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Journal Abstract Search

397 related items for PubMed ID: 17974163

  • 1. [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; 46(6):3-8. PubMed ID: 17974163
    [Abstract] [Full Text] [Related]

  • 2. [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; 46(7):10-6. PubMed ID: 18333414
    [Abstract] [Full Text] [Related]

  • 3. [High risk of recurrent spontaneous abortion during second trimester in women carriers of polymorphism A2 in platelet glycoprotein IIb/IIIa].
    Ivanov P, Komsa-Penkova R, Ivanov I, Konova E, Kovacheva K, Stoĭkov S, Popov I.
    Akush Ginekol (Sofiia); 2008; 47(4):3-9. PubMed ID: 19230252
    [Abstract] [Full Text] [Related]

  • 4. Embryo implantation after assisted reproductive procedures and maternal thrombophilia.
    Martinelli I, Taioli E, Ragni G, Levi-Setti P, Passamonti SM, Battaglioli T, Lodigiani C, Mannucci PM.
    Haematologica; 2003 Jul; 88(7):789-93. PubMed ID: 12857558
    [Abstract] [Full Text] [Related]

  • 5. 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; 21(10):2694-8. PubMed ID: 16835215
    [Abstract] [Full Text] [Related]

  • 6. [Inherited thrombophilic factors in women with secondary infertility].
    Ivanov P, Gecheva S, Tsvyatkovska T, Georgieva G, Komsa-Penkova R, Konova E, Simeonova M, Tanchev S.
    Akush Ginekol (Sofiia); 2012 Oct; 51(4):3-7. PubMed ID: 23234018
    [Abstract] [Full Text] [Related]

  • 7. 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; 24(5):471-6. PubMed ID: 23358226
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. [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]

  • 10. Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke.
    Glueck CJ, Fontaine RN, Wang P.
    Thromb Haemost; 2001 Feb 20; 85(2):256-9. PubMed ID: 11246543
    [Abstract] [Full Text] [Related]

  • 11. Impact of thrombophilic genetic factors on pulmonary embolism: early onset and recurrent incidences.
    Ivanov P, Komsa-Penkova R, Kovacheva K, Ivanov Y, Stoyanova A, Ivanov I, Pavlov P, Glogovska P, Nojarov V.
    Lung; 2008 Feb 20; 186(1):27-36. PubMed ID: 18097719
    [Abstract] [Full Text] [Related]

  • 12. Repeated in vitro fertilization failure and its relation with thrombophilia.
    Simur A, Ozdemir S, Acar H, Colakoğlu MC, Görkemli H, Balci O, Nergis S.
    Gynecol Obstet Invest; 2009 Feb 20; 67(2):109-12. PubMed ID: 18957855
    [Abstract] [Full Text] [Related]

  • 13. 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 Feb 20; 54(77):1438-42. PubMed ID: 17708272
    [Abstract] [Full Text] [Related]

  • 14. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS, Rihani G.
    Clin Lab Sci; 2004 Feb 20; 17(4):200-2. PubMed ID: 15559724
    [Abstract] [Full Text] [Related]

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  • 17. 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 20; 16(4):430-4. PubMed ID: 19703820
    [Abstract] [Full Text] [Related]

  • 18. Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening.
    Fábregues F, Tàssies D, Reverter JC, Carmona F, Ordinas A, Balasch J.
    Fertil Steril; 2004 Apr 20; 81(4):989-95. PubMed ID: 15066453
    [Abstract] [Full Text] [Related]

  • 19. 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 20; 30(7):921-5. PubMed ID: 19618008
    [Abstract] [Full Text] [Related]

  • 20. 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 20; 82(1):6-9. PubMed ID: 10456445
    [Abstract] [Full Text] [Related]

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