Regulation of FVIII-specific immunity in Hemophilia A mice
The major complication of Hemophilia A treatment is the formation of inhibitors that neutralize the administered FVIII. Immune tolerance induction (ITI) is the most frequently used therapy in order to establish long-lasting tolerance towards FVIII in ...
Jurado Mestre, Blanca
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Discovery and development of a bispecific antibody for the treatment of hemophilia. [PDF]
Pao W.
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Kunihiro Hattori, Tomoyuki Igawa, and Takehisa Kitazawa share Lasker Award honors for revolutionary hemophilia A therapy. [PDF]
Flaumenhaft R.
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A Novel Complete F8 Tandem Duplication Causing Elevated Factor VIII Activity and Associated with Venous Thromboembolism. [PDF]
Mao Y +6 more
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Tissue Factor/Factor XIa Dual-activated Thrombin Generation is Able to Reliably Measure Thrombin Generation at All Hemophilia A Disease Severities. [PDF]
van de Berg TW +9 more
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Structural basis for membrane binding by coagulation factors V and VIII and their specificity for phosphatidylserine-containing membranes. [PDF]
Kolyadko VN +3 more
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Plasma emicizumab concentrations and bleeding rates in children and adults with severe hemophilia A. [PDF]
Teitel J +6 more
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Maternal microchimerism accelerates immune tolerance induction to factor VIII in children with hemophilia A and FVIII inhibitors. [PDF]
Li Z +15 more
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Acquired hemophilia a caused by complicated urinary tract infection due to flavobacterium odoratum: A case report and literature review. [PDF]
Chen D, Yuan P, Ren M.
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Die heutige Standardversorgung für Patienten mit der Blutgerinnungsstörung Hämophilie A umfasst eine rekombinante Proteinersatztherapie des fehlenden oder defekten Faktor VIII (FVIII).
Weyrer, Franziska
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