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Journal Abstract Search

371 related items for PubMed ID: 15831156

  • 1. Analysis of prothrombotic mutations and polymorphisms in children who developed thrombosis in the perioperative period of congenital cardiac surgery.
    Ozbek N, Ataç FB, Yildirim SV, Verdi H, Yazici C, Yilmaz BT, Tokel NK.
    Cardiol Young; 2005 Feb; 15(1):19-25. PubMed ID: 15831156
    [Abstract] [Full Text] [Related]

  • 2. 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; 88(1):73-6. PubMed ID: 18682947
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  • 4. Mutations in clotting factors and inflammatory bowel disease.
    Bernstein CN, Sargent M, Vos HL, Rosendaal FR.
    Am J Gastroenterol; 2007 Feb; 102(2):338-43. PubMed ID: 17156138
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.
    Miñano A, Ordóñez A, España F, González-Porras JR, Lecumberri R, Fontcuberta J, Llamas P, Marín F, Estellés A, Alberca I, Vicente V, Corral J.
    Haematologica; 2008 May; 93(5):729-34. PubMed ID: 18387978
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  • 8. 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; 117(3):547-51. PubMed ID: 17334320
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  • 9. Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay?
    Djordjevic V, Stankovic M, Brankovic-Sreckovic V, Rakicevic L, Radojkovic D.
    J Child Neurol; 2009 Jul; 24(7):823-7. PubMed ID: 19372095
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  • 10. Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis.
    Silingardi M, Salvarani C, Boiardi L, Accardo P, Iorio A, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Ciccia F, Ghirarduzzi A, Filippini D, Paolazzi G, Iori I.
    Arthritis Rheum; 2004 Apr 15; 51(2):177-83. PubMed ID: 15077257
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  • 11. Prothrombotic gene polymorphisms: possible contributors to hepatic artery thrombosis after orthotopic liver transplantation.
    Pereboom IT, Adelmeijer J, van der Steege G, van den Berg AP, Lisman T, Porte RJ.
    Transplantation; 2011 Sep 15; 92(5):587-93. PubMed ID: 21836539
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  • 12. Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.
    Kim RJ, Becker RC.
    Am Heart J; 2003 Dec 15; 146(6):948-57. PubMed ID: 14660985
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  • 14. Potential thrombophilic mutations/polymorphisms in patients with no flow-limiting stenosis after myocardial infarction.
    French JK, Van de Water NS, Sutton TM, Lund M, Gao W, McDowell J, Liu-Stratton Y, Pohorence J, Szymanski D, Goldschmidt-Clermont P, White HD, Browett PJ, Cooke G.
    Am Heart J; 2003 Jan 15; 145(1):118-24. PubMed ID: 12514663
    [Abstract] [Full Text] [Related]

  • 15. Nonstroke arterial thrombosis in children: Hacettepe experience.
    Balci YI, Unal S, Gumruk F, Cetin M, Ozkutlu S, Gurgey A.
    Blood Coagul Fibrinolysis; 2008 Sep 15; 19(6):519-24. PubMed ID: 18685435
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  • 16. ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: a study of 180 homozygotes for the Factor V Leiden mutation.
    Procare-GEHT Group.
    Br J Haematol; 2006 Dec 15; 135(5):697-702. PubMed ID: 17107352
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  • 17. Factor V Leiden and increased risk for arterial thrombotic disease in young Brazilian patients.
    de Paula Sabino A, Ribeiro DD, Carvalho Md, Cardoso J, Dusse LM, Fernandes AP.
    Blood Coagul Fibrinolysis; 2006 Jun 15; 17(4):271-5. PubMed ID: 16651869
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  • 18. The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls.
    Gohil R, Peck G, Sharma P.
    Thromb Haemost; 2009 Aug 15; 102(2):360-70. PubMed ID: 19652888
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  • 19. Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.
    Xenophontos SL, Hadjivassiliou M, Ayrton N, Karagrigoriou A, Pantzaris M, Nicolaides AN, Cariolou MA.
    Int Angiol; 2002 Dec 15; 21(4):322-9. PubMed ID: 12518110
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  • 20. Thrombophilic polymorphisms in preterm delivery.
    Valdez LL, Quintero A, Garcia E, Olivares N, Celis A, Rivas F, Rivas F.
    Blood Cells Mol Dis; 2004 Dec 15; 33(1):51-6. PubMed ID: 15223011
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