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Results: 1 to 20 of 91

Similar articles for PubMed (Select 23537071)

1.

Association between UCP2 A55V polymorphism and risk of cardiovascular events in patients with multi-vessel coronary arterial disease.

Gioli-Pereira L, Santos PC, Sugaya LS, Ferreira NE, Krieger JE, Pereira AC, Hueb WA.

BMC Med Genet. 2013 Mar 27;14:40. doi: 10.1186/1471-2350-14-40.

2.

Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21.

Gioli-Pereira L, Santos PC, Ferreira NE, Hueb WA, Krieger JE, Pereira AC.

BMC Cardiovasc Disord. 2012 Aug 2;12:61. doi: 10.1186/1471-2261-12-61.

3.

Dynamic regulation of MTHFR mRNA expression and C677T genotype modulate mortality in coronary artery disease patients after revascularization.

Pereira AC, Miyakawa AA, Lopes NH, Soares PR, de Oliveira SA, Cesar LA, Ramires JF, Hueb W, Krieger JE.

Thromb Res. 2007;121(1):25-32. Epub 2007 Jul 2.

PMID:
17604826
4.

Association between ADAMTS13 polymorphisms and risk of cardiovascular events in chronic coronary disease.

Schettert IT, Pereira AC, Lopes NH, Hueb WA, Krieger JE.

Thromb Res. 2010 Jan;125(1):61-6. doi: 10.1016/j.thromres.2009.03.008. Epub 2009 May 8.

PMID:
19427680
5.

Effect of glycoprotein IIIa PlA2 polymorphism on outcome of patients with stable coronary artery disease and effect of smoking.

Lopes NH, Pereira AC, Hueb W, Soares PR, Lanz JR, Gersh BJ, de Oliveira S, Cesar LA, Ramires JF, Krieger JE.

Am J Cardiol. 2004 Jun 15;93(12):1469-72.

PMID:
15194015
6.

The common G-866A polymorphism of the UCP2 gene and survival in diabetic patients following myocardial infarction.

Palmer BR, Devereaux CL, Dhamrait SS, Mocatta TJ, Pilbrow AP, Frampton CM, Skelton L, Yandle TG, Winterbourn CC, Richards AM, Montgomery HE, Cameron VA.

Cardiovasc Diabetol. 2009 Jun 15;8:31. doi: 10.1186/1475-2840-8-31.

7.

Association between platelet P2Y12 haplotype and risk of cardiovascular events in chronic coronary disease.

Schettert IT, Pereira AC, Lopes NH, Hueb WA, Krieger JE.

Thromb Res. 2006;118(6):679-83. Epub 2006 Jan 6.

PMID:
16405973
8.

The common -866G>A variant in the promoter of UCP2 is associated with decreased risk of coronary artery disease in type 2 diabetic men.

Cheurfa N, Dubois-Laforgue D, Ferrarezi DA, Reis AF, Brenner GM, Bouché C, Le Feuvre C, Fumeron F, Timsit J, Marre M, Velho G.

Diabetes. 2008 Apr;57(4):1063-8. doi: 10.2337/db07-1292. Epub 2008 Jan 11.

9.

Influence of 677 C-->T polymorphism of methylenetetrahydrofolate reductase on medium-term prognosis after acute coronary syndromes.

García-Pinilla JM, Espinosa-Caliani S, Jiménez-Navarro M, Gómez-Doblas JJ, Cabrera-Bueno F, Reyes-Engel A, de Teresa-Galván E.

Tex Heart Inst J. 2007;34(2):142-7.

10.

C677T polymorphism of the methylenetetrahydrofolate reductase gene is a risk factor of adverse events after coronary revascularization.

Botto N, Andreassi MG, Rizza A, Berti S, Bevilacqua S, Federici C, Palmieri C, Glauber M, Biagini A.

Int J Cardiol. 2004 Sep;96(3):341-5.

PMID:
15301885
11.

UCP2 A55V variant is associated with obesity and related phenotypes in an aboriginal community in Taiwan.

Wang TN, Huang MC, Lin HL, Hsiang CH, Ko AM, Chang WT, Ko YC.

Int J Obes (Lond). 2007 Nov;31(11):1746-52. Epub 2007 May 15.

PMID:
17502873
12.

TCF7L2 polymorphism rs7903146 is associated with coronary artery disease severity and mortality.

Sousa AG, Marquezine GF, Lemos PA, Martinez E, Lopes N, Hueb WA, Krieger JE, Pereira AC.

PLoS One. 2009 Nov 17;4(11):e7697. doi: 10.1371/journal.pone.0007697.

13.

Clinical judgment and treatment options in stable multivessel coronary artery disease: results from the one-year follow-up of the MASS II (Medicine, Angioplasty, or Surgery Study II).

Pereira AC, Lopes NH, Soares PR, Krieger JE, de Oliveira SA, Cesar LA, Ramires JA, Hueb W.

J Am Coll Cardiol. 2006 Sep 5;48(5):948-53. Epub 2006 Aug 17.

14.

Plasma leptin levels are related to body composition, sex, insulin levels and the A55V polymorphism of the UCP2 gene.

Rance KA, Johnstone AM, Murison S, Duncan JS, Wood SG, Speakman JR.

Int J Obes (Lond). 2007 Aug;31(8):1311-8. Epub 2007 Mar 6.

PMID:
17342078
15.

Impact of number of vessels disease on outcome of patients with stable coronary artery disease: 5-year follow-up of the Medical, Angioplasty, and bypass Surgery study (MASS).

Lopes NH, Paulitsch Fda S, Gois AF, Pereira AC, Stolf NA, Dallan LO, Ramires JA, Hueb WA.

Eur J Cardiothorac Surg. 2008 Mar;33(3):349-54. doi: 10.1016/j.ejcts.2007.11.025. Epub 2008 Jan 30.

PMID:
18249128
16.

Endovascular treatment of lower extremity arteries is associated with an improved outcome in diabetic patients affected by intermittent claudication.

Giugliano G, Perrino C, Schiano V, Brevetti L, Sannino A, Schiattarella GG, Gargiulo G, Serino F, Ferrone M, Scudiero F, Carbone A, Bruno A, Amato B, Trimarco B, Esposito G.

BMC Surg. 2012;12 Suppl 1:S19. doi: 10.1186/1471-2482-12-S1-S19. Epub 2012 Nov 15.

17.

The GPIIIA PlA2 polymorphism is associated with an increased risk of cardiovascular adverse events.

Galasso G, Santulli G, Piscione F, De Rosa R, Trimarco V, Piccolo R, Cassese S, Iaccarino G, Trimarco B, Chiariello M.

BMC Cardiovasc Disord. 2010 Sep 16;10:41. doi: 10.1186/1471-2261-10-41.

18.

[The association between A55V variant in UCP2 gene and body fat distribution, serum lipid profile in Chinese].

Zheng Y, Xiang K, Zhang R, Jia W, Lu J, Tang J, Li J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2000 Apr;17(2):97-100. Chinese.

PMID:
10751530
19.

Changes in fat mass after initiation of maintenance dialysis is influenced by the uncoupling protein 2 exon 8 insertion/deletion polymorphism.

Wang X, Axelsson J, Nordfors L, Qureshi AR, Avesani C, Barany P, Schalling M, Heimbürger O, Lindholm B, Stenvinkel P.

Nephrol Dial Transplant. 2007 Jan;22(1):196-202. Epub 2006 Sep 17.

20.

AMPD1 (C34T) polymorphism and clinical outcomes in patients undergoing myocardial revascularization.

Andreassi MG, Botto N, Laghi-Pasini F, Manfredi S, Ghelarducci B, Farneti A, Solinas M, Biagini A, Picano E.

Int J Cardiol. 2005 May 25;101(2):191-5.

PMID:
15882662
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