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Haematologica|May 15, 2025
Marginal zone lymphoma with anti-factor H IgM and atypical hemolytic uremic syndrome successfully treated with odronextamabGianluigi Ardissino, Piera Angelillo, Maria Cristina Mancuso, et al.Haematologica|January 22, 2026
Thrombophilia screening in patients with autoimmune hemolytic anemia: a single-center analysisBruno Fattizzo, Maria Abbatista, Nicola Cecchi, et al.Haematologica|May 30, 2020
Kreuth V initiative: European consensus proposals for treatment of hemophilia using standard products, extended half-life coagulation factor concentrates and non-replacement therapiesFlora Peyvandi, Karin Berger, Rainer Seitz, et al.Journal of Thrombosis and Haemostasis : JTH|September 13, 2024
The management of liver disease in people with congenital bleeding disorders: guidance from European Association for Haemophilia and Allied Disorders, European Haemophilia Consortium, ISTH, and World Federation of HemophiliaVincenzo La Mura, Massimo Colombo, Graham R Foster, et al.Critical Care (London, England)|August 15, 2012
Prognostic utility and characterization of cell-free DNA in patients with severe sepsisDhruva J Dwivedi, Lisa J Toltl, Laura L Swystun, et al.Nature Medicine|February 16, 2024
Anticoagulation with osocimab in patients with kidney failure undergoing hemodialysis: a randomized phase 2 trialJeffrey I Weitz, László B Tankó, Jürgen Floege, et al.Journal of Thrombosis and Haemostasis : JTH|December 17, 2020
Establishment of a framework for assessing mortality in persons with congenital hemophilia A and its application to an adverse event reporting databaseSteven W Pipe, Rebecca Kruse-Jarres, Johnny N Mahlangu, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 19, 2012
The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndromeFrancesca Crovetto, Nicolò Borsa, Barbara Acaia, et al.Blood Advances|September 3, 2024
Liver-related aspects of valoctocogene roxaparvovec gene therapy for hemophilia A: expert guidance for clinical practiceVincenzo La Mura, Vincenzo Cardinale, Raimondo De Cristofaro, et al.Journal of Thrombosis and Haemostasis : JTH|September 7, 2025
Evaluation of different platelet-dependent von Willebrand factor activity assays to assess the in vivo inhibitory effect of caplacizumab on the von Willebrand factor-platelet interactionPaola Colpani, Luciano Baronciani, Ilaria Mancini, et al.Pageof 87