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Journal Abstract Search

706 related items for PubMed ID: 18682947

  • 21. Role of thrombotic risk factors in end-stage renal disease.
    Tripathi G, Sankhwar SN, Sharma RK, Baburaj VP, Agrawal S.
    Clin Appl Thromb Hemost; 2010 Apr; 16(2):132-40. PubMed ID: 19520684
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. Impact of thrombophilic gene mutations on thrombosis risk in patients with gastrointestinal carcinoma.
    Pihusch R, Danzl G, Scholz M, Harich D, Pihusch M, Lohse P, Hiller E.
    Cancer; 2002 Jun 15; 94(12):3120-6. PubMed ID: 12115343
    [Abstract] [Full Text] [Related]

  • 24. 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 15; 19(3):189-96. PubMed ID: 16082606
    [Abstract] [Full Text] [Related]

  • 25. [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 Jun 15; 46(7):10-6. PubMed ID: 18333414
    [Abstract] [Full Text] [Related]

  • 26. No association of factor V Leiden, prothrombin G20210A, and MTHFR C677T gene polymorphisms with kidney allograft survival: a multicenter study.
    Meyer M, Laux G, Scherer S, Tran TH, Opelz G, Mytilineos J.
    Transplantation; 2007 Apr 27; 83(8):1055-8. PubMed ID: 17452895
    [Abstract] [Full Text] [Related]

  • 27. 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 27; 30(7):921-5. PubMed ID: 19618008
    [Abstract] [Full Text] [Related]

  • 28. Dihydrofolate reductase (DHRF) 19-bp intron-1 deletion and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms in breast cancer.
    Cam R, Eroglu A, Egin Y, Akar N.
    Breast Cancer Res Treat; 2009 May 27; 115(2):431-2. PubMed ID: 18498051
    [No Abstract] [Full Text] [Related]

  • 29. 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 27; 16(4):430-4. PubMed ID: 19703820
    [Abstract] [Full Text] [Related]

  • 30. Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes.
    Alhenc-Gelas M, Arnaud E, Nicaud V, Aubry ML, Fiessinger JN, Aiach M, Emmerich J.
    Thromb Haemost; 1999 Apr 27; 81(4):506-10. PubMed ID: 10235429
    [Abstract] [Full Text] [Related]

  • 31. Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.
    Ben Salem-Berrabah O, Fekih-Mrissa N, N'siri B, Ben Hamida A, Benammar-Elgaaied A, Gritli N, Mrissa R.
    J Clin Neurosci; 2012 Sep 27; 19(9):1326-7. PubMed ID: 22721898
    [Abstract] [Full Text] [Related]

  • 32. Genetic and acquired prothrombotic risk factors and sudden hearing loss.
    Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, Censuales S, Pignataro L.
    Laryngoscope; 2007 Mar 27; 117(3):547-51. PubMed ID: 17334320
    [Abstract] [Full Text] [Related]

  • 33. MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
    Cruciani F, Moramarco A, Curto T, Labate A, Recupero V, Conti L, Gandolfo GM, Balacco Gabrieli C.
    Clin Ter; 2003 Mar 27; 154(5):299-303. PubMed ID: 14994919
    [Abstract] [Full Text] [Related]

  • 34. Factor V Leiden, prothrombin G20210A and MTHFR gene mutations in inflammatory bowel disease.
    Törüner M, Erkan O, Soykan I, Bozdayi M, Cetinkaya H, Yurdaydin C, Uzunalimoğlu O, Ozden A.
    Turk J Gastroenterol; 2004 Dec 27; 15(4):250-2. PubMed ID: 16249980
    [Abstract] [Full Text] [Related]

  • 35. [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 Dec 27; 46(6):3-8. PubMed ID: 17974163
    [Abstract] [Full Text] [Related]

  • 36. ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: a study of 180 homozygotes for the Factor V Leiden mutation.
    Procare-GEHT Group.
    Br J Haematol; 2006 Dec 27; 135(5):697-702. PubMed ID: 17107352
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection.
    Jara-Prado A, Alonso ME, Martínez Ruano L, Guerrero Camacho J, Leyva A, López M, Gutierrez-Castrellon P, Arauz A.
    Int J Stroke; 2010 Apr 01; 5(2):80-5. PubMed ID: 20446941
    [Abstract] [Full Text] [Related]

  • 39. Prevalence of factor V G1691A (Leiden) and prothrombin G20210A polymorphisms among apparently healthy Jordanians.
    Nusier MK, Radaideh AM, Ababneh NA, Qaqish BM, Alzoubi R, Khader Y, Mersa JY, Irshaid NM, El-Khateeb M.
    Neuro Endocrinol Lett; 2007 Oct 01; 28(5):699-703. PubMed ID: 17984931
    [Abstract] [Full Text] [Related]

  • 40. Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia.
    Fawaz NA, Bashawery L, Al-Sheikh I, Qatari A, Al-Othman SS, Almawi WY.
    Am J Hematol; 2004 Jul 01; 76(3):307-9. PubMed ID: 15224376
    [Abstract] [Full Text] [Related]

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