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Timing of inhibitor development in more than 1000 previously untreated patients with severe hemophilia A

Authors :
Manuel Carcao
Christoph Male
Gili Kenet
Karin Kurnik
Elena Santagostino
Rolf Ljung
Krista Fischer
H. Marijke van den Berg
Chris Königs
Hervé Chambost
PedNet Haemophilia Research Foundation
Partenaires INRAE
University Medical Center [Utrecht]
Royal Hospital for Sick Children
Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN)
Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Service de pédiatrie, d'hématologie et d'oncologie [Hôpital de La Timone - APHM]
Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)
Israeli Ministry of Health
University of Munich Medical Center
Goethe University Hospital
Medizinische Universität Wien = Medical University of Vienna
Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS)
Lund University [Lund]
Source :
Blood, Blood, American Society of Hematology, 2019, 134 (3), pp.317-320. ⟨10.1182/blood.2019000658⟩, Blood, 2019, 134 (3), pp.317-320. ⟨10.1182/blood.2019000658⟩
Publication Year :
2019
Publisher :
HAL CCSD, 2019.

Abstract

TO THE EDITOR: Inhibitory antibodies (inhibitors) against factor VIII (FVIII) develop in 25% to 35% of previously untreated patients (PUPs) with severe hemophilia A (SHA). It is the most serious complication of classic hemophilia treatment.[1][1][⇓][2]-[3][3] Most inhibitors develop during the

Details

Language :
English
ISSN :
00064971 and 15280020
Database :
OpenAIRE
Journal :
Blood, Blood, American Society of Hematology, 2019, 134 (3), pp.317-320. ⟨10.1182/blood.2019000658⟩, Blood, 2019, 134 (3), pp.317-320. ⟨10.1182/blood.2019000658⟩
Accession number :
edsair.doi.dedup.....afdb95deba4b03d8b01803d58f7d2f33