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322 related items for PubMed ID: 8592550

  • 1. Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosis.
    Mandel H, Brenner B, Berant M, Rosenberg N, Lanir N, Jakobs C, Fowler B, Seligsohn U.
    N Engl J Med; 1996 Mar 21; 334(12):763-8. PubMed ID: 8592550
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  • 2. Activated protein C resistance--a major risk factor for thrombosis.
    Rosén SB, Sturk A.
    Eur J Clin Chem Clin Biochem; 1997 Jul 21; 35(7):501-16. PubMed ID: 9263726
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  • 3. "Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds.
    Simioni P, Scudeller A, Radossi P, Gavasso S, Girolami B, Tormene D, Girolami A.
    Thromb Haemost; 1996 Mar 21; 75(3):422-6. PubMed ID: 8701401
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  • 6. 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 21; 83(11):712-5. PubMed ID: 15309526
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  • 7. Factor V Leiden (Arg506Gln), a confounding genetic risk factor but not mandatory for the occurrence of venous thromboembolism in homozygotes and obligate heterozygotes for cystathionine beta-synthase deficiency.
    Yap S, O'Donnell KA, O'Neill C, Mayne PD, Thornton P, Naughten E.
    Thromb Haemost; 1999 Apr 21; 81(4):502-5. PubMed ID: 10235428
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  • 8. The factor V Leiden mutation which predisposes to thrombosis is not common in patients with antiphospholipid syndrome.
    Dizon-Townson D, Hutchison C, Silver R, Branch DW, Ward K.
    Thromb Haemost; 1995 Oct 21; 74(4):1029-31. PubMed ID: 8560406
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  • 9. Factor V Leiden mutation: an unrecognized cause of hemiplegic cerebral palsy, neonatal stroke, and placental thrombosis.
    Thorarensen O, Ryan S, Hunter J, Younkin DP.
    Ann Neurol; 1997 Sep 21; 42(3):372-5. PubMed ID: 9307261
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  • 13. 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 21; 17(1):23-8. PubMed ID: 16607075
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  • 15. Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency.
    Kalkanoğlu HS, Coşkun T, Aydoğdu SD, Tokatli A, Gürgey A.
    J Inherit Metab Dis; 2001 Jun 21; 24(3):367-9. PubMed ID: 11486902
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  • 16. Selective screening for the Factor V Leiden mutation: is it advisable prior to the prescription of oral contraceptives?
    Schambeck CM, Schwender S, Haubitz I, Geisen UE, Grossmann RE, Keller F.
    Thromb Haemost; 1997 Dec 21; 78(6):1480-3. PubMed ID: 9423798
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  • 17. Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency.
    van Boven HH, Reitsma PH, Rosendaal FR, Bayston TA, Chowdhury V, Bauer KA, Scharrer I, Conard J, Lane DA.
    Thromb Haemost; 1996 Mar 21; 75(3):417-21. PubMed ID: 8701400
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  • 18. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
    Ireland H, Thompson E, Lane DA.
    Thromb Haemost; 1996 Dec 21; 76(6):867-73. PubMed ID: 8972002
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  • 19. Factor V Leiden: an additional risk factor for thrombosis in protein S deficient families?
    Koeleman BP, van Rumpt D, Hamulyák K, Reitsma PH, Bertina RM.
    Thromb Haemost; 1995 Aug 21; 74(2):580-3. PubMed ID: 8584987
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  • 20. Risk of pregnancy-related venous thrombosis in carriers of severe inherited thrombophilia.
    Martinelli I, Legnani C, Bucciarelli P, Grandone E, De Stefano V, Mannucci PM.
    Thromb Haemost; 2001 Sep 21; 86(3):800-3. PubMed ID: 11583310
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