These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

400 related items for PubMed ID: 15198356

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study.
    Janssen HL, Meinardi JR, Vleggaar FP, van Uum SH, Haagsma EB, van Der Meer FJ, van Hattum J, Chamuleau RA, Adang RP, Vandenbroucke JP, van Hoek B, Rosendaal FR.
    Blood; 2000 Oct 01; 96(7):2364-8. PubMed ID: 11001884
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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 01; 17(1):23-8. PubMed ID: 16607075
    [Abstract] [Full Text] [Related]

  • 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 01; 96(5):1448-54. PubMed ID: 11374681
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 12(11):1801-12.e7. PubMed ID: 24793031
    [Abstract] [Full Text] [Related]

  • 10. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
    Kabukcu S, Keskin N, Keskin A, Atalay E.
    Clin Appl Thromb Hemost; 2007 Apr 01; 13(2):166-71. PubMed ID: 17456626
    [Abstract] [Full Text] [Related]

  • 11. Thrombophilia in young patients with acute myocardial infarction.
    Celik M, Altintas A, Celik Y, Karabulut A, Ayyildiz O.
    Saudi Med J; 2008 Jan 01; 29(1):48-54. PubMed ID: 18176672
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 81(12):933-7. PubMed ID: 16917913
    [Abstract] [Full Text] [Related]

  • 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 Dec 01; 54(77):1438-42. PubMed ID: 17708272
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Prevalence of prothrombotic factors in patients with Budd-Chiari syndrome or non-cirrhotic nonmalignant portal vein thrombosis: A hospital-based observational study.
    Fan J, Wang Q, Luo B, Chen H, Wang Z, Niu J, Yuan J, Yuan X, Bai W, He C, Guo W, Li K, Yin Z, Fan D, Han G.
    J Gastroenterol Hepatol; 2020 Jul 01; 35(7):1215-1222. PubMed ID: 31711259
    [Abstract] [Full Text] [Related]

  • 16. MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
    Cruciani F, Moramarco A, Curto T, Labate A, Recupero V, Conti L, Gandolfo GM, Balacco Gabrieli C.
    Clin Ter; 2003 Jul 01; 154(5):299-303. PubMed ID: 14994919
    [Abstract] [Full Text] [Related]

  • 17. Maternal cerebral venous thrombosis, uncommon but serious disorder, pathologic predictors and contribution of prothrombotic abnormalities.
    Klai S, Fekih-Mrissa N, Mrissa R, Rachdi R, Gritli N.
    Blood Coagul Fibrinolysis; 2013 Apr 01; 24(3):269-72. PubMed ID: 23337711
    [Abstract] [Full Text] [Related]

  • 18. [Mutation frequencies of the thrombophilic state genes in Uzbekistan].
    Sadikova ShE, Karimov KhIa, Muminov ShM, Tulakov RP, Boboev KT.
    Tsitol Genet; 2008 Apr 01; 42(6):50-4. PubMed ID: 19253755
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 14(4):415-20. PubMed ID: 18160601
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 85(2):126-8. PubMed ID: 16283309
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.