Hemophilia is a single gene disorder and as a genetical coagulation system problem it is a life-long bleeding disorder. Even though routine treatment modalities as plasma-derived and then recombinant factor concentrates available for last 50 years, unmet needs is continuing for hemophilia therapy. Gold standart treatment is regularly prophylactic FVIII/FIX infusions. However, life-long and frequent intra-venous infusions become medical burden for patients and families. New agents as enhanced half-life (EHL) factor concentrates and non-factor therapies which are able to be used subcutaneously are very hopeful. In this review, EHL factor concentrates, FVIII mimetic agents and re-balancing therapies will be discussed. Although celluler gene th...
In persons with congenital severe hemophilia A (HA) living in high-income countries, twice weekly in...
In contrast to other diverse therapies for the X-linked bleeding disorder hemophilia that are curren...
Haemophilia therapy has undergone very rapid evolution in the last 10 years. The major limitation of...
The last two decades has seen significant progress in the treatment of hemophilia A. The developmen...
Marcus E Carr,1,2 Bartholomew J Tortella3,4 1Robert Wood Johnson Medical School, Rutgers University,...
Historically, the standard of care for hemophilia A has been intravenous administration of exogenous...
Advancements and debacles have characterized hemophilia treatment over the past 50 years. The 1970s ...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Hemophilia A (HA) and B (HB) are X-linked bleeding disorders caused by mutations in the F8 or F9 gen...
Hemophilia treatment is entering a new phase, with the exciting possibility of gene therapy promisin...
Hemophilia A is an inherited insufficiency of Factor VIII (FVIII), one of the critical clotting fact...
Hemophilia A is an inherited insufficiency of Factor VIII (FVIII), one of the critical clotting fact...
Hemophilia A (HA) and B (HB) are X-linked bleeding disorders caused by mutations in the F8 or F9 gen...
In persons with congenital severe hemophilia A (HA) living in high-income countries, twice weekly in...
In contrast to other diverse therapies for the X-linked bleeding disorder hemophilia that are curren...
Haemophilia therapy has undergone very rapid evolution in the last 10 years. The major limitation of...
The last two decades has seen significant progress in the treatment of hemophilia A. The developmen...
Marcus E Carr,1,2 Bartholomew J Tortella3,4 1Robert Wood Johnson Medical School, Rutgers University,...
Historically, the standard of care for hemophilia A has been intravenous administration of exogenous...
Advancements and debacles have characterized hemophilia treatment over the past 50 years. The 1970s ...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Hemophilia A (HA) and B (HB) are X-linked bleeding disorders caused by mutations in the F8 or F9 gen...
Hemophilia treatment is entering a new phase, with the exciting possibility of gene therapy promisin...
Hemophilia A is an inherited insufficiency of Factor VIII (FVIII), one of the critical clotting fact...
Hemophilia A is an inherited insufficiency of Factor VIII (FVIII), one of the critical clotting fact...
Hemophilia A (HA) and B (HB) are X-linked bleeding disorders caused by mutations in the F8 or F9 gen...
In persons with congenital severe hemophilia A (HA) living in high-income countries, twice weekly in...
In contrast to other diverse therapies for the X-linked bleeding disorder hemophilia that are curren...
Haemophilia therapy has undergone very rapid evolution in the last 10 years. The major limitation of...