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Items: 1 to 20 of 124

1.

Sequence variations within the genes related to hemostatic imbalance and their impact on coronary artery disease in Turkish population.

Taymaz H, Erarslan S, Oner ET, Alkan T, Ağirbaşli M, Kirdar B.

Thromb Res. 2007;119(1):55-62. Epub 2006 Feb 10.

PMID:
16472842
2.

Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.

Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.

Blood Coagul Fibrinolysis. 2009 Jun;20(4):252-6. doi: 10.1097/MBC.0b013e3283255487.

PMID:
19349859
3.

Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.

Dölek B, Eraslan S, Eroğlu S, Kesim BE, Ulutin T, Yalçiner A, Laleli YR, Gözükirmizi N.

Clin Appl Thromb Hemost. 2007 Oct;13(4):435-8.

PMID:
17911197
4.

Genetic risk factors in myocardial infarction at young age.

Incalcaterra E, Hoffmann E, Averna MR, Caimi G.

Minerva Cardioangiol. 2004 Aug;52(4):287-312. Review.

PMID:
15284679
5.

The factor V G1691A, factor V H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease.

Ciftdoğan DY, Coşkun S, Ulman C, Tikiz H.

Coron Artery Dis. 2009 Nov;20(7):435-9. doi: 10.1097/MCA.0b013e32832bdb8c.

PMID:
19609209
6.
8.

Association between factor V Leiden mutation and coronary artery disease in the northeast region of Turkey.

Gurlertop HY, Gundogdu F, Pirim I, Islamoglu Y, Egerci N, Sevimli S, Erdem F, Senocak H.

Blood Coagul Fibrinolysis. 2007 Dec;18(8):719-22.

PMID:
17982311
9.

Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.

Yasa MH, Bolaman Z, Yukselen V, Kadikoylu G, Karaoglul AO, Batun S.

Hepatogastroenterology. 2007 Jul-Aug;54(77):1438-42.

PMID:
17708272
10.
11.

Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).

Freitas AI, Mendonça I, Guerra G, Brión M, Reis RP, Carracedo A, Brehm A.

Thromb Res. 2008;122(5):648-56. doi: 10.1016/j.thromres.2008.02.005. Epub 2008 Apr 1.

PMID:
18384842
13.

Absence of factor V Leiden (G1691A) mutation, FII G20210A allele in coronary artery disease in North India.

Gupta N, Khan F, Tripathi M, Singh VP, Tewari S, Ramesh V, Sinha N, Agrawal S.

Indian J Med Sci. 2003 Dec;57(12):535-42.

PMID:
14701945
14.

Human paraoxonase gene polymorphisms and coronary artery disease risk.

Mendonça MI, Dos Reis RP, Freitas AI, Sousa AC, Pereira A, Faria P, Gomes S, Silva B, Santos N, Serrão M, Ornelas I, Freitas S, Araújo JJ, Brehm A, Cardoso AA.

Rev Port Cardiol. 2008 Dec;27(12):1539-55. English, Portuguese.

PMID:
19280995
15.

The -323Ins10 polymorphism for factor VII is not associated with coronary atherosclerosis in symptomatic men. The REGRESS study group.

Lievers KJ, Mennen LI, Rattink AP, Zwinderman AH, Jukema JW, Schouten EG, de Maat MP.

Thromb Res. 2000 Mar 1;97(5):275-80.

PMID:
10709902
17.

Gene-gene interaction affects coronary artery disease risk.

Mendonça MI, Dos Reis RP, Freitas AI, Sousa AC, Pereira A, Faria P, Gomes S, Silva B, Santos N, Serrao M, Ornelas I, Freitas S, Freitas C, Araújo JJ, Brehm A, Cardoso AA.

Rev Port Cardiol. 2009 Apr;28(4):397-415. English, Portuguese.

PMID:
19634497
18.

Prothrombotic gene polymorphisms and atherothrombotic cerebral infarction.

Petrovic D, Milanez T, Kobal J, Bregar D, Potisk KP, Peterlin B.

Acta Neurol Scand. 2003 Aug;108(2):109-13.

PMID:
12859287
19.

Association of the R485K polymorphism of the factor V gene with poor response to activated protein C and increased risk of coronary artery disease in the Chinese population.

Le W, Yu JD, Lu L, Tao R, You B, Cai X, Cao WJ, Huang W, He RM, Zhu DL, Chen Z, Gong LS.

Clin Genet. 2000 Apr;57(4):296-303.

PMID:
10845571
20.

[C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].

Avdonin PV, Kirienko AI, Kozhevnikova LM, Shostak NA, Babadaeva NM, Leont'ev SG, Petukhov EB, Kubatiev AA, Savel'ev VS.

Ter Arkh. 2006;78(6):70-6. Russian.

PMID:
16881367

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