Results 121 to 130 of about 1,795 (145)
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Emicizumab for hemophilia A without inhibitors

Expert Review of Hematology, 2019
Introduction: Hemophilia A (HA) is an inherited bleeding disorder that, if not properly treated, is associated with debilitating joint damage due to recurrent hemarthroses as well as life-threatening bleeds including intracranial hemorrhage. For decades, the only method to prevent bleeding events was to infuse factor (F) VIII concentrates intravenously
Lorraine Cafuir   +3 more
openaire   +2 more sources

Emicizumab: A Review in Haemophilia A

Drugs, 2019
Emicizumab (Hemlibra®), a recombinant, humanized, bispecific monoclonal antibody, restores the function of missing activated factor VIII (FVIII) by bridging FIXa and FX to facilitate effective haemostasis in patients with haemophilia A. Subcutaneous emicizumab is approved in several countries, including in the USA and Japan, for the routine prophylaxis
openaire   +2 more sources

Emicizumab in Children with Severe Hemophilia A

Indian Journal of Pediatrics
To assess the effectiveness and tolerability of emicizumab prophylaxis in hemophilia A (HA). Emicizumab is a novel therapeutic drug which is the first and only non-factor replacement agent licensed for use in people with HA.Pediatric patients aged 1 mo to 12 y with severe HA and frequent / life threatening bleeding events, with or without coagulation ...
Usha Rani Thota   +3 more
openaire   +2 more sources

Emicizumab for the prevention of bleeds in hemophilia A

Expert Opinion on Biological Therapy, 2019
Introduction: The management of hemophilia A with and without inhibitors is challenging with high treatment burden of prophylactic regimens, musculoskeletal complications, poor treatment compliance, poor venous access and therapies with suboptimal levels.
openaire   +2 more sources

Functional determination of emicizumab in presence of factor VIII activity

Journal of Thrombosis and Haemostasis, 2023
Bernd Pötzsch   +2 more
exaly  

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