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Journal Abstract Search

294 related items for PubMed ID: 8047373

  • 1. Protein C and S deficiency, thrombophilia, and hypofibrinolysis: pathophysiologic causes of Legg-Perthes disease.
    Glueck CJ, Glueck HI, Greenfield D, Freiberg R, Kahn A, Hamer T, Stroop D, Tracy T.
    Pediatr Res; 1994 Apr; 35(4 Pt 1):383-8. PubMed ID: 8047373
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  • 2. Secondhand smoke, hypofibrinolysis, and Legg-Perthes disease.
    Glueck CJ, Freiberg RA, Crawford A, Gruppo R, Roy D, Tracy T, Sieve-Smith L, Wang P.
    Clin Orthop Relat Res; 1998 Jul; (352):159-67. PubMed ID: 9678044
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  • 4. Association of antithrombotic factor deficiencies and hypofibrinolysis with Legg-Perthes disease.
    Glueck CJ, Crawford A, Roy D, Freiberg R, Glueck H, Stroop D.
    J Bone Joint Surg Am; 1996 Jan; 78(1):3-13. PubMed ID: 8550676
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  • 5. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].
    Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M.
    Srp Arh Celok Lek; 1999 Jan; 127(1-2):21-7. PubMed ID: 10377836
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  • 11. Laboratory screening of inherited thrombotic syndromes.
    Mannucci PM, Tripodi A.
    Thromb Haemost; 1987 Jun 03; 57(3):247-51. PubMed ID: 3116699
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  • 12. Familial high plasminogen activator inhibitor with hypofibrinolysis, a new pathophysiologic cause of osteonecrosis?
    Glueck CJ, Glueck HI, Mieczkowski L, Tracy T, Speirs J, Stroop D.
    Thromb Haemost; 1993 May 03; 69(5):460-5. PubMed ID: 8322268
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  • 13. 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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  • 14. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis.
    Gladson CL, Scharrer I, Hach V, Beck KH, Griffin JH.
    Thromb Haemost; 1988 Feb 25; 59(1):18-22. PubMed ID: 2966450
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  • 15. High incidence of thrombophilia detected in Chinese patients with venous thrombosis.
    Liu HW, Kwong YL, Bourke C, Lam CK, Lie AK, Wei D, Chan LC.
    Thromb Haemost; 1994 Apr 25; 71(4):416-9. PubMed ID: 8052955
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  • 18. High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin.
    Brouwer JL, Lijfering WM, Ten Kate MK, Kluin-Nelemans HC, Veeger NJ, van der Meer J.
    Thromb Haemost; 2009 Jan 25; 101(1):93-9. PubMed ID: 19132194
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  • 19. Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism--results of the Spanish Multicentric Study on Thrombophilia (EMET-Study).
    Mateo J, Oliver A, Borrell M, Sala N, Fontcuberta J.
    Thromb Haemost; 1997 Mar 25; 77(3):444-51. PubMed ID: 9065991
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  • 20. Fibrinolysis, antithrombin III, and protein C in neonates during cardiac operations.
    Petăjă J, Peltola K, Sairanen H, Leijala M, Kekomäki R, Vahtera E, Siimes MA.
    J Thorac Cardiovasc Surg; 1996 Sep 25; 112(3):665-71. PubMed ID: 8800154
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