Research Topics
Genomes and Genes
Species | Oliviero OlivieriSummaryAffiliation: University of Verona Country: Italy Publications
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Detail Information
Publications
Cystatin C versus creatinine in renovascular diseaseOliviero Olivieri
Department of Clinical and Experimental Medicine, Unit of Internal Medicine, University of Verona, 37134 Verona, Italy
Clin Chem 48:2256-9. 2002
Urinary cortisol to cortisone metabolites ratio in prednisone-treated and spontaneously hypertensive patientsOliviero Olivieri
Unit of Internal Medicine, Department of Clinical and Experimental Medicine, University of Verona, Italy
J Hypertens 26:486-93. 2008....
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery diseaseOliviero Olivieri
Unit of Internal Medicine, Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
J Lipid Res 44:2374-81. 2003..6% vs. 34.8%, P < 0.05). In conclusion, apoC-III-rich lipoprotein metabolism and the APOC3 polymorphism have relevant impacts on the CAD risk of MS patents...
Urinary prostasin: a candidate marker of epithelial sodium channel activation in humansOliviero Olivieri
Department of Clinical and Experimental Medicine, University of Verona, Italy
Hypertension 46:683-8. 2005....
ApoC-III gene polymorphisms and risk of coronary artery diseaseOliviero Olivieri
Unit of Internal Medicine, Institute of Clinical Chemistry, University of Verona, Verona, Italy
J Lipid Res 43:1450-7. 2002..5 and 2.18 for unadjusted and adjusted models, respectively) suggesting that it represents an independent genetic susceptibility factor for CAD...
Aldosterone to Renin ratio in a primary care setting: the Bussolengo studyOliviero Olivieri
Dipartimento Medicina Clinica e Sperimentale, Cattedra di Medicina Interna, Universita di Verona, Policlinico Borgo Roma, 37134 Verona, Italy
J Clin Endocrinol Metab 89:4221-6. 2004..As an elevated AARR is frequent in the general hypertensive population, screening should not be limited to the patients referred to specialist units...
Apolipoprotein C-III predicts cardiovascular mortality in severe coronary artery disease and is associated with an enhanced plasma thrombin generationO Olivieri
Department of Clinical and Experimental Medicine, Unit of Internal Medicine, University of Verona, Verona, Italy
J Thromb Haemost 8:463-71. 2010..Apolipopoprotein C-III (apo C-III) plays a pivotal role in controlling plasma triglyceride (TG) and contributes to the atherogenic properties of TG-rich lipoproteins...
ApoE epsilon2/epsilon3/epsilon4 polymorphism, ApoC-III/ApoE ratio and metabolic syndromeO Olivieri
Unit of Internal Medicine, Department of Clinical and Experimental Medicine, Cattedra di Medicina Interna, University of Verona, Policlinico Borgo Roma, 37134, Verona, Italy
Clin Exp Med 7:164-72. 2007..Carriers of the unfavourable E4 allele present the highest ApoCIII/ApoE ratio and are twofold more frequent among individuals affected by MetSyn...
Homocysteine and atheromatous renal artery stenosisO Olivieri
Department of Clinical and Experimental Medicine, University of Verona, Italy
Clin Exp Med 1:211-8. 2001..Folate supplementation might be useful in the management of overall vascular risk of these patients...
Menopause not aldosterone-to-renin ratio predicts blood pressure response to a mineralocorticoid receptor antagonist in primary care hypertensive patientsOliviero Olivieri
Unit of Internal Medicine, Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Am J Hypertens 21:976-82. 2008..We therefore designed an interventional study to ascertain whether primary care hypertensive patients with an elevated ARR presented a superior response to MRA treatment than subjects with normal ratio...
Different impact of deletion polymorphism of gene on the risk of renal and coronary artery diseaseOliviero Olivieri
Department of Clinical and Experimental Medicine, Chair of Internal Medicine, University of Verona, Policlinico Borgo Roma, 37134 Verona, Italy
J Hypertens 20:37-43. 2002....
Apolipoprotein C-III, n-3 polyunsaturated fatty acids, and "insulin-resistant" T-455C APOC3 gene polymorphism in heart disease patients: example of gene-diet interactionOliviero Olivieri
Unit of Internal Medicine, Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Clin Chem 51:360-7. 2005..The T-455C polymorphism in the insulin-responsive element of the APOC3 gene influences TG and apo C-III concentrations. Long-chain n-3 polyunsaturated fatty acids (PUFAs) contained in fish have well-known apo C-III-lowering properties...
The -1131 T>C and S19W APOA5 gene polymorphisms are associated with high levels of triglycerides and apolipoprotein C-III, but not with coronary artery disease: an angiographic studyNicola Martinelli
University of Verona, Department of Clinical and Experimental Medicine, Italy
Atherosclerosis 191:409-17. 2007..Different genotypes, i.e., APOA5 and APOC3 variants, may lead to similar biochemical phenotypes, namely hypertriglyceridemia, but to contrasting clinical phenotypes such as the presence of angiographically proven CAD...
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosisNicola Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
PLoS ONE 3:e1523. 2008..The aim of this study was to evaluate the combined effect of ten common prothrombotic polymorphisms as a determinant of MI...
Hyperhomocysteinemia and mortality after coronary artery bypass graftingDomenico Girelli
Department of Clinical and Experimental Medicine, University of Verona, Italy
PLoS ONE 1:e83. 2006..No previous study specifically has addressed the relationship between HHcy and mortality after coronary artery bypass grafting (CABG) surgery. The aim of this study is to evaluate the prognostic impact of HHcy after CABG surgery...
FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery diseaseNicola Martinelli
Department of Clinical and Experimental Medicine and the Section of Biology and Genetics, University of Verona, Verona, Italy
Am J Clin Nutr 88:941-9. 2008..Single-nucleotide polymorphisms (SNPs) in FADS1 and FADS2 have been associated with different concentrations of AA and LA, and those associations have possible functional consequences for desaturase activity...
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based studyDomenico Girelli
Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Eur J Hum Genet 15:959-66. 2007..Our angiography-based study suggests a possible modest role of ALOX5AP in the development of the atheroma rather than in its late thrombotic complications such as MI...
Primary hyperaldosteronism: a frequent cause of residual hypertension after successful endovascular treatment of renal artery diseaseFrancesca Pizzolo
Unit of Internal Medicine, Department of Clinical and Experimental Medicine, University of Verona, Italy
J Hypertens 23:2041-7. 2005..CONCLUSIONS: Primary hyperaldosteronism is a frequently neglected cause of residual hypertension despite technically successful endovascular treatment of renal artery disease...
Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery diseaseSimonetta Friso
Department of Medicine, University of Verona School of Medicine, Verona, Italy
J Med Genet 49:192-9. 2012..Transcriptional regulation of F7 by epigenetic features is, however, still unknown as is the inter-relationship of genetic and epigenetic modifications at the promoter site...
Gene sequence variations of the platelet P2Y12 receptor are associated with coronary artery diseaseUgo Cavallari
Department of Mother and Child and of Biology Genetics, Section of Biology and Genetics, University of Verona, Verona, Italy
BMC Med Genet 8:59. 2007..No data are available on its association with coronary artery disease (CAD)...
The interaction between MTHFR 677 C-->T genotype and folate status is a determinant of coronary atherosclerosis riskDomenico Girelli
Department of Clinical and Experimental Medicine, Institute of Biology and Genetics, University of Verona, Policlinico G B Rossi, 37134 Verona, Italy
J Nutr 133:1281-5. 2003..8, 95% CI, 1.03-3.15). A gene-nutrient interaction that defines a higher risk for CAD is determined by folate levels below specific thresholds, which differ depending on the MTHFR 677 C-->T genotype...
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control studyNicola Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
BMC Med Genet 10:41. 2009....
Effects of female sex hormones and contraceptive pill on the diagnostic work-up for primary aldosteronismFrancesca Pizzolo
Department of Clinical and Experimental Medicine, Section of Internal Medicine, Universita di Verona, Verona, Italy
J Hypertens 28:135-42. 2010....
Hepcidin is not useful as a biomarker for iron needs in haemodialysis patients on maintenance erythropoiesis-stimulating agentsNicola Tessitore
Hemodialysis Unit Ospedale Policlinico, Division of Nephrology, University of Verona, Verona, Italy
Nephrol Dial Transplant 25:3996-4002. 2010..It has been suggested that hepcidin may be useful as a tool for managing iron therapy in haemodialysis (HD) patients on erythropoiesis-stimulating agents (ESA)...
Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profileNicola Martinelli
Department of Medicine, University of Verona, Verona, Italy
Blood 116:5688-97. 2010..67 with 95% confidence interval, 1.10-2.54). Haplotype analysis confirmed such results. Our data suggest that polymorphisms at LDLR locus modulate FVIII:c levels and may be associated with CAD risk independently from plasma lipids...
Epigenetic control of 11 beta-hydroxysteroid dehydrogenase 2 gene promoter is related to human hypertensionSimonetta Friso
Department of Clinical and Experimental Medicine, University of Verona School of Medicine, Verona, Italy
Atherosclerosis 199:323-7. 2008..Little is known, however, of human HSD11B2 epigenetic control and its relationship with the onset of hypertension...
The MTHFR 1298A>C polymorphism and genomic DNA methylation in human lymphocytesSimonetta Friso
Department of Clinical and Experimental Medicine, University of Verona, Policlinico Giambattista Rossi, Piazza Ludovico Antonio Scuro, 10, 37134 Verona, Italy
Cancer Epidemiol Biomarkers Prev 14:938-43. 2005..Further mechanistic studies are warranted to investigate how single polymorphisms as well as MTHFR combined genotypes exert their effect on cancer susceptibility...
Serum levels of the hepcidin-20 isoform in a large general population: the Val Borbera studyNatascia Campostrini
Department of Medicine, Section of Internal Medicine, University of Verona, Italy
J Proteomics 76:28-35. 2012..This article is part of a Special Issue entitled: Integrated omics...
Low plasma vitamin B-6 concentrations and modulation of coronary artery disease riskSimonetta Friso
Department of Clinical and Experimental Medicine, University of Verona School of Medicine, Verona, Italy
Am J Clin Nutr 79:992-8. 2004..Both low PLP and elevated inflammatory markers, such as high-sensitivity CRP (hs-CRP) and fibrinogen, are related to higher risk of coronary artery disease (CAD)...
Prevalence of body iron excess in the metabolic syndromeClaudia Bozzini
Department of Clinical and Experimental Medicine, University of Verona, Policlinico G.B. Rossi, 37134 Verona, Italy
Diabetes Care 28:2061-3. 2005
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularizationFrancesca Pizzolo
Section of Internal Medicine, Department of Clinical and Experimental Medicine, University of Verona, Policlinico Borgo Roma, 37134 Verona, Italy
J Vasc Surg 39:140-7. 2004....
Detection of a large deletion in the P-selectin (SELP) geneAlessandra Pasquali
Department of Mother and Child, and Biology Genetics, University of Verona, Strada Le Grazie 8, Verona, Italy
Mol Cell Probes 24:161-5. 2010..Re-genotyping of 1023 apparent homozygotes indicated an overall allele frequency of 0.27%. The inclusion of this allelic variant in genetic association studies will avoid genotyping errors and marginally improve the sensitivity...
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery diseaseElisabetta Trabetti
Department of Mother and Child and of Biology Genetics, Section of Biology and Genetics, University of Verona, Verona, Italy
Eur J Hum Genet 14:127-30. 2006..Even if the OLR1 genotype frequency distribution data in CAD or AMI subjects here reported do not fully confirm the positive results of some other association studies, an association with a marker of CAD severity was observed...
Novel serum paraoxonase activity assays are associated with coronary artery diseaseNicola Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Clin Chem Lab Med 47:432-40. 2009..The aim of this study was to evaluate for the first time TBBLase and DEPCyMCase activity in patients with coronary artery disease (CAD)...
Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphismNicola Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Italy
Blood Coagul Fibrinolysis 18:125-9. 2007..The report concomitantly addresses the relationship between factor V and factor VIII levels and supports the hypothesis of a mild prothrombotic role of FVHR2 by means of increased factor VIII levels...
Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosisClaudia Bozzini
Department of Clinical and Experimental Medicine, University of Verona, Policlinico G B Rossi, 37134 Verona, Italy
Thromb Haemost 92:541-9. 2004..This study highlights a "within-gene" interaction, and the need to explore polymorphisms in candidate gene(s) in detail...
Folic acid effects on s-adenosylmethionine, s-adenosylhomocysteine, and DNA methylation in patients with intermediate hyperhomocysteinemiaFrancesca Pizzolo
Department of Medicine, University of Verona School of Medicine, Verona, Italy
J Am Coll Nutr 30:11-8. 2011..The purpose of this study was to investigate the effects of FA supplementation on AdoMet, AdoHcy, and genomic DNA methylation in hyperhomocysteinemic subjects without end-stage renal disease...
Low levels of serum paraoxonase activities are characteristic of metabolic syndrome and may influence the metabolic-syndrome-related risk of coronary artery diseaseNicola Martinelli
Department of Medicine, University of Verona, Policlinico G B Rossi, Italy
Exp Diabetes Res 2012:231502. 2012..45 with 95% CI 0.47-4.46). Our results suggest that low PON1 concentrations are typical in MS and may modulate the MS-related risk of CAD...
Biochemical and genetic markers of iron status and the risk of coronary artery disease: an angiography-based studyClaudia Bozzini
Department of Clinical and Experimental Medicine, University of Verona, 37134 Verona, Italy
Clin Chem 48:622-8. 2002..Iron may promote coronary atherosclerotic disease (CAD) by increasing lipid peroxidation. Studies on biochemical or genetic markers of body iron stores as risk factors for CAD have yielded conflicting results...
SNPs of the FADS gene cluster are associated with polyunsaturated fatty acids in a cohort of patients with cardiovascular diseaseGiovanni Malerba
Department of Mother and Child, and Biology Genetics, Section of Biology and Genetics, University of Verona, Verona, Italy
Lipids 43:289-99. 2008....
Paraoxonases: ancient substrate hunters and their evolving role in ischemic heart diseaseNicola Martinelli
Department of Medicine, Section of Internal Medicine, University of Verona, Verona, Italy
Adv Clin Chem 59:65-100. 2013..In this review, we examine the biochemical pathways impacted by these unique enzymes and investigate the potential use of PON as diagnostic tools and their impact on development of future therapeutic strategies...
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer riskSimonetta Friso
Corresponding Author Simonetta Friso, Department of Medicine, University of Verona School of Medicine, Policlinico G B Rossi, P le L A Scuro, 10, 37134 Verona, Italy
Cancer Epidemiol Biomarkers Prev 22:348-55. 2013..Whether methylation measured in peripheral blood mononuclear cells (PBMCs) DNA is a clinically reliable biomarker for early detection or cancer risk assessment is to be established...
Measurement of urinary hepcidin levels by SELDI-TOF-MS in HFE-hemochromatosisClaudia Bozzini
Department of Clinical and Experimental Medicine, University of Verona, Policlinico G B Rossi, 37134 Verona, Italy
Blood Cells Mol Dis 40:347-52. 2008..This study measured urinary hepcidin levels by SELDI-TOF-MS in a large group of HH patients at diagnosis and during treatment, including both C282Y homozygous and C282Y/H63D compound heterozygotes...
Evaluation of hepcidin isoforms in hemodialysis patients by a proteomic approach based on SELDI-TOF MSNatascia Campostrini
Department of Medicine, University of Verona, 37134 Verona, Italy
J Biomed Biotechnol 2010:329646. 2010..Measurement of hepcidin isoforms through MS-based techniques can be a useful tool for better understanding of their biological role in hemodialysis patients and other clinical conditions...
Murine macrophages response to ironRita Polati
University of Verona, Department of Biotechnology, Strada Le Grazie 15, 37134 Verona, Italy
J Proteomics 76:10-27. 2012..This article is part of a Special Issue entitled: Integrated omics...
Laboratory diagnosis of primary aldosteronism, and drospirenone-ethinylestradiol therapyFrancesca Pizzolo
Unit of Internal Medicine, Department of Clinical and Experimental Medicine, University of Verona, Policlinico Borgo Roma, Verona, Italy
Am J Hypertens 20:1334-7. 2007..Our objective was to evaluate the possible interference of a new progestin with antimineralocorticoid activity (drospirenone) on the determination of ARR and the diagnosis of primary aldosteronism...
G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery diseaseC Russo
Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Circulation 103:2436-40. 2001..The role of this common polymorphism, as well as that of prothrombin levels, in determining the risk of arterial disease is still somewhat controversial...
Thrombosis and sickle cell diseaseLucia De Franceschi
Department of Medicine, University of Verona, Verona, Italy
Semin Thromb Hemost 37:226-36. 2011..We also review the available studies on the therapeutic approaches in clinical management of hypercoagulability in SCD...
Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 geneDomenico Girelli
Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Gastroenterology 122:1295-302. 2002..Here we report data from a family carrying a new mutation of the transferrin receptor 2 gene...
Genetic architecture of coronary artery disease in the genome-wide era: implications for the emerging "golden dozen" lociDomenico Girelli
Department of Clinical and Experimental Medicine, Section of Internal Medicine, University of Verona, Italy
Semin Thromb Hemost 35:671-82. 2009..Although these genetic variants have little or no current predictive value of at the level of individual patients, they have the potential to disclose novel biological mechanisms involved in the pathophysiology of CAD/MI...
Female urinary proteomics: New insight into exogenous and physiological hormone-dependent changesAnnalisa Castagna
Department of Medicine, Unit of Internal Medicine, University of Verona, Italy
Proteomics Clin Appl 5:343-53. 2011..Clinical parameters and renin-angiotensin-aldosterone system (RAAS) components were also investigated, on the basis of the well-known relation linking sex female hormones and renin and aldosterone levels...
A 'desaturase hypothesis' for atherosclerosis: Janus-faced enzymes in omega-6 and omega-3 polyunsaturated fatty acid metabolismNicola Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Policlinico G B Rossi, Piazzale L A Scuro 10, Verona, Italy
J Nutrigenet Nutrigenomics 2:129-39. 2009..For these reasons, carriers of specific FADS haplotypes may be predisposed to more pronounced vascular inflammatory damage, but also to an increased beneficial effect with omega-3 PUFA supplementation...
Erythrocyte aging in neurodegenerative disordersL de Franceschi
Department of Clinical and Experimental Medicine, Section of Internal Medicine, University of Verona, Policlinico GB Rossi, P le L Scuro 10, 37134 Verona, Italy
Cell Mol Biol (Noisy-le-grand) 50:179-85. 2004..We have reviewed the mechanism(s) of the loss of red cell membrane stability and of the precocious red cell aging in neurodegenerative disorders...
Genetic polymorphisms of the renin-angiotensin system and atheromatous renal artery stenosisO Olivieri
Department of Clinical and Experimental Medicine, Chair of Internal Medicine, University of Verona, Verona, Italy
Hypertension 34:1097-100. 1999..34, 95% CI 0.19 to 1.47). No significant association was found for AGT M235T and ATR A1166C. Our results suggest a predisposing role for ACE genetic polymorphism in the development and progression of atheromatous RAS...
Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery diseaseO Olivieri
Department of Clinical and Experimental Medicine, Chair of Internal Medicine, University of Verona, Italy
J Hypertens 19:879-84. 2001..The primary object of the paper is to verify this possible association by a rigorous, angiographically controlled study in a large sample of patients with or without multi-vessel CAD...
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery diseaseD Girelli
Department of Clinical and Experimental Medicine, University of Verona, Italy
N Engl J Med 343:774-80. 2000..Since polymorphisms in the factor VII gene contribute to variations in factor VII levels, such polymorphisms may be associated with the risk of myocardial infarction, which is precipitated by thrombosis...
Access rate to the emergency department for venous thromboembolism in relationship with coarse and fine particulate matter air pollutionNicola Martinelli
Section of Internal Medicine, Department of Medicine, University of Verona, Verona, Italy
PLoS ONE 7:e34831. 2012..247; P = 0.012). Our results suggest that short-time exposure to high concentrations of PM(10-2.5) may favour an increased rate of ED accesses for VTE through the induction of a prothrombotic state...
Infective endocarditis with lung and systemic embolization in an injection drug userNicola Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Policlinico G.B. Rossi, 37134 Verona, Italy
Eur Heart J 27:2938. 2006
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolismS Friso
Department of Clinical and Experimental Medicine, University of Verona, Italy
Clin Exp Med 2:7-12. 2002....
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population studyNicola Martinelli
Department of Medicine, University of Verona, Verona, Italy
PLoS ONE 7:e48250. 2012..Due to recently discovered pleiotropic effects of hepcidin, this may worsen insulin resistance and contribute to the cardiovascular complications of MetS...
Deoxygenation affects tyrosine phosphoproteome of red cell membrane from patients with sickle cell diseaseAngela Siciliano
Dept of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Blood Cells Mol Dis 44:233-42. 2010....
Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathyAngela Siciliano
Dept of Medicine, Section of Internal Medicine, University of Verona, Verona, Italy
Haematologica 96:24-32. 2011..Hepatic dysfunction and liver damage may be present in sickle cell disease, but the pathogenesis of these conditions is only partially understood...
Interaction between smoking and PON2 Ser311Cys polymorphism as a determinant of the risk of myocardial infarctionN Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Verona, Italy
Eur J Clin Invest 34:14-20. 2004..We evaluated three PON polymorphisms (PON1 Leu55Met and Gln192Arg; PON2 Ser311Cys) as possible risk factors for coronary atherosclerotic disease (CAD) and/or its main thrombotic complication, myocardial infarction (MI)...
Homocysteine, traditional risk factors and impaired renal function in coronary artery diseaseF Pizzolo
Department of Clinical and Experimental Medicine, University of Verona School of Medicine, Verona, Italy
Eur J Clin Invest 36:698-704. 2006....
Interaction between metabolic syndrome and PON1 polymorphisms as a determinant of the risk of coronary artery diseaseN Martinelli
Department of Clinical and Experimental Medicine, University of Verona, Policlinico G B Rossi, 37134 Verona, Italy
Clin Exp Med 5:20-30. 2005..No increased risk was found for subjects with MS and the 55Met/Met-192Gln/Gln genotype. This study highlights a potential example of genetic (paraoxonase polymorphisms)-clinical (MS) interaction influencing cardiovascular risk...
Recovery of renal function after 3 months of dialysis in a patient with atherosclerotic renovascular disease following aortoiliac bypass and left renal artery reimplantationS Simeoni
Department of Clinical and Experimental Medicine, Chair of Internal Medicine, University of Verona, Verona, Italy
Eur J Vasc Endovasc Surg 28:562-4. 2004
Membrane fatty acids, glutathione-peroxidase activity, and cation transport systems of erythrocytes and malondialdehyde production by platelets in Laurence Moon Barter Biedl syndromeR Corrocher
Istituto di Patologia Medica, , Italy
J Endocrinol Invest 12:475-81. 1989....
Oxidative damage and erythrocyte membrane transport abnormalities in thalassemiasO Olivieri
Department of Internal Medicine, University of Verona, Italy
Blood 84:315-20. 1994..Thus, oxidative damage represents an important factor in the increased activity of the K-Cl cotransport observed in thalassemias, and of the K+ loss observed in beta-thalassemia erythrocytes...
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian populationGong Qing Shen
Department of Molecular Cardiology, Center for Cardiovascular Genetics, Department of Cardiovascular Medicine, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH 44195, USA
J Hum Genet 53:144-50. 2008..These results indicate that chromosome 9p21 confers risk for development of MI in an Italian population...
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate statusSimonetta Friso
Vitamin Metabolism Laboratory, Jean Mayer U S Department of Agriculture Human Nutrition Research on Aging at Tufts University, 711 Washington Street, Boston, MA 02111, USA
Proc Natl Acad Sci U S A 99:5606-11. 2002..03) that is known to be solely represented in those individuals. These results indicate that the MTHFR C677T polymorphism influences DNA methylation status through an interaction with folate status...
Plasma aldosterone assays: comparison between chemiluminescence-based and RIA methodsFrancesca Pizzolo
Clin Chem 52:1431-2. 2006
An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarctionGong Qing Shen
Department of Molecular Cardiology, Lerner Research Institute, Center for Cardiovascular Genetics, Cleveland, OH 44195, USA
Am J Hum Genet 81:780-91. 2007..This extensive study, involving multiple independent populations, provides the first evidence that genetic variants in LRP8 may contribute to the development of premature and familial CAD and MI...
Clinical heterogeneity of acquired hemophilia A: a description of 4 casesMassimo Franchini
Servizio di Immunoematologia e Trasfusione, Azienda Ospedaliera di Verona
Haematologica 90:ECR16. 2005....
Interaction of antibodies against cytomegalovirus with heat-shock protein 60 in pathogenesis of atherosclerosisCaterina Bason
Department of Experimental Medicine, University of Genova, Genova, Italy
Lancet 362:1971-7. 2003....
