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Items: 1 to 20 of 73

1.

Polymorphism of C3 complement in association with myocardial infarction in a sample of central Tunisia.

Leban N, Jraba K, Chalghoum A, Hassine S, Elhayek D, Denden S, Lakhdhar R, Maatoug F, Gamra H, Braham H, Ben Chibani J, Khelil AH.

Diagn Pathol. 2013 Jun 13;8:93. doi: 10.1186/1746-1596-8-93.

2.

Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction.

Császár A, Duba J, Melegh B, Kramer J, Szalai C, Prohászka Z, Karádi I, Kovács M, Méhes K, Romics L, Füst G.

Exp Clin Immunogenet. 2001;18(4):206-12.

PMID:
11872951
3.

Association of genetic markers with coronary heart disease (myocardial infarction)--a case-control study.

Golabi P, Kshatriya GK, Kapoor AK.

J Indian Med Assoc. 1999 Jan;97(1):6-7.

PMID:
10549177
4.

[C3 complement polymorphism in patients suffering from obstructive chronic bronchopneumopathy in Tunisia].

Leban N, Haj Khelil A, Daimi H, Denden S, Slimene F, Mehdouani K, Abdennaji Guenounou B, Lefranc G, Perrin P, Ben Chibani J.

Ann Biol Clin (Paris). 2007 May-Jun;65(3):251-6. French.

5.

Association of a DNA polymorphism of the apolipoprotein AI-CIII-AIV gene cluster with myocardial infarction in a Tunisian population.

Sediri Y, Kallel A, Feki M, Mourali S, Elasmi M, Abdessalem S, Mechmeche R, Jemaa R, Kaabachi N.

Eur J Intern Med. 2011 Aug;22(4):407-11. doi: 10.1016/j.ejim.2011.03.002. Epub 2011 Apr 21.

PMID:
21767760
6.

Chromosome 1p13 genetic variants antagonize the risk of myocardial infarction associated with high ApoB serum levels.

Gigante B, Leander K, Vikström M, Ye S, de Faire U.

BMC Cardiovasc Disord. 2012 Oct 16;12:90. doi: 10.1186/1471-2261-12-90.

7.

Genetic association analysis of myocardial infarction with thrombospondin-1 N700S variant in a Chinese population.

Zhou X, Huang J, Chen J, Zhao J, Ge D, Yang W, Gu D.

Thromb Res. 2004;113(3-4):181-6.

PMID:
15140581
8.

Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction.

Berredjeb Ben Slama D, Fekih-Mrissa N, Haggui A, Nsiri B, Baraket N, Haouala H, Gritli N.

Cardiovasc Pathol. 2013 Jan-Feb;22(1):39-41. doi: 10.1016/j.carpath.2012.03.002. Epub 2012 Apr 5.

PMID:
22483732
9.
10.

Association of angiotensin-converting enzyme gene 2350G>A polymorphism with myocardial infarction in a Chinese population.

Min Pan, Jiang MH, Wei MF, Liu ZH, Jiang WP, Geng HH, Cui ZC, Zhang DL, Zhu JH.

Clin Appl Thromb Hemost. 2009 Jul-Aug;15(4):435-42. doi: 10.1177/1076029608316013. Epub 2008 Apr 28.

PMID:
18445609
11.

Association analysis of the IL-17F His161Arg polymorphism in myocardial infarction.

Pei F, Han Y, Zhang X, Yan C, Huang M, Deng J, Kang J.

Coron Artery Dis. 2009 Dec;20(8):513-7. doi: 10.1097/MCA.0b013e328332a6c3.

PMID:
19838108
12.

A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study.

Kardys I, Klaver CC, Despriet DD, Bergen AA, Uitterlinden AG, Hofman A, Oostra BA, Van Duijn CM, de Jong PT, Witteman JC.

J Am Coll Cardiol. 2006 Apr 18;47(8):1568-75. Epub 2006 Mar 29.

13.

An association study of thrombospondin 1 and 2 SNPs with coronary artery disease and myocardial infarction among South Indians.

Ashokkumar M, Anbarasan C, Saibabu R, Kuram S, Raman SC, Cherian KM.

Thromb Res. 2011 Oct;128(4):e49-53. doi: 10.1016/j.thromres.2011.05.026. Epub 2011 Jul 16.

PMID:
21762961
14.

Polymorphisms in the CC-chemokine receptor-2 (CCR2) and -5 (CCR5) genes and risk of myocardial infarction among Tunisian male patients.

Kallel A, Abdessalem S, Sédiri Y, Mourali MS, Feki M, Mechmeche R, Jemaa R, Kaabachi N.

Clin Biochem. 2012 Apr;45(6):420-4. doi: 10.1016/j.clinbiochem.2012.01.004. Epub 2012 Jan 20.

PMID:
22285384
15.

Polymorphisms of the NOS3 gene and risk of myocardial infarction in the Tunisian population.

Kallel A, Sbaï MH, Sediri Y, Abdessalem S, Mourali MS, Feki M, Mechmeche R, Jemaa R, Kaabachi N.

Cytokine. 2013 Dec;64(3):646-51. doi: 10.1016/j.cyto.2013.09.005. Epub 2013 Oct 3.

PMID:
24095258
16.

Adiponectin gene polymorphisms and their effect on the risk of myocardial infarction and type 2 diabetes: an association study in an Italian population.

Chiodini BD, Specchia C, Gori F, Barlera S, D'Orazio A, Pietri S, Crociati L, Nicolucci A, Franciosi M, Signorini S, Brambilla P, Grazia Franzosi M; GISSI Prevenzione Investigators; SiBioC-GISSI Prevenzione Group.

Ther Adv Cardiovasc Dis. 2010 Aug;4(4):223-30. doi: 10.1177/1753944710371483. Epub 2010 Jun 24.

PMID:
20576642
17.

Inflammatory cytokine gene variants in coronary artery disease patients in Greece.

Manginas A, Tsiavou A, Chaidaroglou A, Giamouzis G, Degiannis D, Panagiotakos D, Cokkinos DV.

Coron Artery Dis. 2008 Dec;19(8):575-82. doi: 10.1097/MCA.0b013e32831286e8.

PMID:
19005292
18.

Association of ANRIL polymorphism (rs1333049:C>G) with myocardial infarction and its pharmacogenomic role in hypercholesterolemia.

Ahmed W, Ali IS, Riaz M, Younas A, Sadeque A, Niazi AK, Niazi SH, Ali SH, Azam M, Qamar R.

Gene. 2013 Feb 25;515(2):416-20. doi: 10.1016/j.gene.2012.12.044. Epub 2012 Dec 21.

PMID:
23266621
19.

[Association of Rs10487667 genetic polymorphism of thromboxane synthase with myocardial infarction in Uigur population of Xinjiang].

Wang BZ, Ma YT, Fu ZY, Xie X, Zhang XL, Chen BD, Liu F, Yu ZX.

Zhonghua Yu Fang Yi Xue Za Zhi. 2010 Nov;44(11):1032-6. Chinese.

PMID:
21215134
20.

Variants in the coagulation factor 2 receptor (F2R) gene influence the risk of myocardial infarction in men through an interaction with interleukin 6 serum levels.

Gigante B, Vikström M, Meuzelaar LS, Chernogubova E, Silveira A, Hooft FV, Hamsten A, de Faire U.

Thromb Haemost. 2009 May;101(5):943-53.

PMID:
19404549

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