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Volumn 92, Issue 5, 2004, Pages 1157-1158

Liver transplantation for type I primary hyperoxaluria as a cure for combined thrombophilia

Author keywords

[No Author keywords available]

Indexed keywords

APC PROTEIN; BLOOD CLOTTING FACTOR 5 LEIDEN; CALCIUM OXALATE; LOW MOLECULAR WEIGHT HEPARIN; ORAL CONTRACEPTIVE AGENT; PROTHROMBIN;

EID: 9144256110     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1614295     Document Type: Article
Times cited : (3)

References (11)
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  • 3
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    • Primary hyperoxaluria: Simultaneous combined liver and kidney transplantation from a living related donor
    • Astarcioglu I, Karademir S, Gulay H, et al. Primary hyperoxaluria: simultaneous combined liver and kidney transplantation from a living related donor. Liver Transpl 2003; 9: 433-6.
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    • Astarcioglu, I.1    Karademir, S.2    Gulay, H.3
  • 4
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    • Inherited deficiencies of coagulation factors
    • McGraw-Hill
    • Beutler E, Lichtman MA, Coller BS, et al. Inherited deficiencies of coagulation factors. In: Williams Hematology. McGraw-Hill 2001; 1617-38.
    • (2001) Williams Hematology , pp. 1617-1638
    • Beutler, E.1    Lichtman, M.A.2    Coller, B.S.3
  • 5
    • 0034840147 scopus 로고    scopus 로고
    • Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism - Pooled analysis of 8 case-control studies including 2310 cases and 3204 controls
    • Emmerich J, Rosendaal FR, Cattaneo M, et al. Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism - pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Thromb Haemost. 2001; 86: 809-16.
    • (2001) Thromb. Haemost. , vol.86 , pp. 809-816
    • Emmerich, J.1    Rosendaal, F.R.2    Cattaneo, M.3
  • 6
    • 0033812671 scopus 로고    scopus 로고
    • Successful liver transplantation in a patient with Budd-Chiari syndrome caused by homozygous factor V Leiden
    • Tan HP, Markowitz JS, Maley WR, et al. Successful liver transplantation in a patient with Budd-Chiari syndrome caused by homozygous factor V Leiden. Liver Transpl 2000; 6: 654-6.
    • (2000) Liver Transpl. , vol.6 , pp. 654-656
    • Tan, H.P.1    Markowitz, J.S.2    Maley, W.R.3
  • 7
    • 0041561261 scopus 로고    scopus 로고
    • Recurrent deep-vein thrombosis based on homozygous factor V Leiden mutation acquired after liver transplantation
    • Willems M, Sterneck M, Langer F, et al. Recurrent deep-vein thrombosis based on homozygous factor V Leiden mutation acquired after liver transplantation. Liver Transpl 2003; 9: 870-3.
    • (2003) Liver Transpl. , vol.9 , pp. 870-873
    • Willems, M.1    Sterneck, M.2    Langer, F.3
  • 8
    • 0031962947 scopus 로고    scopus 로고
    • Donor factor V Leiden mutation and vascular thrombosis following liver transplantation
    • Hirshfield G, Collier JD, Brown K, et al. Donor factor V Leiden mutation and vascular thrombosis following liver transplantation. Liver Transpl Surg 1998; 4: 58-61.
    • (1998) Liver Transpl. Surg. , vol.4 , pp. 58-61
    • Hirshfield, G.1    Collier, J.D.2    Brown, K.3
  • 9
    • 0036020467 scopus 로고    scopus 로고
    • A 9-year retrospective assessment of laboratory testing for activated protein C resistance: Evolution of a novel approach to thrombophilia investigations
    • Favaloro EJ, Orsag I, Bukuya M, et al. A 9-year retrospective assessment of laboratory testing for activated protein C resistance: evolution of a novel approach to thrombophilia investigations. Pathology 2002; 34: 348-55.
    • (2002) Pathology , vol.34 , pp. 348-355
    • Favaloro, E.J.1    Orsag, I.2    Bukuya, M.3
  • 10
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    • Coagulation factor II activity determination is not useful as a screening tool for the G20210A prothrombin gene allele
    • Gruenewald M, Germowitz A, Beneke H, et al. Coagulation factor II activity determination is not useful as a screening tool for the G20210A prothrombin gene allele. Thromb Haemost 2000; 84: 141-2.
    • (2000) Thromb. Haemost. , vol.84 , pp. 141-142
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  • 11
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    • Poort SR, Rosendaal FR, Reitsma PH, et al. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-703.
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    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.