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Journal Abstract Search

248 related items for PubMed ID: 12122980

  • 1.
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  • 2. Evaluation of the interactions of common genetic mutations in stroke subtypes.
    Szolnoki Z, Somogyvári F, Kondacs A, Szabó M, Fodor L.
    J Neurol; 2002 Oct; 249(10):1391-7. PubMed ID: 12382154
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  • 3. [Risk of thrombophilia in carriers of thrombophilic genetic factors in unsuccessful assisted reproduction].
    Ivanov P, Komsa-Penkova R, Kovacheva K, Konova E, Todorova K, Simeonova M, Ivanov I, Stoĭkov S, Popov I, Tanchev S, Bozhinova S.
    Akush Ginekol (Sofiia); 2007 Oct; 46(6):3-8. PubMed ID: 17974163
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  • 4. Connection between genetically determined blood coagulation factors and haemorheology.
    Pongrácz E, Andrikovics H, Bernát IS, Nagy Z.
    Clin Hemorheol Microcirc; 2008 Oct; 39(1-4):333-41. PubMed ID: 18503143
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  • 5. [Platelet glycoprotein IIb/IIIa (LeuPro 33) polymorphism in stroke patients].
    Pongrácz E, Tordai A, Csornai M, Nagy Z.
    Orv Hetil; 2001 Apr 15; 142(15):781-5. PubMed ID: 11367863
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  • 7. Prevalence of thrombophilic mutations and ACE I/D polymorphism in Turkish ischemic stroke patients.
    Celiker G, Can U, Verdi H, Yazici AC, Ozbek N, Atac FB.
    Clin Appl Thromb Hemost; 2009 Apr 15; 15(4):415-20. PubMed ID: 18387982
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  • 10. Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.
    Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I.
    J Rheumatol; 2000 Dec 15; 27(12):2849-54. PubMed ID: 11128675
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  • 13. PLA2 polymorphism of platelet glycoprotein IIb/IIIa but not Factor V Leiden and prothrombin G20210A polymorphisms is associated with venous thromboembolism and more recurrent events in central Iran.
    Pourgheysari B, Boroujeni HR, Hasheminia AM, Drees F.
    Blood Coagul Fibrinolysis; 2013 Jul 15; 24(5):471-6. PubMed ID: 23358226
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  • 14. Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.
    Xenophontos SL, Hadjivassiliou M, Ayrton N, Karagrigoriou A, Pantzaris M, Nicolaides AN, Cariolou MA.
    Int Angiol; 2002 Dec 15; 21(4):322-9. PubMed ID: 12518110
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  • 15. Thrombophilic gene polymorphisms in puerperal cerebral veno-sinus thrombosis.
    Dindagur N, Kruthika-Vinod TP, Christopher R.
    J Neurol Sci; 2006 Nov 01; 249(1):25-30. PubMed ID: 16839569
    [Abstract] [Full Text] [Related]

  • 16. The platelet glycoprotein Ia/IIa gene polymorphism C807T/G873A: a novel risk factor for retinal vein occlusion.
    Dodson PM, Haynes J, Starczynski J, Farmer J, Shigdar S, Fegan G, Johnson RJ, Fegan C.
    Eye (Lond); 2003 Aug 01; 17(6):772-7. PubMed ID: 12928694
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  • 17. [Polymorphisms of ACE-1 and MTHFR genes and genetic susceptibility of ischemic stroke].
    Li C, Zhang C, Qiu S, Lu X, Zeng Y, Wu H, Chen W, Luo W, Liu J.
    Zhonghua Yi Xue Za Zhi; 2002 Aug 10; 82(15):1046-9. PubMed ID: 12194796
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  • 19. Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.
    Kim RJ, Becker RC.
    Am Heart J; 2003 Dec 10; 146(6):948-57. PubMed ID: 14660985
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  • 20. The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis.
    Eroglu A, Egin Y, Cam R, Akar N.
    Ann Hematol; 2009 Jan 10; 88(1):73-6. PubMed ID: 18682947
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