and fibrinolysis factors Patients with severe haemophilia A or B are at high risk of recurrent bleeding and require treatment with procoagulant fac-tors, such as factor VIIa or factor IX. Unfor-tunately, the half-life of the recombinant forms of these proteins is rather short (2–3 hours). The generation of genetically fused constructs with albumin, as reported by Weimer et al. (1) and Metzner et al. (2), not only prolongs the half-life of the coagu-lation proteins in animal models, but they also express biological activity comparable to the unmodified counterparts or to pro-teins chemically modified by poly-ethy
Haemophilia A and haemophilia B are congenital X-linked bleeding disorders caused by deficiency of c...
Haemophilia A (HA) and B (HB) as well as factor VII (FVII) or X (FX) deficiencies are well-character...
quent infusions of factor IX (FIX) to pro-phylax against bleeding episodes. Hemo-philia B management...
Hemophilia is a genetic disease caused by a deficiency of one of the coagulation proteins. The term ...
The development of a new generation of coagulation factors with improved pharmacokinetic profile wil...
The short half-life of coagulation factor IX (FIX) for haemophilia B (HB) therapy has been prolonged...
Hemophilias A and B are X chromosome-linked bleeding disorders, which are mainly treated by repeated...
There are two main bioengineering approaches to extending the half-life of factor (F)VIII or FIX pro...
Moniba Nazeef,1,2 John P Sheehan1,2 1Department of Medicine, Division of Hematology/Oncology, 2UW Ca...
Current management of hemophilia B entails multiple weekly infusions of factor IX (FIX) to prevent b...
Background: Haemophilia A is an X-linked bleeding disorder resulting from dysregulation of clotting ...
Haemophilia A and haemophilia B are congenital X-linked bleeding disorders caused by deficiency of c...
Treatment of congenital haemophilia with factor VIII and IX concentrates often requires frequent inf...
Marcus E Carr,1,2 Bartholomew J Tortella3,4 1Robert Wood Johnson Medical School, Rutgers University,...
Bleeding inhemophilia is the result of factorVIII/IXdeficiencywith corresponding reduced thrombinpro...
Haemophilia A and haemophilia B are congenital X-linked bleeding disorders caused by deficiency of c...
Haemophilia A (HA) and B (HB) as well as factor VII (FVII) or X (FX) deficiencies are well-character...
quent infusions of factor IX (FIX) to pro-phylax against bleeding episodes. Hemo-philia B management...
Hemophilia is a genetic disease caused by a deficiency of one of the coagulation proteins. The term ...
The development of a new generation of coagulation factors with improved pharmacokinetic profile wil...
The short half-life of coagulation factor IX (FIX) for haemophilia B (HB) therapy has been prolonged...
Hemophilias A and B are X chromosome-linked bleeding disorders, which are mainly treated by repeated...
There are two main bioengineering approaches to extending the half-life of factor (F)VIII or FIX pro...
Moniba Nazeef,1,2 John P Sheehan1,2 1Department of Medicine, Division of Hematology/Oncology, 2UW Ca...
Current management of hemophilia B entails multiple weekly infusions of factor IX (FIX) to prevent b...
Background: Haemophilia A is an X-linked bleeding disorder resulting from dysregulation of clotting ...
Haemophilia A and haemophilia B are congenital X-linked bleeding disorders caused by deficiency of c...
Treatment of congenital haemophilia with factor VIII and IX concentrates often requires frequent inf...
Marcus E Carr,1,2 Bartholomew J Tortella3,4 1Robert Wood Johnson Medical School, Rutgers University,...
Bleeding inhemophilia is the result of factorVIII/IXdeficiencywith corresponding reduced thrombinpro...
Haemophilia A and haemophilia B are congenital X-linked bleeding disorders caused by deficiency of c...
Haemophilia A (HA) and B (HB) as well as factor VII (FVII) or X (FX) deficiencies are well-character...
quent infusions of factor IX (FIX) to pro-phylax against bleeding episodes. Hemo-philia B management...