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Journal Abstract Search

186 related items for PubMed ID: 17574520

  • 1.
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  • 2. A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
    Yenicesu GI, Cetin M, Ozdemir O, Cetin A, Ozen F, Yenicesu C, Yildiz C, Kocak N.
    Am J Reprod Immunol; 2010 Feb; 63(2):126-36. PubMed ID: 19906129
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  • 3. The role of classic risk factors and prothrombotic factor gene mutations in ischemic stroke risk development in young and middle-aged individuals.
    Supanc V, Sonicki Z, Vukasovic I, Solter VV, Zavoreo I, Kes VB.
    J Stroke Cerebrovasc Dis; 2014 Mar; 23(3):e171-6. PubMed ID: 24189452
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  • 6. Cerebral venous and sinus thrombosis and thrombophilic mutations in Western Iran: association with factor V Leiden.
    Rahimi Z, Mozafari H, Bigvand AH, Doulabi RM, Vaisi-Raygani A, Afshari D, Razazian N, Rezaei M.
    Clin Appl Thromb Hemost; 2010 Aug; 16(4):430-4. PubMed ID: 19703820
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  • 7. Factor V Leiden, prothrombin 20210G --> A, methylenetetrahydrofolate reductase 677C --> T and plasminogen activator inhibitor 4G/5G polymorphism in women with pregnancy-related venous thromboembolism.
    Meglic L, Stegnar M, Milanez T, Bozic M, Peterlin B, Peternel P, Novak-Antolic Z.
    Eur J Obstet Gynecol Reprod Biol; 2003 Dec 10; 111(2):157-63. PubMed ID: 14597244
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  • 9. Plasminogen activator inhibitor-1, factor V, factor II and methylenetetrahydrofolate reductase polymorphisms in women with recurrent miscarriage.
    Pietropolli A, Giuliani E, Bruno V, Patrizi L, Piccione E, Ticconi C.
    J Obstet Gynaecol; 2014 Apr 10; 34(3):229-34. PubMed ID: 24484533
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  • 10. [Progress in relationship between heritable hypercoagulable state and avascular necrosis of femoral head].
    Yin W, Sheng J.
    Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2012 Jun 10; 26(6):695-8. PubMed ID: 22792766
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  • 11. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS, Rihani G.
    Clin Lab Sci; 2004 Jun 10; 17(4):200-2. PubMed ID: 15559724
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  • 13. Role of polymorphisms in factor V (FV Leiden), prothrombin, plasminogen activator inhibitor type-1 (PAI-1), methylenetetrahydrofolate reductase (MTHFR) and cystathionine β-synthase (CBS) genes as risk factors for thrombophilias.
    Miranda-Vilela AL.
    Mini Rev Med Chem; 2012 Sep 01; 12(10):997-1006. PubMed ID: 22512572
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  • 14. [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].
    Kovacheva K, Ivanov P, Konova E, Simeonova M, Komsa-Penkova R.
    Akush Ginekol (Sofiia); 2007 Sep 01; 46(7):10-6. PubMed ID: 18333414
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  • 15. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.
    Almawi WY, Tamim H, Kreidy R, Timson G, Rahal E, Nabulsi M, Finan RR, Irani-Hakime N.
    J Thromb Thrombolysis; 2005 Jun 01; 19(3):189-96. PubMed ID: 16082606
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  • 16. Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared with other populations.
    Settin AA, Alghasham A, Ali A, Dowaidar M, Ismail H.
    Hematology; 2012 May 01; 17(3):176-82. PubMed ID: 22664118
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  • 18. Multiple thrombophilic single nucleotide polymorphisms lack a significant effect on outcomes in fresh IVF cycles: an analysis of 1717 patients.
    Patounakis G, Bergh E, Forman EJ, Tao X, Lonczak A, Franasiak JM, Treff N, Scott RT.
    J Assist Reprod Genet; 2016 Jan 01; 33(1):67-73. PubMed ID: 26545911
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  • 20. Hereditary Thrombophilia and thrombotic events in pregnancy: single-center experience.
    Coriu L, Ungureanu R, Talmaci R, Uscatescu V, Cirstoiu M, Coriu D, Copaciu E.
    J Med Life; 2014 Jan 01; 7(4):567-71. PubMed ID: 25713624
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