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Journal Abstract Search

389 related items for PubMed ID: 11583329

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  • 3. 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; 86(3):800-3. PubMed ID: 11583310
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  • 5. Incidence of venous thromboembolism in families with inherited thrombophilia.
    Simioni P, Sanson BJ, Prandoni P, Tormene D, Friederich PW, Girolami B, Gavasso S, Huisman MV, Büller HR, Wouter ten Cate J, Girolami A, Prins MH.
    Thromb Haemost; 1999 Feb; 81(2):198-202. PubMed ID: 10063991
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  • 6. Thrombophilia as a multigenic disease.
    Zöller B, García de Frutos P, Hillarp A, Dahlbäck B.
    Haematologica; 1999 Jan; 84(1):59-70. PubMed ID: 10091393
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  • 7. Risk factors for clinical manifestations in carriers of Factor V Leiden and prothrombin gene mutations.
    DeSancho MT, Berlus N, Christos PJ, Rand J.
    Blood Coagul Fibrinolysis; 2010 Jan; 21(1):11-5. PubMed ID: 19474699
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  • 8. Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism.
    De Stefano V, Casorelli I, Rossi E, Zappacosta B, Leone G.
    Semin Thromb Hemost; 2000 Jan; 26(3):305-11. PubMed ID: 11011848
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  • 9. The risk of recurrent venous thromboembolism in patients with inherited deficiency of natural anticoagulants antithrombin, protein C and protein S.
    De Stefano V, Simioni P, Rossi E, Tormene D, Za T, Pagnan A, Leone G.
    Haematologica; 2006 May; 91(5):695-8. PubMed ID: 16670075
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  • 12. [Thrombophilias associated with cerebral venous thrombosis].
    Schlück E, Rodier G, Derouiche F, Bronner P, Boulay C, Courtois S, Cohen E.
    Rev Neurol (Paris); 2002 May; 158(5 Pt 1):543-52. PubMed ID: 12072822
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  • 13. Thrombophilia: a genetic predisposition to thrombosis.
    Sacher RA.
    Trans Am Clin Climatol Assoc; 1999 May; 110():51-60; discussion 60-1. PubMed ID: 10344006
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  • 14. Foetal growth restriction in children with prothrombotic risk factors.
    von Kries R, Junker R, Oberle D, Kosch A, Nowak-Göttl U.
    Thromb Haemost; 2001 Oct; 86(4):1012-6. PubMed ID: 11686317
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  • 15. A rebuttal: Counseling pregnant women with factor V Leiden homozygosity: use absolute instead of relative risks.
    Middeldorp S, van der Meer J, Hamulyák K, Büller HR.
    Thromb Haemost; 2002 Feb; 87(2):360-1; author reply 361. PubMed ID: 11858509
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  • 16. Hemostatic risk factors and arterial thrombotic disease.
    Reiner AP, Siscovick DS, Rosendaal FR.
    Thromb Haemost; 2001 Apr; 85(4):584-95. PubMed ID: 11341490
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  • 17. Primary upper-extremity deep vein thrombosis: high prevalence of thrombophilic defects.
    Hendler MF, Meschengieser SS, Blanco AN, Alberto MF, Salviú MJ, Gennari L, Lazzari MA.
    Am J Hematol; 2004 Aug; 76(4):330-7. PubMed ID: 15282664
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  • 18. Risk of recurrent venous thrombosis in children with combined prothrombotic risk factors.
    Nowak-Göttl U, Junker R, Kreuz W, von Eckardstein A, Kosch A, Nohe N, Schobess R, Ehrenforth S, Childhood Thrombophilia Study Group.
    Blood; 2001 Feb 15; 97(4):858-62. PubMed ID: 11159508
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  • 19. Multiplex PCR for one-step determination of the G20210A variation and the factor V Leiden mutation by denaturing gradient gel electrophoresis (DGGE).
    Patri S, Salmeron S, Caillon M, Kitzis A, Chomel JC.
    Thromb Haemost; 1999 Feb 15; 81(2):313-4. PubMed ID: 10064013
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  • 20. Inherited prothrombotic risk factors in Turkish children with acute lymphoblastic leukemia: significance of concomitant genetic mutation.
    Torun YA, Patiroglu T, Ozdemir MA, Ozkul Y, Ekici A, Karakukcu M.
    Clin Appl Thromb Hemost; 2012 Feb 15; 18(2):218-21. PubMed ID: 21873357
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