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234 related items for PubMed ID: 16283309

  • 1. Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis.
    Koshy A, Jeyakumari M.
    Ann Hematol; 2006 Feb; 85(2):126-8. PubMed ID: 16283309
    [Abstract] [Full Text] [Related]

  • 2. Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India.
    Bhattacharyya M, Makharia G, Kannan M, Ahmed RP, Gupta PK, Saxena R.
    Am J Clin Pathol; 2004 Jun; 121(6):844-7. PubMed ID: 15198356
    [Abstract] [Full Text] [Related]

  • 3. Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis.
    Amitrano L, Brancaccio V, Guardascione MA, Margaglione M, Iannaccone L, D'Andrea G, Marmo R, Ames PR, Balzano A.
    Hepatology; 2000 Feb; 31(2):345-8. PubMed ID: 10655256
    [Abstract] [Full Text] [Related]

  • 4. High FVIII level is associated with idiopathic portal vein thrombosis in South India.
    Koshy A, Jeyakumari M.
    Am J Med; 2007 Jun; 120(6):552.e9-11. PubMed ID: 17524760
    [Abstract] [Full Text] [Related]

  • 5. The prothrombin gene G20210A variant and puerperal cerebral venous and sinus thrombosis in South Indian women.
    Nagaraja D, Kruthika-Vinod TP, Christopher R.
    J Clin Neurosci; 2007 Jul; 14(7):635-8. PubMed ID: 17433691
    [Abstract] [Full Text] [Related]

  • 6. Factor V Leiden and prothrombin gene G20210A mutations are uncommon in portal vein thrombosis in India.
    Sharma S, Kumar SI, Poddar U, Yachha SK, Aggarwal R.
    Indian J Gastroenterol; 2006 Jul; 25(5):236-9. PubMed ID: 17090840
    [Abstract] [Full Text] [Related]

  • 7. Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis.
    Amitrano L, Guardascione MA, Brancaccio V, Margaglione M, Manguso F, Iannaccone L, Grandone E, Balzano A.
    J Hepatol; 2004 May; 40(5):736-41. PubMed ID: 15094219
    [Abstract] [Full Text] [Related]

  • 8. Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population.
    Torres JD, Cardona H, Alvarez L, Cardona-Maya W, Castañeda SA, Quintero-Rivera F, Cadavid A, Bedoya G, Tobón L.
    Am J Hematol; 2006 Dec; 81(12):933-7. PubMed ID: 16917913
    [Abstract] [Full Text] [Related]

  • 9. Inherited thrombophilic abnormalities and risk of portal vein thrombosis. a meta-analysis.
    Dentali F, Galli M, Gianni M, Ageno W.
    Thromb Haemost; 2008 Apr; 99(4):675-82. PubMed ID: 18392325
    [Abstract] [Full Text] [Related]

  • 10. [Portal vein thrombosis associated with a myeloproliferative disorder, prothrombin G20210A mutation, antiphospholipid syndrome, with repermeation during anticoagulant therapy].
    Diaz E, Nahon S, Charachon A, Traissac L, Lenoble M, Challier E, Delas N.
    Gastroenterol Clin Biol; 2001 May; 25(5):549-51. PubMed ID: 11521110
    [Abstract] [Full Text] [Related]

  • 11. Interrelation of hyperhomocysteinemia and inherited risk factors for venous thromboembolism. Results from the E.D.I.TH. study: a hospital-based case-control study.
    Oger E, Lacut K, Le Gal G, Couturaud F, Abalain JH, Mercier B, Mottier D, EDITH (Etude des Déterminants/Interaction de la THrombose veineuse) Collaborative Study Group.
    Thromb Res; 2007 May; 120(2):207-14. PubMed ID: 17126889
    [Abstract] [Full Text] [Related]

  • 12. Prothrombin G20210A mutation in Turkish children with thrombosis and the frequency of prothrombin C20209T.
    Gurgey A, Unal S, Okur H, Duru F, Gumruk F.
    Pediatr Hematol Oncol; 2005 Jun; 22(4):309-14. PubMed ID: 16020118
    [Abstract] [Full Text] [Related]

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  • 14. Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients.
    Altinisik J, Ates O, Ulutin T, Cengiz M, Buyru N.
    Clin Appl Thromb Hemost; 2008 Oct; 14(4):415-20. PubMed ID: 18160601
    [Abstract] [Full Text] [Related]

  • 15. Frequent factor II G20210A mutation in idiopathic portal vein thrombosis.
    Chamouard P, Pencreach E, Maloisel F, Grunebaum L, Ardizzone JF, Meyer A, Gaub MP, Goetz J, Baumann R, Uring-Lambert B, Levy S, Dufour P, Hauptmann G, Oudet P.
    Gastroenterology; 1999 Jan; 116(1):144-8. PubMed ID: 9869612
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  • 17. 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]

  • 18. Hereditary thrombophilia as a cause of Budd-Chiari syndrome: a study from Western India.
    Mohanty D, Shetty S, Ghosh K, Pawar A, Abraham P.
    Hepatology; 2001 Oct; 34(4 Pt 1):666-70. PubMed ID: 11584361
    [Abstract] [Full Text] [Related]

  • 19. Associations of coagulation factor V Leiden and prothrombin G20210A mutations with Budd-Chiari syndrome and portal vein thrombosis: a systematic review and meta-analysis.
    Qi X, Ren W, De Stefano V, Fan D.
    Clin Gastroenterol Hepatol; 2014 Nov; 12(11):1801-12.e7. PubMed ID: 24793031
    [Abstract] [Full Text] [Related]

  • 20. [Cerebral venous thrombosis and familial prothrombin gene G20210a mutation].
    Verdelho A, Ferro JM, Palmeiro A, Antunes C.
    Rev Neurol; 2014 Nov; 33(4):335-8. PubMed ID: 11588727
    [Abstract] [Full Text] [Related]

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