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PUBMED FOR HANDHELDS

Journal Abstract Search


206 related items for PubMed ID: 15716659

  • 1.
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  • 2. 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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  • 3. Causes of portal venous thrombosis in cirrhotic patients: the role of genetic and acquired factors.
    Mangia A, Villani MR, Cappucci G, Santoro R, Ricciardi R, Facciorusso D, Leandro G, Caruso N, Andriulli A.
    Eur J Gastroenterol Hepatol; 2005 Jul; 17(7):745-51. PubMed ID: 15947552
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  • 4. Portal vein thrombosis in children and adolescents: the low prevalence of hereditary thrombophilic disorders.
    Pinto RB, Silveira TR, Bandinelli E, Röhsig L.
    J Pediatr Surg; 2004 Sep; 39(9):1356-61. PubMed ID: 15359390
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  • 5. Thrombophilic factor analysis in cirrhotic patients with portal vein thrombosis.
    Saugel B, Lee M, Feichtinger S, Hapfelmeier A, Schmid RM, Siveke JT.
    J Thromb Thrombolysis; 2015 Jul; 40(1):54-60. PubMed ID: 25115839
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  • 8. 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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  • 10. 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; 19(3):189-96. PubMed ID: 16082606
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  • 12. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
    Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.
    Blood Coagul Fibrinolysis; 2009 Jun; 20(4):252-6. PubMed ID: 19349859
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  • 13. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
    Yasa MH, Bolaman Z, Yukselen V, Kadikoylu G, Karaoglul AO, Batun S.
    Hepatogastroenterology; 2007 Jun; 54(77):1438-42. PubMed ID: 17708272
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  • 14. Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study.
    El-Karaksy H, El-Koofy N, El-Hawary M, Mostafa A, Aziz M, El-Shabrawi M, Mohsen NA, Kotb M, El-Raziky M, El-Sonoon MA, A-Kader H.
    Ann Hematol; 2004 Nov; 83(11):712-5. PubMed ID: 15309526
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  • 15. MTHFR C677TT, PAI1 4G-4G, V Leiden Q506, and prothrombin G20210A in hepatocellular carcinoma with and without portal vein thrombosis.
    D'Amico M, Pasta L, Sammarco P.
    J Thromb Thrombolysis; 2009 Jul; 28(1):70-3. PubMed ID: 18618228
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  • 17. Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study.
    Koylu MT, Kucukevcilioglu M, Erdurman FC, Durukan AH, Sobacı G, Torun D, Tunca Y, Ayyildiz O.
    Ophthalmic Genet; 2017 Jul; 38(4):352-356. PubMed ID: 28085519
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