Haemate P/Humate-P: a systematic review-Reference-Cited by-同舟云学术

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Haemate P/Humate-P: a systematic review

Published:2009-11 Issue: Volume:124 Page:S11-S14
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Berntorp Erik

Publisher

Elsevier BV

Subject

Hematology

Reference21 articles.

1. Haemate® P von Willebrand factor/factor VIII concentrate: 25 years of clinical experience;Schramm;Haemophilia,2008

2. A systematic overview of the first pasteurised VWF/FVIII medicinal product, Haemate® P/Humate-P®: history and clinical performance;Berntorp;Eur J Haematol,2008

3. Comparative analysis and classification of von Willebrand factor/factor VIII concentrates: impact on treatment of patients with von Willebrand disease;Budde;Semin Thromb Haemost,2006

4. Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrate (Humate-P);Gill;Haemophilia,2003

5. Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrate (Humate-P®);Thompson;Haemophilia,2004

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Acquired von Willebrand syndrome during extracorporeal membrane oxygenation support: a comprehensive review of current evidence: communication from the ISTH SSC on perioperative and critical care thrombosis and hemostasis;Journal of Thrombosis and Haemostasis;2024-09

2. Optimal design of infusion tests for the identification of physiological models of acquired von Willebrand syndrome;Chemical Engineering Science;2024-03

3. An open‐label, multi‐centre, post‐marketing study to assess the efficacy and safety of a plasma‐derived VWF/FVIII concentrate in patients with von Willebrand disease;Haemophilia;2023-11-29

4. Acute intraoperative subgaleal hematoma associated with vitreoretinal surgery in a patient with Ehlers-Danlos Syndrome Type VI;Ophthalmic Genetics;2022-11-28

5. Towards novel treatment options in von Willebrand disease;Haemophilia;2022-05

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