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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 18, 2015
Changes in bleeding patterns in von Willebrand disease after institution of long-term replacement therapy: results from the von Willebrand Disease Prophylaxis NetworkElena Holm, Thomas C Abshire, Joel Bowen, et al.Thrombosis and Haemostasis|December 7, 2017
Risk Factors for the Progression from Low to High Titres in 260 Children with Severe Haemophilia A and Newly Developed InhibitorsMaria Elisa Mancuso, Kathelijn Fischer, Elena Santagostino, et al.British Journal of Haematology|July 13, 2017
Intracranial haemorrhage in children and adolescents with severe haemophilia A or B - the impact of prophylactic treatmentNadine G Andersson, Günter Auerswald, Chris Barnes, et al.Blood|April 5, 2013
Intensity of factor VIII treatment and inhibitor development in children with severe hemophilia A: the RODIN studySamantha C Gouw, H Marijke van den Berg, Kathelijn Fischer, et al.European Journal of Haematology|July 13, 2023
Simoctocog alfa (Nuwiq®) in previously untreated patients with severe haemophilia A-Final efficacy and safety results from the NuProtect studyMary Mathias, Aby Abraham, Mark J Belletrutti, et al.Thrombosis and Haemostasis|February 13, 2021
Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect StudyRi J Liesner, Aby Abraham, Carmen Altisent, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 27, 2022
Eptacog beta efficacy and safety in the treatment and control of bleeding in paediatric subjects (<12 years) with haemophilia A or B with inhibitorsSteven W Pipe, Cédric Hermans, Meera Chitlur, et al.Research and Practice in Thrombosis and Haemostasis|November 19, 2024
Prediction of the chance of successful immune tolerance induction in persons with severe hemophilia A and inhibitors: a clinical prediction modelIlja Oomen, Amal Abdi, Ricardo M Camelo, et al.Research and Practice in Thrombosis and Haemostasis|November 17, 2025
Large deletions in the <i>F8</i> gene predict immune tolerance induction failure in people with severe hemophilia AIlja Oomen, Amal Abdi, Linda Broer, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 6, 2024
International Society on Thrombosis and Haemostasis Clinical Practice Guideline for Treatment of Congenital Haemophilia-A Critical AppraisalManuela Albisetti, Jesús Ardila, Jan Astermark, et al.Pageof 11