2024 |
A Heuristic Approach to Analysis of the Genetic Susceptibility Profile in Patients Affected by Airway Allergies |
Articolo in rivista |
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2024 |
Diagnostic Accuracy of Lipid Transfer Proteins (LTPs) Specific IgE Assay in Food Allergy: A Systematic Review |
Review essay (rassegna critica) |
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2023 |
Prevalence and risk of new-onset diabetes mellitus after COVID-19: a systematic review and meta-analysis |
Articolo in rivista |
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2022 |
Influence of Nutritional Status and Physical Exercise on Immune Response in Metabolic Syndrome |
Review essay (rassegna critica) |
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2022 |
High plant-based diet and physical activity in women during menopausal transition |
Articolo in rivista |
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2022 |
Diabetes and cognitive decline |
Review essay (rassegna critica) |
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2021 |
Tropomyosin: A panallergen that causes a worldwide allergic problem |
Review essay (rassegna critica) |
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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 |
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2021 |
Glycated albumin for glycemic control in t2dm population: A multi-dimensional evaluation |
Articolo in rivista |
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2020 |
Klotho and vitamin D in multiple sclerosis: an Italian study |
Articolo in rivista |
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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 |
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2020 |
Losing weight after menopause with minimal aerobic training and mediterranean diet |
Articolo in rivista |
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2020 |
Use of Troponin as a predictor for cardiovascular diseases in patients with type 2 Diabetes Mellitus |
Review essay (rassegna critica) |
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2020 |
Effects of Quality and Quantity of Protein Intake for Type 2 Diabetes Mellitus Prevention and Metabolic Control |
Articolo in rivista |
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2020 |
If we eat soy, do we keep the beneficial effects of the Mediterranean diet? |
Articolo in rivista |
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2019 |
Mid-regional pro-adrenomedullin predicts poor outcome in non-selected patients admitted to an intensive care unit |
Articolo in rivista |
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2019 |
Vitamin D in malaria: more hypotheses than clues |
Articolo in rivista |
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2019 |
Glycated albumin as a glycaemic marker in patients with advanced chronic kidney disease and anaemia: a preliminary report |
Articolo in rivista |
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2019 |
Pazienti diabetici di tipo 2, non in terapia insulinica e albumina glicata: una valutazione multidimensionale |
Articolo in rivista |
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2019 |
Non-skeletal activities of vitamin d: From physiology to brain pathology |
Articolo in rivista |
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2019 |
Cerebrospinal Fluid Analysis in Multiple Sclerosis Diagnosis: An Update |
Review essay (rassegna critica) |
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2019 |
Endothelial function, adipokine serum levels and white matter hyperintesities in subjects with diabetic foot syndrome. |
Articolo in rivista |
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2019 |
Establishing the 99th percentile for high sensitivity cardiac troponin i in healthy blood donors from southern italy |
Articolo in rivista |
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2018 |
Association of CYP2R1 rs10766197 with MS risk and disease progression |
Articolo in rivista |
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2018 |
Clinical usefulness of Glycated Albumin in the diagnosis of diabetes: Results from an Italian study |
Articolo in rivista |
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2018 |
Use of saliva in alternative to serum sampling to monitor biomarkers modifications in professional soccer players |
Articolo in rivista |
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2018 |
Diagnostic and prognostic value of H-FABP in acute coronary syndrome: Still evidence to bring |
Review essay (rassegna critica) |
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2018 |
A new role of CYP2R1 in Multiple Sclerosis |
Articolo in rivista |
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2018 |
Glycated albumin is correlated to insulin resistance and β-cell secretory function in subjects at risk for developing diabetes |
Articolo in rivista |
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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 |
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2017 |
VDBP, CYP27B1, and 25-Hydroxyvitamin D Gene Polymorphism Analyses in a Group of Sicilian Multiple Sclerosis Patients |
Articolo in rivista |
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2017 |
Galectin-3 in acute coronary syndrome |
Review essay (rassegna critica) |
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2017 |
Acute troponin i increase in absence of obstructive coronary disease: A case of takotsubo syndrome |
Articolo in rivista |
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2017 |
Definition of the upper reference limit of glycated albumin in blood donors from Italy |
Articolo in rivista |
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2017 |
Establishing the upper reference limit of Galectin-3 in healthy blood donors |
Articolo in rivista |
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2017 |
The cervical fracture as first symptom of multiple myeloma: A case report |
Articolo in rivista |
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2016 |
Utility of serum procalcitonin and C-reactive protein in severity assessment of community-acquired pneumonia in children |
Articolo in rivista |
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2016 |
Vitamin D receptor polymorphisms and 25-hydroxyvitamin D in a group of Sicilian multiple sclerosis patients |
Articolo in rivista |
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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 |
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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 |
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2016 |
Fetuin-A is Associated to Serum Calcium and AHSG T256S Genotype but Not to Coronary Artery Calcification |
Articolo in rivista |
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2016 |
Authors’ reply |
Articolo in rivista |
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2016 |
Short-term Changes in Gal 3 Circulating Levels After Acute Myocardial Infarction |
Articolo in rivista |
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2015 |
Procalcitonin and community-acquired pneumonia (CAP) in children |
Articolo in rivista |
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2015 |
Arterial stiffness indexes and serum cytokine levels in seronegative spondyloarthritis: relationships between stiffness markers and metabolic and immunoinflammatory variables |
Articolo in rivista |
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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 |
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2015 |
MTHFR C677T allelic variant is not associated to plasma and cerebrospinal fluid homocysteine in Amyotrophic Lateral Sclerosis |
Articolo in rivista |
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2014 |
No effect of MTHFR C677T variant on homocysteine metabolism in Amiotrophic Lateral Sclerosis |
Proceedings |
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2014 |
Vitamin K deficiency bleeding leading to a diagnosis of Crohn’s Disease |
Articolo in rivista |
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2014 |
KRAS: one actor, many potential roles in diagnosis |
Proceedings |
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2014 |
The implication of MBL deficient haplotypes in acute coronary syndrome |
Articolo in rivista |
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2014 |
Molecular markers in acute coronary syndrome |
Proceedings |
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2014 |
Effects of EPHX1 and CYP3A4 polymorphisms on carbamazepine metabolism in epileptic patients |
Articolo in rivista |
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2014 |
Vitamin K Deficit leads to Chronic Inflammatory Bowel Disease Diagnosis: a case report |
Proceedings |
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2014 |
MTHFR C677T allelic variant is not associated to plasma and cerebrospinal fluid homocysteine in amyotrophic lateral sclerosis |
Proceedings |
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2013 |
Influence of CYP2C9 polymorphism on serum levels of phenobarbital metabolites |
Proceedings |
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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 |
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2012 |
Activity of mannose-binding lectin in centenarians |
Articolo in rivista |
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2012 |
Prothrombotic gene variants in AMI young women |
Proceedings |
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2012 |
Methylenetetrahydrofolate reductase homozygosis
and low-density lipoproteins in patients with genotype 1 chronic hepatitis C |
Articolo in rivista |
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2012 |
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. |
Articolo in rivista |
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2012 |
Evaluation of the EPHX1 polymorphism on serum levels of 10, 11- eposside carbamazepine |
Proceedings |
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2012 |
Fetuin-A serum levels are not correlated to kidney function in long-lived subjects |
Articolo in rivista |
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2011 |
Separazione della beta-N-metilammino-L-alanina (BMAA) in campioni di liquor cefalorachidiano mediante HPLC con rilevazione fluorimetrica |
Proceedings |
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2011 |
Fetuin-A in elderly: effect of genotype on serum levels |
Capitolo o Saggio |
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2011 |
SEARCH OF MUTATIONS IN CFTR GENE AND IN GENES ENCODING CFTR INTERACTORS IN PATIENTS BEARING ATYPICAL CISTIC FIBROSIS |
Capitolo o Saggio |
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2011 |
APOE and longevity: study of a population of Sardinian Centenarians |
Capitolo o Saggio |
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2011 |
Extensive molecular analysis of patients bearing CFTR-related disorders. |
Articolo in rivista |
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2010 |
Clinical utilization of natriuretic peptide determination in acute congestive heart failure |
Articolo in rivista |
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2010 |
Hyperhomocysteinemia and cardiovascular risk: effect of vitamin supplementation in risk reduction |
Articolo in rivista |
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2010 |
Varianti alleliche del gene per la lecitina legante il mannosio (MBL): un vantaggio o uno svantaggio per la longevità? |
Articolo in rivista |
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2010 |
B-type natriuretic peptides and thyroid disease |
Articolo in rivista |
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2010 |
Frequiencies of PAI-1 4G/5G polymorphism in Elderly |
Proceedings |
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2010 |
APO E allelic variants in healthy elderly people |
Proceedings |
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2010 |
Effect of vitamin supplementation on hyperhomocysteinemia and cardiovascular risk reduction |
Articolo in rivista |
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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 |
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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 |
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2009 |
Fetuin-A, renal function and cardiovascular disease in elderly subjects |
Proceedings |
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2008 |
Clinical applications of Proton Spectroscopy in the study of neurodegenerative disease |
Proceedings |
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2008 |
Low serum Fetuin A levels and cardiovascular events in End-Stage Renal Disease (ESRD) patients. |
Articolo in rivista |
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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 |
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2008 |
Therapeutical approach on plasma homocysteine and cardiovascular risk reduction |
Articolo in rivista |
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2008 |
Comparison of two assays for serum homocysteine measurement |
Proceedings |
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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 |
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2008 |
Oxidative damage markers |
Proceedings |
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2008 |
Genetic variants beta-fibrinogen gene, especially G-455-A polymorphism, in patients with thromboembolic disease. |
Proceedings |
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2008 |
Molecular diagnostics of thrombophilia |
Proceedings |
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2008 |
Mutation in beta-fibrinogen gene (C148T) is important risk factor in patients affected by thromboembolic disease. |
Proceedings |
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2008 |
CSF HOMOCYSTEINE LEVELS IN AMYOTROPHC LATERAL SCLEROSIS |
Proceedings |
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2008 |
Hyperhomocysteinemia in patients with cognitive impairment |
Articolo in rivista |
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2008 |
CSF homocysteine levels in Amyotrophic Lateral Sclerosis |
Proceedings |
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2008 |
Buerger's Disease and Hyperhomocysteinemia: is there a relationship? |
Articolo in rivista |
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2007 |
Apo E polymorphism as risk factor for cardiovascular diseases in Sicilian subjects. |
Proceedings |
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2007 |
Changes in serum fetuin-A and inflammatory markers levels in end stage renal disease (ESRD): effect of a single session haemodialysis. |
Proceedings |
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2007 |
The risk of cardiovascular events is reduced by lowering hyperhomocysteinemia short term B vitamins therapy |
Proceedings |
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2007 |
Molecular analysis of genes encoding CFTR interactors of SLC26 family in CF patients: preliminary results |
Proceedings |
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2007 |
Hyperhomocysteinemia and methylenetetrahydrofolare reductase 677C→T and 1298A→C mutations in patients with venous thromboembolic disease |
Proceedings |
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2007 |
Vitamin E and vitamin A plasma levels in patients with Mild Cognitive Impairent (MCI) |
Proceedings |
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2007 |
GERD patients: a risk group for xerostomia and oral lesions? A case-control syudy |
Proceedings |
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2007 |
Association between homocysteinemia and Metabolic Syndrome in patients with cardiovascular disease |
Articolo in rivista |
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2007 |
Mutations in Factor V Leiden (G1691A) and Prothrombin (G2021A) genes are important risk factors for venous thromboembolism |
Proceedings |
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2007 |
Factor V Leiden, Prothrombin G20210A mutations are risk factors for deep vein thrombosis |
Proceedings |
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2007 |
Effects of polymorphism of Methionine Synthase Reductase on total plasma homocysteine in Sicilian populations |
Proceedings |
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2006 |
The Homocysteine System |
Articolo in rivista |
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2006 |
Low Fetuin-A plasma levels are associated with the presence of carotid plaques in patients on dialysis. |
Proceedings |
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2006 |
Prevalence and association of the Factor V Leiden and Prothrombin G20210A in healthy subjects and patients with venous tromboembolism |
Proceedings |
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2006 |
Homocysteine and MTHFR gene polimorphysms in patients with venous tromboembolic disease |
Proceedings |
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2005 |
Effect of MTHFR polymorphism on homocysteine level after Methionine loading in thromboembolic patients. |
Proceedings |
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2005 |
Evaluation of plasma homocysteine levels and metabolic sindrome in patients with cardiovascular disease |
Proceedings |
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2005 |
Serum Fetuin A concentration in patients on Hemodialysis |
Proceedings |
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2005 |
Low serum Fetuin A levels in renal failure patients on haemodialysis |
Proceedings |
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2005 |
Serum Fetuin A concentration in patients on haemodialysis |
Proceedings |
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2005 |
Metabolic sindrome and increased risk for cardiovascular disease |
Proceedings |
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2005 |
Low serum fetuin-A in renal failure patients on Hemodialisis |
Proceedings |
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2005 |
Plasma homocysteine levels in patients with metabolic syndrome |
Proceedings |
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2005 |
Nutrienti nella prevenzione dello Stress Ossidativo |
Articolo in rivista |
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2005 |
Biochimica clinica dello stress ossidativo |
Articolo in rivista |
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2004 |
Curva da carico orale di metionina nella valutazione di pazienti affetti da patologia trombotica |
Proceedings |
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2004 |
Mutation analysis of the ΔR 608 mutation causing Niemann-Pick disease type B from blood spot cards in sicilian people |
Proceedings |
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2004 |
Dangerous ratio modification of plasma and erythrocyte S-adenosylmethionine/S-adenosylhomocysteine in cardiovascular disease |
Altro |
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2004 |
Molecular analysis of the APP gene overexpression and his relationship with early onset of Alzheimer Dementia in young adults with Down Syndrome |
Proceedings |
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