A therapeutic alternative for haemophiliacs with inhibitors
- 1 June 1992
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 81 (6-7) , 564-565
- https://doi.org/10.1111/j.1651-2227.1992.tb12297.x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- PROLONGED RECOMBINANT ACTIVATED FACTOR VII (rFVIIa) TREATMENT FOR SEVERE BLEEDING IN A FACTOR‐IX‐DEFICIENT PATIENT WITH AN INHIBITORBritish Journal of Haematology, 1991
- Mechanism by which recombinant factor VIIa shortens the aPTT: Activation of factor X in the absence of tissue factorThrombosis Research, 1989
- Use of recombinant activated factor VII for treatment of a retropharyngeal hemorrhage in a hemophilic patient with a high titer inhibitorAmerican Journal of Hematology, 1989
- Clinical Experience with Human Plasma-Derived Factor VIla in Patients with Hemophilia A and High Titer InhibitorsPathophysiology of Haemostasis and Thrombosis, 1989
- SUCCESSFUL USE OF RECOMBINANT FACTOR VIIa IN PATIENT WITH SEVERE HAEMOPHILIA A DURING SYNOVECTOMYThe Lancet, 1988
- Use of human factor VIIa in the treatment of two hemophilia A patients with high-titer inhibitors.Journal of Clinical Investigation, 1983
- A Survey of 215 Non-Hemophilic Patients with Inhibitors to Factor VIIIThrombosis and Haemostasis, 1981