View in EDS HTML Full Text PDF Full Text

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

Saved in:
Bibliographic Details
Title: 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
Authors: Allard, Pierre1 (AUTHOR), Tagliaferri, Laura1,2 (AUTHOR), Weru, Vivienn3 (AUTHOR), Cario, Holger2,4 (AUTHOR), Lobitz, Stephan2,5 (AUTHOR), Grosse, Regine2 (AUTHOR), Bleeke, Matthias2,6 (AUTHOR), Oevermann, Lena2,7 (AUTHOR), Hakimeh, Dani2,7 (AUTHOR), Jarisch, Andrea2,8 (AUTHOR), Kopp‐Schneider, Annette3 (AUTHOR), Kulozik, Andreas E.1,2 (AUTHOR), Kunz, Joachim B.1,2 (AUTHOR) joachim.kunz@med.uni-heidelberg.de, Lassay, Lisa (AUTHOR), Kontny, Udo (AUTHOR), Frühwald, Michael (AUTHOR), Westphal, Silke (AUTHOR), Holzapfel, Johannes (AUTHOR), Schulte, Johannes (AUTHOR), Eckert, Maike (AUTHOR)
Source: European Journal of Haematology. Oct2024, Vol. 113 Issue 4, p501-509. 9p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
Description
ISSN:09024441
DOI:10.1111/ejh.14259