Titlebook: 32nd Hemophilia Symposium Hamburg 2001; Inge Scharrer,Wolfgang Schramm Conference proceedings 2003 Springer-Verlag Berlin Heidelberg 2003

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978-3-540-43884-7Springer-Verlag Berlin Heidelberg 2003

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Vijay K. Madisetti,Chonlameth Arpikanondtint bleedings and hemophilic arthropathy in hemophilia patients, a long-term prophylactic therapy with factor VIII or IX concentrates has been suggested. This coagulation factor substitution can be complicated by the development of antibodies against factor VIII or IX (sc. inhibitors).

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Monetary and Financial RequirementsEach year the Institute of Social Medicine of Vienna (ISM) organizes the annual survey of the Austrian Hemophilia Centers where the anonymous questionnaires from all collaborating centers are collected and analyzed.

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Platform-Centric SoC Design Methodology,rinolysis predispose to thromboembolic events [1–5]. The factor V (FV) G1691A Mutation and the prothrombin (Fil) G20210A variant appear to be relevant not only in adult thromboembolism. However, due to the low incidence of thromboembolic events in childhood, the role of hereditary prothrombotic risk