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Journal Abstract Search

267 related items for PubMed ID: 15224376

  • 21. Thrombophilic Mutations Among Patients with Sickle Cell Disease.
    Nefissi RB, Ouali F, Massaoud T, Gritli N.
    Clin Lab; 2017 Nov 01; 63(11):1815-1818. PubMed ID: 29226645
    [Abstract] [Full Text] [Related]

  • 22. 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 01; 88(1):73-6. PubMed ID: 18682947
    [Abstract] [Full Text] [Related]

  • 23. [Mutation frequencies of the thrombophilic state genes in Uzbekistan].
    Sadikova ShE, Karimov KhIa, Muminov ShM, Tulakov RP, Boboev KT.
    Tsitol Genet; 2008 Jan 01; 42(6):50-4. PubMed ID: 19253755
    [Abstract] [Full Text] [Related]

  • 24. Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia.
    Belhaj Nefissi R, Doggui R, Ouali F, Messaoud T, Gritli N.
    Hemoglobin; 2018 Mar 01; 42(2):96-102. PubMed ID: 30200836
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Mutations in clotting factors and inflammatory bowel disease.
    Bernstein CN, Sargent M, Vos HL, Rosendaal FR.
    Am J Gastroenterol; 2007 Feb 01; 102(2):338-43. PubMed ID: 17156138
    [Abstract] [Full Text] [Related]

  • 27. Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.
    Finan RR, Tamim H, Ameen G, Sharida HE, Rashid M, Almawi WY.
    Am J Hematol; 2002 Dec 01; 71(4):300-5. PubMed ID: 12447960
    [Abstract] [Full Text] [Related]

  • 28. Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease.
    Almawi WY, Ameen G, Tamim H, Finan RR, Irani-Hakime N.
    J Thromb Thrombolysis; 2004 Jun 01; 17(3):199-205. PubMed ID: 15353918
    [Abstract] [Full Text] [Related]

  • 29. Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.
    Ozyurek E, Balta G, Degerliyurt A, Parlak H, Aysun S, Gürgey A.
    Clin Appl Thromb Hemost; 2007 Apr 01; 13(2):154-60. PubMed ID: 17456624
    [Abstract] [Full Text] [Related]

  • 30. The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease.
    Moreira Neto F, Lourenço DM, Noguti MA, Morelli VM, Gil IC, Beltrão AC, Figueiredo MS.
    Braz J Med Biol Res; 2006 Oct 01; 39(10):1291-5. PubMed ID: 16906320
    [Abstract] [Full Text] [Related]

  • 31. 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 01; 117(3):547-51. PubMed ID: 17334320
    [Abstract] [Full Text] [Related]

  • 32. Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population.
    Torres JD, Cardona H, Alvarez L, Cardona-Maya W, Castañeda SA, Quintero-Rivera F, Cadavid A, Bedoya G, Tobón L.
    Am J Hematol; 2006 Dec 01; 81(12):933-7. PubMed ID: 16917913
    [Abstract] [Full Text] [Related]

  • 33. [Mutations of genes associated with thromboses in ischemic stroke in patients with primary antiphospholipid syndrome].
    Kalashnikova LA, Dobrynina LA, Patrusheva NL, Kovalenko TF, Patrushev LI, Aleksandrova EN, Berkovskiĭ AL, Sergeeva EV, Nasonov EL.
    Ter Arkh; 2005 Dec 01; 77(10):49-53. PubMed ID: 16320685
    [Abstract] [Full Text] [Related]

  • 34. The prevalence of methylenetetrahydrofolate reductase 677 C-T, factor V 1691 G-A, and prothrombin 20210 G-A mutations in healthy populations in Setif, Algeria.
    Bourouba R, Houcher B, Djabi F, Egin Y, Akar N.
    Clin Appl Thromb Hemost; 2009 Oct 01; 15(5):529-34. PubMed ID: 18840629
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. [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 01; 46(6):3-8. PubMed ID: 17974163
    [Abstract] [Full Text] [Related]

  • 37.
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  • 38. Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.
    Rahimi Z, Vaisi-Raygani A, Nagel RL, Muniz A.
    J Thromb Thrombolysis; 2008 Jun 01; 25(3):288-92. PubMed ID: 17619828
    [Abstract] [Full Text] [Related]

  • 39. Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.
    Lenicek Krleza J, Jakovljevic G, Bronic A, Coen Herak D, Bonevski A, Stepan-Giljevic J, Roic G.
    Pathophysiol Haemost Thromb; 2010 Jun 01; 37(1):24-9. PubMed ID: 20664190
    [Abstract] [Full Text] [Related]

  • 40. 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 01; 19(9):1326-7. PubMed ID: 22721898
    [Abstract] [Full Text] [Related]

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