Inhibitor incidence with recombinant vs. plasma-derived FVIII in previously untreated patients with severe hemophilia A: homogeneous results from four published observational studies
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2008.02852.x/fullpdf
Reference12 articles.
1. Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A;Goudemand;Blood,2006
2. Recombinant vs. plasma-derived products, especially those with intact VWF, regarding inhibitor development;Escuriola-Ettingshausen;Haemophilia,2006
3. Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A;Chalmers;Haemophilia,2007
4. Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study;Gouw;Blood,2007
5. Associations between type of product and inhibitors in previously untreated patients (PUPs) with severe hemophilia: switches and particular products can disturb analysis;Calvez;Blood,2007
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1. Impact of the Survey of Inhibitors in Plasma‐Product Exposed Toddlers (SIPPET) study and its post hoc analyses on clinical practice in the United States: A survey of Haemophilia and Thrombosis Research Society members;Haemophilia;2019-07-02
2. Over two decades of orthopaedic surgery in patients with inhibitors-Quantifying the complication of bleeding;Haemophilia;2018-12-03
3. Biochemical characterization and immunogenicity of Neureight, a recombinant full-length factor VIII produced by fed-batch process in disposable bioreactors;Cellular Immunology;2018-09
4. A close insight to factor VIII inhibitor in the congenital hemophilia A;Expert Review of Hematology;2016-08-16
5. Key insights to understand the immunogenicity of FVIII products;Thrombosis and Haemostasis;2016
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