Turri O - Search Results

1

Serum fetuin-A levels link inflammation and cardiovascular calcification in hemodialysis patients.

Cozzolino M, Galassi A, Biondi ML, Turri O, Papagni S, Mongelli N, Civita L, Gallieni M, Brancaccio D. Cozzolino M, et al. Among authors: turri o. Am J Nephrol. 2006;26(5):423-9. doi: 10.1159/000095782. Epub 2006 Sep 12. Am J Nephrol. 2006. PMID: 16968979

2

Matrix GLA protein gene polymorphisms: clinical correlates and cardiovascular mortality in chronic kidney disease patients.

Brancaccio D, Biondi ML, Gallieni M, Turri O, Galassi A, Cecchini F, Russo D, Andreucci V, Cozzolino M. Brancaccio D, et al. Among authors: turri o. Am J Nephrol. 2005 Nov-Dec;25(6):548-52. doi: 10.1159/000088809. Epub 2005 Oct 5. Am J Nephrol. 2005. PMID: 16210837

3

Matrix metalloproteinase-1 and matrix metalloproteinase-3 gene promoter polymorphisms are associated with mortality in haemodialysis patients.

Cozzolino M, Biondi ML, Galassi A, Turri O, Brancaccio D, Gallieni M. Cozzolino M, et al. Among authors: turri o. Nephrol Dial Transplant. 2009 Jul;24(7):2207-12. doi: 10.1093/ndt/gfp061. Epub 2009 Feb 16. Nephrol Dial Transplant. 2009. PMID: 19221176

4

Matrix metalloproteinase-1 and matrix metalloproteinase-3 gene promoter polymorphisms are associated with carotid artery stenosis.

Ghilardi G, Biondi ML, DeMonti M, Turri O, Guagnellini E, Scorza R. Ghilardi G, et al. Among authors: turri o. Stroke. 2002 Oct;33(10):2408-12. doi: 10.1161/01.str.0000031929.05665.da. Stroke. 2002. PMID: 12364729

5

Ser128Arg gene polymorphism for E-selectin and severity of atherosclerotic arterial disease.

Ghilardi G, Biondi ML, Turri O, Guagnellini E, Scorza R. Ghilardi G, et al. Among authors: turri o. J Cardiovasc Surg (Torino). 2004 Apr;45(2):143-7. J Cardiovasc Surg (Torino). 2004. PMID: 15179350

6

Internal carotid artery occlusive disease and polymorphisms of fractalkine receptor CX3CR1: a genetic risk factor.

Ghilardi G, Biondi ML, Turri O, Guagnellini E, Scorza R. Ghilardi G, et al. Among authors: turri o. Stroke. 2004 Jun;35(6):1276-9. doi: 10.1161/01.STR.0000128528.56009.d4. Epub 2004 Apr 29. Stroke. 2004. PMID: 15118174

7

Independent risk factor for moderate to severe internal carotid artery stenosis: T786C mutation of the endothelial nitric oxide synthase gene.

Ghilardi G, Biondi ML, DeMonti M, Bernini M, Turri O, Massaro F, Guagnellini E, Scorza R. Ghilardi G, et al. Among authors: turri o. Clin Chem. 2002 Jul;48(7):989-93. Clin Chem. 2002. PMID: 12089165

8

Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population.

Biondi ML, Turri O, Dilillo D, Stival G, Guagnellini E. Biondi ML, et al. Among authors: turri o. Clin Chem. 1999 Jun;45(6 Pt 1):897-8. Clin Chem. 1999. PMID: 10352000 No abstract available.

9

SDF1-3'A gene polymorphism is associated with chronic myeloproliferative disease and thrombotic events.

Gerli G, Vanelli C, Turri O, Erario M, Gardellini A, Pugliano M, Biondi ML. Gerli G, et al. Among authors: turri o. Clin Chem. 2005 Dec;51(12):2411-4. doi: 10.1373/clinchem.2005.057802. Clin Chem. 2005. PMID: 16306115 No abstract available.

10

High resolution melting analysis to genotype the most common variants in the HFE gene.

Marotta RV, Turri O, Morandi A, Murano M, d'Eril GM, Biondi ML. Marotta RV, et al. Among authors: turri o. Clin Chem Lab Med. 2011 Sep;49(9):1453-7. doi: 10.1515/CCLM.2011.237. Epub 2011 Jun 1. Clin Chem Lab Med. 2011. PMID: 21627541

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