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Thromb Haemost 2004; 92(05): 1157-1158
DOI: 10.1055/s-0037-1614295
DOI: 10.1055/s-0037-1614295
Case Report
Liver transplantation for type 1 primary hyperoxaluria as a cure for combined thrombophilia
Further Information
Publication History
Received
15 June 2004
Accepted after revision
08 August 2004
Publication Date:
14 December 2017 (online)
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References
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- 3 Astarcioglu I, Karademir S, Gulay H. et al. Primary hyperoxaluria: simultaneous combined liver and kidney transplantation from a living related donor. Liver Transpl 2003; 09: 433-6.
- 4 Beutler E, Lichtman MA, Coller BS. et al. Inherited deficiencies of coagulation factors. In: Williams Hematology. McGraw-Hill; 2001: 1617-38.
- 5 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.
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- 10 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.
- 11 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.