The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β-thalassaemia and no or low HbA expression - Allard, Pierre Nicolas; Tagliaferri, Laura; Weru, Vivienn; Cario, Holger; Lobitz, Stephan; Grosse, Regine; Bleeke, Matthias; Oevermann, Lena; Hakimeh, Dani; Jarisch, Andrea; Kopp-Schneider, Annette; Kulozik, Andreas; et al. (European journal of haematology, 2024)
Veröffentlicht: 30 June 2024