This is a fascinating time for haemophilia and other congenital bleeding diseases, as recently reflected by major therapeutic innovations, such as the newly developed longer‐acting clotting factor concentrates, promising so‐called disruptive therapies, along with the lately reported successes of gene therapy trials in both haemophilia A and haemophilia B. These therapeutic innovations will likely and significantly impact the management and care of persons with haemophilia or other inherited bleeding diseases around the world. [...
Hemophilia comprises two distinct genetic disorders caused by missing or defective clotting factor V...
Patients with haemophilia A (HA) or B (HB) experience spontaneous limb- or life-threatening bleeding...
Hemophilia is an inherited bleeding disorder caused by the lack of a protein necessary for blood clo...
Hemophilia A (HA) and B (HB) are X-linked bleeding disorders caused by mutations in the F8 or F9 gen...
Haemophilia A and B are hereditary haemorrhagic disorders characterised by deficiency or dysfunction...
Haemophilia is a rare bleeding disorder, caused by a mutation in the genes for factor VIII (Haemoph...
Comprehensive, integrated care provided by a multi-disciplinary team of experts improves outcomes an...
Hemophilia is a genetic disease caused by a deficiency of one of the coagulation proteins. The term ...
Hemophilia unfortunately a less attracted disease for researchers compared to other life threatening...
The last two decades has seen significant progress in the treatment of hemophilia A. The developmen...
Hemophilia treatment is entering a new phase, with the exciting possibility of gene therapy promisin...
Hemophilia is a single gene disorder and as a genetical coagulation system problem it is a life-long...
Better access to haemophilia treatment and care is currently changing the life of a great many patie...
With liver-directed gene therapy, congenital haemophilia has the potential to progress from an incur...
Historically, the bleeding episodes in subjects with coagulation disorders were treated with substit...
Hemophilia comprises two distinct genetic disorders caused by missing or defective clotting factor V...
Patients with haemophilia A (HA) or B (HB) experience spontaneous limb- or life-threatening bleeding...
Hemophilia is an inherited bleeding disorder caused by the lack of a protein necessary for blood clo...
Hemophilia A (HA) and B (HB) are X-linked bleeding disorders caused by mutations in the F8 or F9 gen...
Haemophilia A and B are hereditary haemorrhagic disorders characterised by deficiency or dysfunction...
Haemophilia is a rare bleeding disorder, caused by a mutation in the genes for factor VIII (Haemoph...
Comprehensive, integrated care provided by a multi-disciplinary team of experts improves outcomes an...
Hemophilia is a genetic disease caused by a deficiency of one of the coagulation proteins. The term ...
Hemophilia unfortunately a less attracted disease for researchers compared to other life threatening...
The last two decades has seen significant progress in the treatment of hemophilia A. The developmen...
Hemophilia treatment is entering a new phase, with the exciting possibility of gene therapy promisin...
Hemophilia is a single gene disorder and as a genetical coagulation system problem it is a life-long...
Better access to haemophilia treatment and care is currently changing the life of a great many patie...
With liver-directed gene therapy, congenital haemophilia has the potential to progress from an incur...
Historically, the bleeding episodes in subjects with coagulation disorders were treated with substit...
Hemophilia comprises two distinct genetic disorders caused by missing or defective clotting factor V...
Patients with haemophilia A (HA) or B (HB) experience spontaneous limb- or life-threatening bleeding...
Hemophilia is an inherited bleeding disorder caused by the lack of a protein necessary for blood clo...