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Journal Abstract Search

227 related items for PubMed ID: 9669991

  • 1. Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant.
    Margaglione M, Brancaccio V, Giuliani N, D'Andrea G, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Di Minno G.
    Ann Intern Med; 1998 Jul 15; 129(2):89-93. PubMed ID: 9669991
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  • 2. The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.
    Margaglione M, D'Andrea G, d'Addedda M, Giuliani N, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Brancaccio V, Di Minno G.
    Thromb Haemost; 1998 May 15; 79(5):907-11. PubMed ID: 9609218
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  • 3. The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation.
    De Stefano V, Martinelli I, Mannucci PM, Paciaroni K, Chiusolo P, Casorelli I, Rossi E, Leone G.
    N Engl J Med; 1999 Sep 09; 341(11):801-6. PubMed ID: 10477778
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  • 7. Inherited thrombophilic risk factors and venous thromboembolism: distinct role in peripheral deep venous thrombosis and pulmonary embolism.
    Margaglione M, Brancaccio V, De Lucia D, Martinelli I, Ciampa A, Grandone E, Di Minno G.
    Chest; 2000 Nov 09; 118(5):1405-11. PubMed ID: 11083693
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  • 8. High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives.
    Martinelli I, Sacchi E, Landi G, Taioli E, Duca F, Mannucci PM.
    N Engl J Med; 1998 Jun 18; 338(25):1793-7. PubMed ID: 9632445
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  • 9. Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism.
    Margaglione M, D'Andrea G, Colaizzo D, Cappucci G, del Popolo A, Brancaccio V, Ciampa A, Grandone E, Di Minno G.
    Thromb Haemost; 1999 Dec 18; 82(6):1583-7. PubMed ID: 10613638
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  • 10. Factor V Leiden, prothrombin gene mutation, and thrombosis risk in patients with antiphospholipid antibodies.
    Chopra N, Koren S, Greer WL, Fortin PR, Rauch J, Fortin I, Senécal JL, Docherty P, Hanly JG.
    J Rheumatol; 2002 Aug 18; 29(8):1683-8. PubMed ID: 12180730
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  • 11. Risk of recurrent venous thrombosis in homozygous carriers and double heterozygous carriers of factor V Leiden and prothrombin G20210A.
    Lijfering WM, Middeldorp S, Veeger NJ, Hamulyák K, Prins MH, Büller HR, van der Meer J.
    Circulation; 2010 Apr 20; 121(15):1706-12. PubMed ID: 20368522
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  • 12. Prevalence of factor V Leiden and prothrombin 20210 A variant in Bulgarian patients with pulmonary thromboembolism and deep venous thrombosis.
    Boyanovsky B, Russeva M, Ganev V, Penev M, Baleva M.
    Blood Coagul Fibrinolysis; 2001 Dec 20; 12(8):639-42. PubMed ID: 11734663
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  • 13. 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 20; 81(4):506-10. PubMed ID: 10235429
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  • 14. The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.
    Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, Ardissino D, Palareti G, Bernardi F.
    Arterioscler Thromb Vasc Biol; 1997 Nov 20; 17(11):2418-22. PubMed ID: 9409210
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  • 15. Study of the prothrombin gene 20201 GA variant in FV:Q506 carriers in relationship to the presence or absence of juvenile venous thromboembolism.
    Ehrenforth S, von Depka Prondsinski M, Aygören-Pürsün E, Nowak-Göttl U, Scharrer I, Ganser A.
    Arterioscler Thromb Vasc Biol; 1999 Feb 20; 19(2):276-80. PubMed ID: 9974407
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  • 16. Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia.
    Makris M, Preston FE, Beauchamp NJ, Cooper PC, Daly ME, Hampton KK, Bayliss P, Peake IR, Miller GJ.
    Thromb Haemost; 1997 Dec 20; 78(6):1426-9. PubMed ID: 9423788
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  • 17. Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings.
    Colaizzo D, Amitrano L, Iannaccone L, Vergura P, Cappucci F, Grandone E, Guardascione MA, Margaglione M.
    J Med Genet; 2007 Jun 20; 44(6):412-6. PubMed ID: 17307838
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  • 18. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.
    Gerhardt A, Scharf RE, Beckmann MW, Struve S, Bender HG, Pillny M, Sandmann W, Zotz RB.
    N Engl J Med; 2000 Feb 10; 342(6):374-80. PubMed ID: 10666427
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  • 19. The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis.
    Hillarp A, Zöller B, Svensson PJ, Dahlbäck B.
    Thromb Haemost; 1997 Sep 10; 78(3):990-2. PubMed ID: 9308741
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  • 20. 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 10; 17(1):23-8. PubMed ID: 16607075
    [Abstract] [Full Text] [Related]

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