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Thrombosis and Haemostasis|February 12, 1999
Inhibitors in German hemophilia A patients treated with a double virus inactivated factor VIII concentrate bind to the C2 domain of FVIII light chainR Laub, M Di Giambattista, P Fondu, et al.
British Journal of Haematology|August 1, 1995
Transplanted sickle-cell disease patients with autologous bone marrow recovery after graft failure develop increased levels of fetal haemoglobin which corrects disease severityA Ferster, F Corazza, F Vertongen, et al.
Revue Medicale De Bruxelles|August 8, 2001
[Prevention of hemoglobinopathies in Brussels: a necessity?]B Gulbis, F Cotton, V Hansen, et al.
Thrombosis and Haemostasis|August 1, 1995
Pharmacokinetics and tolerability of factor XIII concentrates prepared from human placenta or plasma: a crossover randomised studyH H Brackmann, R Egbring, A Ferster, et al.
British Journal of Haematology|August 1, 1994
Dose of desferrioxamine and evolution of HIV-1 infection in thalassaemic patientsD G Costagliola, M de Montalembert, J J Lefrère, et al.
Acta Clinica Belgica|January 1, 1997
Comparative study of antiphospholipid antibody detection in eleven Belgian laboratoriesP Capel, J Arnout, P Cauchie, et al.
Blood|May 23, 2001
Five years of experience with hydroxyurea in children and young adults with sickle cell diseaseA Ferster, P Tahriri, C Vermylen, et al.
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