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Journal Abstract Search


255 related items for PubMed ID: 25039884

  • 21. Venous thromboembolism in children: details of 46 cases based on a follow-up survey of POSNA members.
    Sabharwal S, Zhao C, Passanante M.
    J Pediatr Orthop; 2013; 33(7):768-74. PubMed ID: 23812156
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  • 23. Risk factors and recurrence rate of primary deep vein thrombosis of the upper extremities.
    Martinelli I, Battaglioli T, Bucciarelli P, Passamonti SM, Mannucci PM.
    Circulation; 2004 Aug 03; 110(5):566-70. PubMed ID: 15262837
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  • 24. A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency.
    Zöller B, García de Frutos P, Dahlbäck B.
    Thromb Haemost; 1998 Apr 03; 79(4):802-7. PubMed ID: 9569196
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  • 25. Thrombophilia in childhood: to test or not to test.
    Heleen van Ommen C, Middeldorp S.
    Semin Thromb Hemost; 2011 Oct 03; 37(7):794-801. PubMed ID: 22187402
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  • 27. The prevalence of thrombophilia and venous thromboembolism in total knee arthroplasty.
    Chotanaphuti T, Ongnamthip P, Silpipat S, Foojareonyos T, Roschan S, Reumthantong A.
    J Med Assoc Thai; 2007 Jul 03; 90(7):1342-7. PubMed ID: 17710975
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  • 28. Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhood.
    Nowak-Göttl U, Junker R, Hartmeier M, Koch HG, Münchow N, Assmann G, von Eckardstein A.
    Circulation; 1999 Aug 17; 100(7):743-8. PubMed ID: 10449697
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  • 29. Inherited thrombophilic risk factors in a large cohort of individuals referred to Italian thrombophilia centers: distinct roles in different clinical settings.
    Margaglione M, Brancaccio V, Ciampa A, Papa ML, Grandone E, Di Minno G.
    Haematologica; 2001 Jun 17; 86(6):634-9. PubMed ID: 11418373
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  • 30. The John Charnley Award: heritable thrombophilia and development of thromboembolic disease after total hip arthroplasty.
    Salvati EA, Della Valle AG, Westrich GH, Rana AJ, Specht L, Weksler BB, Wang P, Glueck CJ.
    Clin Orthop Relat Res; 2005 Dec 17; 441():40-55. PubMed ID: 16330983
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  • 31. Purpura fulminans in congenital protein C deficiency successfully treated with fresh frozen plasma and thrombomodulin.
    Hayami T, Yamaguchi A, Kato T, Tanaka T, Nishizawa Y, Yanagi T, Taga T, Matsumoto S, Uchiumi T, Fujimoto N.
    J Dermatol; 2018 Jun 17; 45(6):e165-e166. PubMed ID: 29265490
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  • 36. [Rare thrombophilic states].
    Emmerich J.
    Rev Med Interne; 2008 Jun 17; 29(6):482-5. PubMed ID: 18394759
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  • 37. Hereditary and acquired thrombophilia in patients with upper extremity deep-vein thrombosis. Results from the MAISTHRO registry.
    Linnemann B, Meister F, Schwonberg J, Schindewolf M, Zgouras D, Lindhoff-Last E, MAISTHRO registry.
    Thromb Haemost; 2008 Sep 17; 100(3):440-6. PubMed ID: 18766260
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  • 38. Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism.
    Kuhle S, Lane DA, Jochmanns K, Male C, Quehenberger P, Lechner K, Pabinger I.
    Thromb Haemost; 2001 Oct 17; 86(4):1007-11. PubMed ID: 11686316
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