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Journal of Thrombosis and Haemostasis : JTH|September 27, 2019
One piece of the puzzle: Population pharmacokinetics of FVIII during perioperative Haemate P® /Humate P® treatment in von Willebrand disease patientsNico C B de Jager, Laura H Bukkems, Jessica M Heijdra, et al.Thrombosis and Haemostasis|October 2, 2018
Long-Term Outcome after Joint Bleeds in Von Willebrand Disease Compared to Haemophilia A: A Post Hoc AnalysisKarin P M van Galen, Merel Timmer, Piet de Kleijn, et al.Blood|November 8, 2019
Preterm neonates benefit from low prophylactic platelet transfusion threshold despite varying risk of bleeding or deathSusanna F Fustolo-Gunnink, Karin Fijnvandraat, David van Klaveren, et al.British Journal of Clinical Pharmacology|November 24, 2020
Dosing of factor VIII concentrate by ideal body weight is more accurate in overweight and obese haemophilia A patientsIris van Moort, Tim Preijers, Hendrika C A M Hazendonk, et al.The New England Journal of Medicine|November 3, 2018
Randomized Trial of Platelet-Transfusion Thresholds in NeonatesAnna Curley, Simon J Stanworth, Karen Willoughby, et al.Research and Practice in Thrombosis and Haemostasis|September 12, 2022
Desmopressin for bleeding in non-severe hemophilia A: Suboptimal use in a real-world settingAnne-Fleur Zwagemaker, Fabienne R Kloosterman, Michiel Coppens, et al.Research and Practice in Thrombosis and Haemostasis|December 14, 2020
ADAMTS-13 and bleeding phenotype in von Willebrand diseaseJohan Boender, Angelique Nederlof, Karina Meijer, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 15, 2018
Sports participation and physical activity in patients with von Willebrand diseaseFerdows Atiq, Eveline P Mauser-Bunschoten, Jeroen Eikenboom, et al.British Journal of Clinical Pharmacology|April 22, 2021
Validation of a perioperative population factor VIII pharmacokinetic model with a large cohort of pediatric hemophilia a patientsTim Preijers, Ri Liesner, Hendrika C A M Hazendonk, et al.Thrombosis and Haemostasis|August 25, 2012
Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand diseaseEva M de Wee, Yvonne V Sanders, Eveline P Mauser-Bunschoten, et al.Pageof 16