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Journal Abstract Search

381 related items for PubMed ID: 9822524

  • 1. Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations.
    Grandone E, Margaglione M, Colaizzo D, D'Andrea G, Cappucci G, Brancaccio V, Di Minno G.
    Am J Obstet Gynecol; 1998 Nov; 179(5):1324-8. PubMed ID: 9822524
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Genetic polymorphisms associated with acute pulmonary embolism and deep venous thrombosis.
    Nizankowska-Mogilnicka E, Adamek L, Grzanka P, Domagala TB, Sanak M, Krzanowski M, Szczeklik A.
    Eur Respir J; 2003 Jan 10; 21(1):25-30. PubMed ID: 12570104
    [Abstract] [Full Text] [Related]

  • 4. Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages.
    Foka ZJ, Lambropoulos AF, Saravelos H, Karas GB, Karavida A, Agorastos T, Zournatzi V, Makris PE, Bontis J, Kotsis A.
    Hum Reprod; 2000 Feb 10; 15(2):458-62. PubMed ID: 10655323
    [Abstract] [Full Text] [Related]

  • 5. [Factor V Leiden, FII G20210A, MTHFR C677T mutations as risk factors for venous thrombosis during pregnancy and puerperium].
    Dordević V, Rakićević L, Spasić M, Miković D, Kovać M, Radojković D.
    Vojnosanit Pregl; 2005 Mar 10; 62(3):201-5. PubMed ID: 15790048
    [Abstract] [Full Text] [Related]

  • 6. Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease.
    Couturaud F, Oger E, Abalain JH, Chenu E, Guias B, Floch HH, Mercier B, Mottier D, Leroyer C.
    Respiration; 2000 Mar 10; 67(6):657-61. PubMed ID: 11124649
    [Abstract] [Full Text] [Related]

  • 7. 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 10; 19(3):189-96. PubMed ID: 16082606
    [Abstract] [Full Text] [Related]

  • 8. Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population.
    Lu Y, Zhao Y, Liu G, Wang X, Liu Z, Chen B, Hui R.
    Thromb Res; 2002 Apr 01; 106(1):7-12. PubMed ID: 12165282
    [Abstract] [Full Text] [Related]

  • 9. The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels.
    Cattaneo M, Chantarangkul V, Taioli E, Santos JH, Tagliabue L.
    Thromb Res; 1999 Jan 01; 93(1):1-8. PubMed ID: 10065893
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 27(12):2849-54. PubMed ID: 11128675
    [Abstract] [Full Text] [Related]

  • 11. Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment.
    Salomon O, Steinberg DM, Zivelin A, Gitel S, Dardik R, Rosenberg N, Berliner S, Inbal A, Many A, Lubetsky A, Varon D, Martinowitz U, Seligsohn U.
    Arterioscler Thromb Vasc Biol; 1999 Mar 01; 19(3):511-8. PubMed ID: 10073951
    [Abstract] [Full Text] [Related]

  • 12. Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.
    Nowak-Göttl U, Wermes C, Junker R, Koch HG, Schobess R, Fleischhack G, Schwabe D, Ehrenforth S.
    Blood; 1999 Mar 01; 93(5):1595-9. PubMed ID: 10029588
    [Abstract] [Full Text] [Related]

  • 13. Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.
    Mueller T, Marschon R, Dieplinger B, Haidinger D, Gegenhuber A, Poelz W, Webersinke G, Haltmayer M.
    J Vasc Surg; 2005 May 01; 41(5):808-15. PubMed ID: 15886665
    [Abstract] [Full Text] [Related]

  • 14. Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR.
    Hessner MJ, Luhm RA, Pearson SL, Endean DJ, Friedman KD, Montgomery RR.
    Thromb Haemost; 1999 May 01; 81(5):733-8. PubMed ID: 10365746
    [Abstract] [Full Text] [Related]

  • 15. Factor V Leiden and prothrombin 20210 G-A mutations in controls and in patients with thromboembolic events during pregnancy or the puerperium.
    Yilmazer M, Kurtay G, Sonmezer M, Akar N.
    Arch Gynecol Obstet; 2003 Oct 01; 268(4):304-8. PubMed ID: 14504875
    [Abstract] [Full Text] [Related]

  • 16. Factor V Leiden, prothrombin 20210G --> A, methylenetetrahydrofolate reductase 677C --> T and plasminogen activator inhibitor 4G/5G polymorphism in women with pregnancy-related venous thromboembolism.
    Meglic L, Stegnar M, Milanez T, Bozic M, Peterlin B, Peternel P, Novak-Antolic Z.
    Eur J Obstet Gynecol Reprod Biol; 2003 Dec 10; 111(2):157-63. PubMed ID: 14597244
    [Abstract] [Full Text] [Related]

  • 17. [C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].
    Avdonin PV, Kirienko AI, Kozhevnikova LM, Shostak NA, Babadaeva NM, Leont'ev SG, Petukhov EB, Kubatiev AA, Savel'ev VS.
    Ter Arkh; 2006 Dec 10; 78(6):70-6. PubMed ID: 16881367
    [Abstract] [Full Text] [Related]

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  • 20. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors.
    Antoniadi T, Hatzis T, Kroupis C, Economou-Petersen E, Petersen MB.
    Am J Hematol; 1999 Aug 10; 61(4):265-7. PubMed ID: 10440914
    [Abstract] [Full Text] [Related]

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