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Journal Abstract Search

212 related items for PubMed ID: 12506156

  • 1. Outcome of kidney transplantation in patients with inherited thrombophilia: data of a prospective study.
    Heidenreich S, Junker R, Wolters H, Lang D, Hessing S, Nitsche G, Nowak-Göttl U.
    J Am Soc Nephrol; 2003 Jan; 14(1):234-9. PubMed ID: 12506156
    [Abstract] [Full Text] [Related]

  • 2. Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.
    Kader HA, Berman WF, Al-Seraihy AS, Ware RE, Ulshen MH, Treem WR.
    J Pediatr Gastroenterol Nutr; 2002 Nov; 35(5):629-35. PubMed ID: 12454577
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.
    Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Ramírez-Cisneros FJ.
    Am J Hematol; 2001 Jan 01; 66(1):28-31. PubMed ID: 11426488
    [Abstract] [Full Text] [Related]

  • 6. Role of genetic prothrombotic risk factors in childhood caval vein thrombosis.
    Münchow N, Kosch A, Schobess R, Junker R, Auberger K, Nowak-Göttl U.
    Eur J Pediatr; 1999 Dec 01; 158 Suppl 3():S109-12. PubMed ID: 10650847
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Prothrombotic risk factors in children with spontaneous venous thrombosis and their asymptomatic parents: a family study.
    Kosch A, Junker R, Kurnik K, Schobess R, Günther G, Koch H, Nowak-Göttl U.
    Thromb Res; 2000 Sep 15; 99(6):531-7. PubMed ID: 10974337
    [Abstract] [Full Text] [Related]

  • 9. Prevalence of three prothrombotic polymorphisms. Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina. On behalf of the Grupo Cooperativo Argentino de Hemostasia y Trombosis.
    Genoud V, Castañon M, Annichino-Bizzacchi J, Korin J, Kordich L.
    Thromb Res; 2000 Nov 01; 100(3):127-31. PubMed ID: 11108898
    [No Abstract] [Full Text] [Related]

  • 10. Abdominal venous thrombosis in neonates and infants: role of prothrombotic risk factors - a multicentre case-control study. For the Childhood Thrombophilia Study Group.
    Heller C, Schobess R, Kurnik K, Junker R, Günther G, Kreuz W, Nowak-Göttl U.
    Br J Haematol; 2000 Nov 01; 111(2):534-9. PubMed ID: 11122096
    [Abstract] [Full Text] [Related]

  • 11. Inherited thrombophilia genes in minorities.
    Mack R, Chowdary D, Streck D, Dermody J.
    Genet Test; 1999 Nov 01; 3(4):371-3. PubMed ID: 10627946
    [Abstract] [Full Text] [Related]

  • 12. 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]

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  • 14. High rate of acute rejections in renal allograft recipients with thrombophilic risk factors.
    Heidenreich S, Dercken C, August C, Koch HG, Nowak-Göttl U.
    J Am Soc Nephrol; 1998 Jul 10; 9(7):1309-13. PubMed ID: 9644643
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Inherited prothrombotic risk factors in Turkish children with acute lymphoblastic leukemia: significance of concomitant genetic mutation.
    Torun YA, Patiroglu T, Ozdemir MA, Ozkul Y, Ekici A, Karakukcu M.
    Clin Appl Thromb Hemost; 2012 Jan 01; 18(2):218-21. PubMed ID: 21873357
    [Abstract] [Full Text] [Related]

  • 17. Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.
    Cadoni G, Scipione S, Rocca B, Agostino S, La Greca C, Bonvissuto D, Paludetti G.
    Ann Otol Rhinol Laryngol; 2006 Mar 01; 115(3):195-200. PubMed ID: 16572609
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 27; 42(2):96-102. PubMed ID: 30200836
    [Abstract] [Full Text] [Related]

  • 20. Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population.
    Angelopoulou K, Nicolaides A, Constantinou Deltas C.
    Clin Appl Thromb Hemost; 2000 Apr 27; 6(2):104-7. PubMed ID: 10775032
    [Abstract] [Full Text] [Related]

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