Prevalence of IgG antibodies to human parvovirus B19 in haemophilia children treated with recombinant factor (F)VIII only or with at least one plasma-derived FVIII or FIX concentrate: results from the French haemophilia cohort

Author:

Gaboulaud Valérie,Parquet Armelle,Tahiri Cedric,Claeyssens Ségolène,Potard Valérie,Faradji Albert,Peynet Jocelyne,Costagliola Dominique,

Publisher

Wiley

Subject

Hematology

Reference33 articles.

1. A multicenter pharmacosurveillance study for the evaluation of the efficacy and safety of recombinant factor VIII in the treatment of patients with hemophilia A;Aygören-Pürsün;Thrombosis and Haemostasis,1997

2. Human parvovirus B19 infection in haemophiliacs first infused with two high-purity, virally atenuated factor VIII concentrates;Azzi;American Journal of Hematology,1992

3. Human parvovirus infection in haemophiliacs first infused with treated clotting factor concentrates;Bartolomei Corsi;Journal of Medical Virology,1988

4. A multicenter study of recombinant factor VIII (Recombinate): safety, efficacy, and inhibitor risk in previously untreated patients with hemophilia A;Bray;Blood,1994

5. Nanofiltration, a new specific virus elimination method applied to high-purity factor IX and factor XI concentrates;Burnouf-Radosevich;Vox Sanguinis,1994

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