By W. Schramm, H. Krebs (auth.), Professor Dr. med. Inge Scharrer, Professor Dr. med. Wolfgang Schramm (eds.)
This booklet includes the contribution to the thirty fifth Hemophilia Symposium, Hamburg 2004. the most issues are epidemiology, probability of infections and inhibitors in hemophilia, power hemophilic synovitis and long term result of orthopedic therapy, laboratory diagnostics and pediatric hemostaseology. the quantity is rounded off via various loose papers and posters on hemophilia and hemorrhagic issues and inhibitors in hemophilia.
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Additional info for 35th Hemophilia Symposium: Hamburg 2004
Compared to the data of the previous surveys these are relative consistent findings. e. below 2% and above 2%, is similar in patients with hemophilia A (51,7/48,3%) and B (46,4/53,6%) as shown in Table 2. 22,6% of patients with von Willebrand disease showed Ristocetin co-factor levels below 30% as demonstrated in Table 2. Inhibitors In 3,5% (134) of the patients with hemophilia A and in 2,4% (16) of the patients with hemophilia B an inhibitor was found (see Table 2). These findings correspond to international large-scale prevalence studies and registry data indicating that the prevalence of inhibitors in the hemophiliac A population overall is up to 5% .
The aims of the prize are laid down in the statutes of the foundation: The foundation serves to promote clinical research in the area of chronic bleeding diseases, in particular, hemophilia and related congenital clotting disorders. It follows exclusively and directly charitable purposes and awards the prize for outstanding scientific research. The board of trustees responsible for awarding the prize is made up of seven independent scientists. This year there were four applicants for the prize.
Giangrande granted which will permit the target of recombinant for all to be reached by April 2005. It is a fact that physicians in hemophilia centers were notified in 1997 and again in 2000 by the Department of Health in the UK that patients diagnosed with vCJD had been blood donors and contributed to pools used to manufacture a number of specified batches of coagulation factor concentrates. However, the official advice at the time was not to inform patients and no special precautions were advocated .
35th Hemophilia Symposium: Hamburg 2004 by W. Schramm, H. Krebs (auth.), Professor Dr. med. Inge Scharrer, Professor Dr. med. Wolfgang Schramm (eds.)