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413 related items for PubMed ID: 10655256

  • 1. 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
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  • 2. The platelet glycoprotein Ia/IIa gene polymorphism C807T/G873A: a novel risk factor for retinal vein occlusion.
    Dodson PM, Haynes J, Starczynski J, Farmer J, Shigdar S, Fegan G, Johnson RJ, Fegan C.
    Eye (Lond); 2003 Aug; 17(6):772-7. PubMed ID: 12928694
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  • 3. 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; 27(12):2849-54. PubMed ID: 11128675
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  • 4. 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; 79(5):907-11. PubMed ID: 9609218
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  • 5. 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
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  • 6. 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
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  • 7. Thrombophilic gene mutations in cirrhotic patients with portal vein thrombosis.
    Erkan O, Bozdayi AM, Disibeyaz S, Oguz D, Ozcan M, Bahar K, Karayalcin S, Ozden A, Bozkaya H, Yurdaydin C, Uzunalimoglu O.
    Eur J Gastroenterol Hepatol; 2005 Mar; 17(3):339-43. PubMed ID: 15716659
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  • 8. Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease.
    Guédon C, Le Cam-Duchez V, Lalaude O, Ménard JF, Lerebours E, Borg JY.
    Am J Gastroenterol; 2001 May; 96(5):1448-54. PubMed ID: 11374681
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  • 10. 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
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  • 11. 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
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  • 17. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives.
    Aznar J, Vayá A, Estellés A, Mira Y, Seguí R, Villa P, Ferrando F, Falcó C, Corella D, España F.
    Haematologica; 2000 Dec; 85(12):1271-6. PubMed ID: 11114134
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  • 18. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].
    Guo C, Guo Q, Gong Y, Chen B, Liu Q, Li J, Gao G, Zhou H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):295-7. PubMed ID: 12170465
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  • 19. Genetic risk factors for superficial vein thrombosis.
    Martinelli I, Cattaneo M, Taioli E, De Stefano V, Chiusolo P, Mannucci PM.
    Thromb Haemost; 1999 Oct; 82(4):1215-7. PubMed ID: 10544900
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  • 20. 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
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