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Results: 1 to 20 of 150

Similar articles for PubMed (Select 18037749)

1.

A985G polymorphism of the endothelin-2 gene and atrial fibrillation in patients with hypertrophic cardiomyopathy.

Nagai T, Ogimoto A, Okayama H, Ohtsuka T, Shigematsu Y, Hamada M, Miki T, Higaki J.

Circ J. 2007 Dec;71(12):1932-6.

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Functional polymorphisms in ACE and CYP11B2 genes and atrial fibrillation in patients with hypertensive heart disease.

Huang M, Gai X, Yang X, Hou J, Lan X, Zheng W, Chen F, He J.

Clin Chem Lab Med. 2009;47(1):32-7. doi: 10.1515/CCLM.2009.023.

PMID:
19117407
4.

Association of MMP-9 gene polymorphisms with atrial fibrillation in hypertensive heart disease patients.

Gai X, Lan X, Luo Z, Wang F, Liang Y, Zhang H, Zhang W, Hou J, Huang M.

Clin Chim Acta. 2009 Oct;408(1-2):105-9. doi: 10.1016/j.cca.2009.07.020. Epub 2009 Aug 7.

PMID:
19665460
5.

Hypertrophic cardiomyopathy in the elderly: significance of atrial fibrillation.

Doi Y, Kitaoka H.

J Cardiol. 2001;37 Suppl 1:133-8.

PMID:
11433817
6.

MMP-2 and TIMP-2 gene polymorphisms and susceptibility to atrial fibrillation in Chinese Han patients with hypertensive heart disease.

Gai X, Zhang Z, Liang Y, Chen Z, Yang X, Hou J, Lan X, Zheng W, Hou J, Huang M.

Clin Chim Acta. 2010 May 2;411(9-10):719-24. doi: 10.1016/j.cca.2010.02.002. Epub 2010 Feb 9.

PMID:
20138860
7.

Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation.

Firouzi M, Ramanna H, Kok B, Jongsma HJ, Koeleman BP, Doevendans PA, Groenewegen WA, Hauer RN.

Circ Res. 2004 Aug 20;95(4):e29-33. Epub 2004 Aug 5.

8.

MinK gene polymorphism in the pathogenesis of lone atrial fibrillation.

Prystupa A, Dzida G, Myśliński W, Małaj G, Lorenc T.

Kardiol Pol. 2006 Nov;64(11):1205-11; discussion 1212-3. English, Polish.

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Prognostic value of two polymorphisms in non-sarcomeric genes for the development of atrial fibrillation in patients with hypertrophic cardiomyopathy.

Orenes-Piñero E, Hernández-Romero D, Romero-Aniorte AI, Martínez M, García-Honrubia A, Caballero L, Garrigos-Gómez N, Andreu-Cayuelas JM, González J, Feliu E, Climent V, Nicolás-Ruiz F, De La Morena G, Valdés M, Lip GY, Marín F.

QJM. 2014 Aug;107(8):613-21. doi: 10.1093/qjmed/hcu046. Epub 2014 Mar 5.

11.

The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).

Sinner MF, Pfeufer A, Akyol M, Beckmann BM, Hinterseer M, Wacker A, Perz S, Sauter W, Illig T, Näbauer M, Schmitt C, Wichmann HE, Schömig A, Steinbeck G, Meitinger T, Kääb S.

Eur Heart J. 2008 Apr;29(7):907-14. doi: 10.1093/eurheartj/ehm619. Epub 2008 Jan 25.

12.

The single nucleotide polymorphisms of Kir3.4 gene and their correlation with lone paroxysmal atrial fibrillation in Chinese Han population.

Zhang C, Yuan GH, Cheng ZF, Xu MW, Hou LF, Wei FP.

Heart Lung Circ. 2009 Aug;18(4):257-61. doi: 10.1016/j.hlc.2008.12.002. Epub 2009 Feb 8.

PMID:
19208499
13.

Polymorphisms of angiotensin-converting enzyme 2 gene associated with magnitude of left ventricular hypertrophy in male patients with hypertrophic cardiomyopathy.

Wang SX, Fu CY, Zou YB, Wang H, Shi Y, Xu XQ, Chen JZ, Song XD, Huan TJ, Hui RT.

Chin Med J (Engl). 2008 Jan 5;121(1):27-31.

PMID:
18208662
14.

Lone and secondary nonvalvular atrial fibrillation: role of a genetic susceptibility.

Fatini C, Sticchi E, Gensini F, Gori AM, Marcucci R, Lenti M, Michelucci A, Genuardi M, Abbate R, Gensini GF.

Int J Cardiol. 2007 Aug 9;120(1):59-65. Epub 2006 Nov 20.

PMID:
17113662
15.

Genetic polymorphism of KCNH2 confers predisposition of acquired atrial fibrillation in Chinese.

Wang QS, Wang XF, Chen XD, Yu JF, Wang J, Sun J, Lu SB, Shen MY, Lu M, Li YG, Jin L.

J Cardiovasc Electrophysiol. 2009 Oct;20(10):1158-62. doi: 10.1111/j.1540-8167.2009.01494.x. Epub 2009 May 20.

PMID:
19490382
16.

The association of human connexin 40 genetic polymorphisms with atrial fibrillation.

Juang JM, Chern YR, Tsai CT, Chiang FT, Lin JL, Hwang JJ, Hsu KL, Tseng CD, Tseng YZ, Lai LP.

Int J Cardiol. 2007 Mar 2;116(1):107-12. Epub 2006 Jun 30.

PMID:
16814413
17.

Absence of connexin 40 gene polymorphism, as a marker of undetected atrial fibrillation in patients with unexplained cerebral ischemic events.

Chaldoupi SM, Soedamah-Muthu SS, Regieli J, Werf Cv, Nelen M, van der Smagt JJ, Algra A, Hauer RN, Doevendans PA, Loh P.

Eur J Cardiovasc Prev Rehabil. 2009 Oct;16(5):616-20. doi: 10.1097/HJR.0b013e32832da03a.

PMID:
19494781
18.

P-wave durations as a predictor for atrial fibrillation development in patients with hypertrophic cardiomyopathy.

Ozdemir O, Soylu M, Demir AD, Topaloglu S, Alyan O, Turhan H, Bicer A, Kutuk E.

Int J Cardiol. 2004 Apr;94(2-3):163-6. Erratum in: Int J Cardiol. 2004 Dec;97(3):581.

PMID:
15093974
19.

[Association of rs1805127 polymorphism of KCNE1 gene with atrial fibrillation in Uigur population of Xinjiang].

Yao J, Ma YT, Xie X, Liu F, Chen BD, An Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):436-40. doi: 10.3760/cma.j.issn.1003-9406.2011.04.018. Chinese.

PMID:
21811988
20.

Relationship between -344T/C polymorphism in the aldosterone synthase gene and atrial fibrillation in patients with essential hypertension.

Sun X, Yang J, Hou X, Li J, Shi Y, Jing Y.

J Renin Angiotensin Aldosterone Syst. 2011 Dec;12(4):557-63. doi: 10.1177/1470320311417654. Epub 2011 Aug 16.

PMID:
21846681
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