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69 related items for PubMed ID: 19776610

  • 1. Relationship between preterm labor and thrombophilic gene polymorphism: A prospective sequential cohort study.
    Uvuz F, Kilic S, Yilmaz N, Tuncay G, Cakar E, Yuksel B, Bilge U.
    Gynecol Obstet Invest; 2009; 68(4):234-8. PubMed ID: 19776610
    [Abstract] [Full Text] [Related]

  • 2. Thrombophilic polymorphisms in preterm delivery.
    Valdez LL, Quintero A, Garcia E, Olivares N, Celis A, Rivas F, Rivas F.
    Blood Cells Mol Dis; 2004; 33(1):51-6. PubMed ID: 15223011
    [Abstract] [Full Text] [Related]

  • 3. Relationship between polymorphisms in thrombophilic genes and preeclampsia in a Brazilian population.
    Dalmáz CA, Santos KG, Botton MR, Tedoldi CL, Roisenberg I.
    Blood Cells Mol Dis; 2006; 37(2):107-10. PubMed ID: 16963292
    [Abstract] [Full Text] [Related]

  • 4. 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. PubMed ID: 19349859
    [Abstract] [Full Text] [Related]

  • 5. The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population.
    Said JM, Brennecke SP, Moses EK, Walker SP, Monagle PT, Campbell J, Bryant VJ, Borg AJ, Higgins JR.
    Aust N Z J Obstet Gynaecol; 2008 Dec; 48(6):536-41. PubMed ID: 19133039
    [Abstract] [Full Text] [Related]

  • 6. [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 Dec; 46(7):10-6. PubMed ID: 18333414
    [Abstract] [Full Text] [Related]

  • 7. [Genetics of blood coagulation in young stroke patients].
    Pongrácz E, Tordai A, Csornai M, Nagy Z.
    Ideggyogy Sz; 2002 Mar 20; 55(3-4):111-7. PubMed ID: 12122980
    [Abstract] [Full Text] [Related]

  • 8. Atypical timing and presentation of periventricular haemorrhagic infarction in preterm infants: the role of thrombophilia.
    Harteman JC, Groenendaal F, van Haastert IC, Liem KD, Stroink H, Bierings MB, Huisman A, de Vries LS.
    Dev Med Child Neurol; 2012 Feb 20; 54(2):140-7. PubMed ID: 22098125
    [Abstract] [Full Text] [Related]

  • 9. [Relationship between three thrombophilic gene mutations and unexplained recurrent early spontaneous abortion].
    Xu L, Liu XM, Zhang HY, Zhao J, Qi QW, Chang YF.
    Zhonghua Fu Chan Ke Za Zhi; 2007 Mar 20; 42(3):180-3. PubMed ID: 17537304
    [Abstract] [Full Text] [Related]

  • 10. 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 Mar 20; 15(4):415-20. PubMed ID: 18387982
    [Abstract] [Full Text] [Related]

  • 11. [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 Mar 20; 46(6):3-8. PubMed ID: 17974163
    [Abstract] [Full Text] [Related]

  • 12. Thrombophilic polymorphisms--factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations--and preterm birth.
    Resch B, Gallistl S, Kutschera J, Mannhalter C, Muntean W, Mueller WD.
    Wien Klin Wochenschr; 2004 Sep 30; 116(17-18):622-6. PubMed ID: 15515881
    [Abstract] [Full Text] [Related]

  • 13. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause.
    Brenner B, Sarig G, Weiner Z, Younis J, Blumenfeld Z, Lanir N.
    Thromb Haemost; 1999 Jul 30; 82(1):6-9. PubMed ID: 10456445
    [Abstract] [Full Text] [Related]

  • 14. 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 30; 88(1):73-6. PubMed ID: 18682947
    [Abstract] [Full Text] [Related]

  • 15. Thrombophilia-related genetic variations in patients with pulmonary embolism in the main teaching hospital in Jordan.
    Obeidat NM, Awidi A, Sulaiman NA, Abu-Khader IB.
    Saudi Med J; 2009 Jul 30; 30(7):921-5. PubMed ID: 19618008
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty.
    Philipp CS, Dilley A, Saidi P, Evatt B, Austin H, Zawadsky J, Harwood D, Ellingsen D, Barnhart E, Phillips DJ, Hooper WC.
    Thromb Haemost; 1998 Dec 01; 80(6):869-73. PubMed ID: 9869151
    [Abstract] [Full Text] [Related]

  • 18. Genetic thrombophilic mutations among couples with recurrent miscarriage.
    Jivraj S, Rai R, Underwood J, Regan L.
    Hum Reprod; 2006 May 01; 21(5):1161-5. PubMed ID: 16431900
    [Abstract] [Full Text] [Related]

  • 19. Analysis of prothrombotic mutations and polymorphisms in children who developed thrombosis in the perioperative period of congenital cardiac surgery.
    Ozbek N, Ataç FB, Yildirim SV, Verdi H, Yazici C, Yilmaz BT, Tokel NK.
    Cardiol Young; 2005 Feb 01; 15(1):19-25. PubMed ID: 15831156
    [Abstract] [Full Text] [Related]

  • 20. Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failure.
    Qublan HS, Eid SS, Ababneh HA, Amarin ZO, Smadi AZ, Al-Khafaji FF, Khader YS.
    Hum Reprod; 2006 Oct 01; 21(10):2694-8. PubMed ID: 16835215
    [Abstract] [Full Text] [Related]

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