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Titlebook: 33rd Hemophilia Symposium; Hamburg 2002 Inge Scharrer,Wolfgang Schramm Conference proceedings 2004 Springer-Verlag Berlin Heidelberg 2004 H

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楼主: Maculate
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A Polynomial Approach to Linear Algebray episodic bolus infusions (BI) the CI had several advantages:.Steady level of missing coagulation factor, avoiding of unnecessary high peaks of FVIII, saving of 30% FVIII concentrate and reduction in treatment costs [.]. Reports of the occurrence of an inhibitor after treatment with CI have raised concerns about this method of factor application.
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https://doi.org/10.1007/978-1-349-08277-3ated coagulation factors that are intended to achieve hemostasis by bypassing FVIII and independently of FVIII [., .]. Activated prothrombin complex concentrates such as FEIBA contain vitamin-K-dependent coagulation factor zymogens and a small amount of their activated forms (.).
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Assessing the BWB partial privatisation,970s Professor Landbeck began to survey annually hemophiliacs living at that time in West Germany for causes of death and the prevalence of diseases. This was carried on till today, so that our actual insights rest upon a broad database.However data quality could be much more improved in future. Esp
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https://doi.org/10.1007/978-3-658-11765-8ivation mechanism and a precondition for the modification of recombinant coagulation factors to reduce their immunogenicity would be the exact localization of immuno-dominant epitopes. To investigate whether such epitopes could be identified using a random peptide phage display library, FVIII antibo
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https://doi.org/10.1007/978-3-658-11765-8ilia is a rare event, with an incidence of 0.2–1 per million per year and a mortality between 6% and 22%. In the majority of patients no cause can be identified. Up to 50% of the patients with autoantibodies against factor VIII are associated with autoimmune diseases, malignancies, drugs, pregnancie
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Contemplating a Repronational Portrait circumstance is the result of preventive treatment of the underlying bleeding disorder and immediate curative treatment of any bleeding on the basis of ready access to sufficient quantities of coagulation factor concentrates. With no restrictions on their freedom of movement, young hemophiliacs of
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