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Journal Abstract Search

427 related items for PubMed ID: 19366087

  • 1. Recurrent thrombembolic risk in patients with multiple thrombophilic disorders.
    Agoşton-Coldea L, Rusu LD, Bobar C, Rusu ML, Mocan T, Procopciuc LM.
    Rom J Intern Med; 2008; 46(3):261-6. PubMed ID: 19366087
    [Abstract] [Full Text] [Related]

  • 2. Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation.
    González-Porras JR, García-Sanz R, Alberca I, López ML, Balanzategui A, Gutierrez O, Lozano F, San Miguel J.
    Blood Coagul Fibrinolysis; 2006 Jan; 17(1):23-8. PubMed ID: 16607075
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  • 3. Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.
    Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I.
    J Rheumatol; 2000 Dec; 27(12):2849-54. PubMed ID: 11128675
    [Abstract] [Full Text] [Related]

  • 4. [Mutation frequencies of the thrombophilic state genes in Uzbekistan].
    Sadikova ShE, Karimov KhIa, Muminov ShM, Tulakov RP, Boboev KT.
    Tsitol Genet; 2008 Dec; 42(6):50-4. PubMed ID: 19253755
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  • 5. 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 Dec; 54(77):1438-42. PubMed ID: 17708272
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  • 7. 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]

  • 8. 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; 19(9):1326-7. PubMed ID: 22721898
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  • 10. 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 Sep; 37(1):24-9. PubMed ID: 20664190
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  • 12. Thrombophilias and recurrent pregnancy loss.
    Kutteh WH, Triplett DA.
    Semin Reprod Med; 2006 Feb; 24(1):54-66. PubMed ID: 16418978
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  • 13. [Genetic determinants of hereditary thrombophilia in pathogenesis of venous thrombosis].
    Kapustin SI, Blinov MN, Kargin VD, Filanovskaia LI, Saltykova NB, Beliazo OE, Golovina OG, Shmeleva VM, Panshina AM, Papaian LP.
    Ter Arkh; 2003 Feb; 75(10):78-80. PubMed ID: 14669613
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  • 15. Superficial venous thrombosis: prevalence of common genetic risk factors and their role on spreading to deep veins.
    Milio G, Siragusa S, Minà C, Amato C, Corrado E, Grimaudo S, Novo S.
    Thromb Res; 2008 Feb; 123(2):194-9. PubMed ID: 18387654
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  • 17. Combined genetic mutations have remarkable effect on deep venous thrombosis and/or pulmonary embolism occurence.
    Simsek E, Yesilyurt A, Pinarli F, Eyerci N, Ulus AT.
    Gene; 2014 Feb 15; 536(1):171-6. PubMed ID: 24334115
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  • 18. Easy, accurate and reliable screening for SNPs by ion pair/reverse phase HPLC: simultaneous detection of factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T variants.
    Neitzel B, Matern C, Holinski-Feder E.
    Clin Lab; 2003 Feb 15; 49(7-8):313-8. PubMed ID: 12908731
    [Abstract] [Full Text] [Related]

  • 19. Massive pulmonary embolism associated with Factor V Leiden, prothrombin, and methylenetetrahydrofolate reductase gene mutations in a young patient on oral contraceptive pills: a case report.
    Charafeddine KM, Mahfouz RA, Ibrahim GY, Taher AT, Hoballah JJ, Taha AM.
    Clin Appl Thromb Hemost; 2010 Oct 15; 16(5):594-8. PubMed ID: 19520679
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  • 20. [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 Oct 15; 46(7):10-6. PubMed ID: 18333414
    [Abstract] [Full Text] [Related]

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