SANITARIA DI TECNICO DI LABORATORIO BIOMEDICO)
2023/2024 21908 BIOCHIMICA CLINICA C.I. 7 TECNICHE DI LABORATORIO BIOMEDICO (ABILITANTE ALLA PROFESSIONE SANITARIA DI TECNICO DI LABORATORIO BIOMEDICO)

Pubblicazioni

Data Titolo Tipologia Scheda
2023 Prevalence and risk of new-onset diabetes mellitus after COVID-19: a systematic review and meta-analysis Articolo in rivista Vai
2022 Diabetes and cognitive decline Review essay (rassegna critica) Vai
2022 Influence of Nutritional Status and Physical Exercise on Immune Response in Metabolic Syndrome Review essay (rassegna critica) Vai
2021 The different daily distribution of proteins does not influence the variations in body composition in a sample of subjects undergoing a low-calorie Mediterranean-Type diet Articolo in rivista Vai
2021 Tropomyosin: A panallergen that causes a worldwide allergic problem Review essay (rassegna critica) Vai
2021 High plant-based diet and physical activity in women during menopausal transition Articolo in rivista Vai
2021 Glycated albumin for glycemic control in t2dm population: A multi-dimensional evaluation Articolo in rivista Vai
2020 Klotho and vitamin D in multiple sclerosis: an Italian study Articolo in rivista Vai
2020 If we eat soy, do we keep the beneficial effects of the Mediterranean diet? Articolo in rivista Vai
2020 Effects of Quality and Quantity of Protein Intake for Type 2 Diabetes Mellitus Prevention and Metabolic Control Articolo in rivista Vai
2020 Use of Troponin as a predictor for cardiovascular diseases in patients with type 2 Diabetes Mellitus Review essay (rassegna critica) Vai
2020 Diet high in protein-rich foods with structured sport activity may be useless to lose fat mass and maintain fat-free mass Articolo in rivista Vai
2020 Losing weight after menopause with minimal aerobic training and mediterranean diet Articolo in rivista Vai
2019 Vitamin D in malaria: more hypotheses than clues Articolo in rivista Vai
2019 Pazienti diabetici di tipo 2, non in terapia insulinica e albumina glicata: una valutazione multidimensionale Articolo in rivista Vai
2019 Endothelial function, adipokine serum levels and white matter hyperintesities in subjects with diabetic foot syndrome. Articolo in rivista Vai
2019 Non-skeletal activities of vitamin d: From physiology to brain pathology Articolo in rivista Vai
2019 Glycated albumin as a glycaemic marker in patients with advanced chronic kidney disease and anaemia: a preliminary report 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 Cerebrospinal Fluid Analysis in Multiple Sclerosis Diagnosis: An Update Review essay (rassegna critica) Vai
2019 Mid-regional pro-adrenomedullin predicts poor outcome in non-selected patients admitted to an intensive care unit Articolo in rivista Vai
2018 Glycated albumin is correlated to insulin resistance and β-cell secretory function in subjects at risk for developing diabetes Articolo in rivista Vai
2018 Association of CYP2R1 rs10766197 with MS risk and disease progression Articolo in rivista Vai
2018 A new role of CYP2R1 in Multiple Sclerosis Articolo in rivista Vai
2018 Use of saliva in alternative to serum sampling to monitor biomarkers modifications in professional soccer players Articolo in rivista Vai
2018 Diagnostic and prognostic value of H-FABP in acute coronary syndrome: Still evidence to bring Review essay (rassegna critica) Vai
2018 Clinical usefulness of Glycated Albumin in the diagnosis of diabetes: Results from an Italian study 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
2017 VDBP, CYP27B1, and 25-Hydroxyvitamin D Gene Polymorphism Analyses in a Group of Sicilian Multiple Sclerosis Patients Articolo in rivista Vai
2017 Acute troponin i increase in absence of obstructive coronary disease: A case of takotsubo syndrome Articolo in rivista Vai
2017 Establishing the upper reference limit of Galectin-3 in healthy blood donors Articolo in rivista Vai
2017 Galectin-3 in acute coronary syndrome Review essay (rassegna critica) Vai
2017 The cervical fracture as first symptom of multiple myeloma: A case report Articolo in rivista Vai
2017 Definition of the upper reference limit of glycated albumin in blood donors from Italy 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
2016 Short-term Changes in Gal 3 Circulating Levels After Acute Myocardial Infarction 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 Immune-inflammatory and metabolic effects of high dose furosemide plus hypertonic saline solution (HSS) treatment in cirrhotic subjects with refractory ascites Articolo in rivista Vai
2016 Authors’ reply Articolo in rivista 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 Utility of serum procalcitonin and C-reactive protein in severity assessment of community-acquired pneumonia in children Articolo in rivista Vai
2015 Procalcitonin and community-acquired pneumonia (CAP) in children 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 A risk score derived from the analysis of a cluster of 27 serum inflammatory cytokines to predict long term outcome in patients with acute myocardial infarction: A pilot study Articolo in rivista Vai
2015 Arterial stiffness indexes and serum cytokine levels in seronegative spondyloarthritis: relationships between stiffness markers and metabolic and immunoinflammatory variables Articolo in rivista Vai
2014 No effect of MTHFR C677T variant on homocysteine metabolism in Amiotrophic Lateral Sclerosis eedings Vai
2014 Vitamin K deficiency bleeding leading to a diagnosis of Crohn’s Disease Articolo in rivista Vai
2014 KRAS: one actor, many potential roles in diagnosis eedings Vai
2014 The implication of MBL deficient haplotypes in acute coronary syndrome Articolo in rivista Vai
2014 Molecular markers in acute coronary syndrome eedings Vai
2014 Effects of EPHX1 and CYP3A4 polymorphisms on carbamazepine metabolism in epileptic patients Articolo in rivista Vai
2014 Vitamin K Deficit leads to Chronic Inflammatory Bowel Disease Diagnosis: a case report eedings Vai
2014 MTHFR C677T allelic variant is not associated to plasma and cerebrospinal fluid homocysteine in amyotrophic lateral sclerosis eedings Vai
2013 Influence of CYP2C9 polymorphism on serum levels of phenobarbital metabolites eedings Vai
2013 Polimorfismo I/D del gene per l'enzima di conversione dell'angiotensina (ACE): gene della longevità o fattore di rischio nella patologia ipertensiva? Articolo in rivista Vai
2012 Activity of mannose-binding lectin in centenarians Articolo in rivista Vai
2012 Prothrombotic gene variants in AMI young women eedings Vai
2012 Methylenetetrahydrofolate reductase homozygosis and low-density lipoproteins in patients with genotype 1 chronic hepatitis C Articolo in rivista Vai
2012 Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. Articolo in rivista Vai
2012 Evaluation of the EPHX1 polymorphism on serum levels of 10, 11- eposside carbamazepine eedings Vai
2012 Fetuin-A serum levels are not correlated to kidney function in long-lived subjects Articolo in rivista Vai
2011 Separazione della beta-N-metilammino-L-alanina (BMAA) in campioni di liquor cefalorachidiano mediante HPLC con rilevazione fluorimetrica eedings Vai
2011 Fetuin-A in elderly: effect of genotype on serum levels Capitolo o Saggio Vai
2011 SEARCH OF MUTATIONS IN CFTR GENE AND IN GENES ENCODING CFTR INTERACTORS IN PATIENTS BEARING ATYPICAL CISTIC FIBROSIS Capitolo o Saggio Vai
2011 APOE and longevity: study of a population of Sardinian Centenarians Capitolo o Saggio Vai
2011 Extensive molecular analysis of patients bearing CFTR-related disorders. Articolo in rivista Vai
2010 Clinical utilization of natriuretic peptide determination in acute congestive heart failure Articolo in rivista Vai
2010 Hyperhomocysteinemia and cardiovascular risk: effect of vitamin supplementation in risk reduction Articolo in rivista Vai
2010 Varianti alleliche del gene per la lecitina legante il mannosio (MBL): un vantaggio o uno svantaggio per la longevità? Articolo in rivista Vai
2010 B-type natriuretic peptides and thyroid disease Articolo in rivista Vai
2010 Frequiencies of PAI-1 4G/5G polymorphism in Elderly eedings Vai
2010 APO E allelic variants in healthy elderly people eedings Vai
2010 Effect of vitamin supplementation on hyperhomocysteinemia and cardiovascular risk reduction Articolo in rivista Vai
2010 Fetuin-A and CD40L plasma levels in acute ischemic stroke: differences in relation to TOAST subtype and correlation with clinical and laboratory variables Articolo in rivista Vai
2010 ADIPONECTIN, RESISTIN AND IL-6 PLASMA LEVELS IN SUBJECTS WITH DIABETIC FOOT AND POSSIBLE CORRELATION WITH CLINICAL VARIABLES AND CARDIOVASCULAR CO-MORBIDITY Articolo in rivista Vai
2009 Fetuin-A, renal function and cardiovascular disease in elderly subjects eedings Vai
2008 Clinical applications of Proton Spectroscopy in the study of neurodegenerative disease eedings Vai
2008 Low serum Fetuin A levels and cardiovascular events in End-Stage Renal Disease (ESRD) patients. Articolo in rivista Vai
2008 Changes in serum Fetuin A and inflammatory markers levels in end stage renal disease (ESRD),effect of a single session haemodialysis Articolo in rivista Vai
2008 Therapeutical approach on plasma homocysteine and cardiovascular risk reduction Articolo in rivista Vai
2008 Comparison of two assays for serum homocysteine measurement eedings Vai
2008 Plasminogen Activator Inhibitor-1 -675 4G/5G and Methylenetetrahydrofolate reductase gene variants in young acute myocardial infarction and juvenile ischemic stroke Articolo in rivista Vai
2008 CSF homocysteine levels in Amyotrophic Lateral Sclerosis eedings Vai
2008 Molecular diagnostics of thrombophilia eedings Vai
2008 Genetic variants beta-fibrinogen gene, especially G-455-A polymorphism, in patients with thromboembolic disease. eedings Vai
2008 Mutation in beta-fibrinogen gene (C148T) is important risk factor in patients affected by thromboembolic disease. eedings Vai
2008 Hyperhomocysteinemia in patients with cognitive impairment Articolo in rivista Vai
2008 CSF HOMOCYSTEINE LEVELS IN AMYOTROPHC LATERAL SCLEROSIS eedings Vai
2008 Buerger's Disease and Hyperhomocysteinemia: is there a relationship? Articolo in rivista Vai
2008 Oxidative damage markers eedings Vai
2007 Changes in serum fetuin-A and inflammatory markers levels in end stage renal disease (ESRD): effect of a single session haemodialysis. eedings Vai
2007 The risk of cardiovascular events is reduced by lowering hyperhomocysteinemia short term B vitamins therapy eedings Vai
2007 GERD patients: a risk group for xerostomia and oral lesions? A case-control syudy eedings Vai
2007 Factor V Leiden, Prothrombin G20210A mutations are risk factors for deep vein thrombosis eedings Vai
2007 Effects of polymorphism of Methionine Synthase Reductase on total plasma homocysteine in Sicilian populations eedings Vai
2007 Hyperhomocysteinemia and methylenetetrahydrofolare reductase 677C→T and 1298A→C mutations in patients with venous thromboembolic disease eedings Vai
2007 Mutations in Factor V Leiden (G1691A) and Prothrombin (G2021A) genes are important risk factors for venous thromboembolism eedings Vai
2007 Association between homocysteinemia and Metabolic Syndrome in patients with cardiovascular disease Articolo in rivista Vai
2007 Vitamin E and vitamin A plasma levels in patients with Mild Cognitive Impairent (MCI) eedings Vai
2007 Molecular analysis of genes encoding CFTR interactors of SLC26 family in CF patients: preliminary results eedings Vai
2007 Apo E polymorphism as risk factor for cardiovascular diseases in Sicilian subjects. eedings Vai
2006 The Homocysteine System Articolo in rivista Vai
2006 Homocysteine and MTHFR gene polimorphysms in patients with venous tromboembolic disease eedings Vai
2006 Prevalence and association of the Factor V Leiden and Prothrombin G20210A in healthy subjects and patients with venous tromboembolism eedings Vai
2006 Low Fetuin-A plasma levels are associated with the presence of carotid plaques in patients on dialysis. eedings Vai
2005 Evaluation of plasma homocysteine levels and metabolic sindrome in patients with cardiovascular disease eedings Vai
2005 Plasma homocysteine levels in patients with metabolic syndrome eedings Vai
2005 Low serum fetuin-A in renal failure patients on Hemodialisis eedings Vai
2005 Serum Fetuin A concentration in patients on haemodialysis eedings Vai
2005 Nutrienti nella prevenzione dello Stress Ossidativo Articolo in rivista Vai
2005 Metabolic sindrome and increased risk for cardiovascular disease eedings Vai
2005 Effect of MTHFR polymorphism on homocysteine level after Methionine loading in thromboembolic patients. eedings Vai
2005 Biochimica clinica dello stress ossidativo Articolo in rivista Vai
2005 Serum Fetuin A concentration in patients on Hemodialysis eedings Vai
2005 Low serum Fetuin A levels in renal failure patients on haemodialysis eedings Vai
2004 Molecular analysis of the APP gene overexpression and his relationship with early onset of Alzheimer Dementia in young adults with Down Syndrome eedings Vai
2004 Curva da carico orale di metionina nella valutazione di pazienti affetti da patologia trombotica eedings Vai
2004 Mutation analysis of the ΔR 608 mutation causing Niemann-Pick disease type B from blood spot cards in sicilian people eedings Vai
2004 Dangerous ratio modification of plasma and erythrocyte S-adenosylmethionine/S-adenosylhomocysteine in cardiovascular disease Altro Vai