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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

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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
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  Data: 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
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Haematology%22">European Journal of Haematology</searchLink>. Oct2024, Vol. 113 Issue 4, p501-509. 9p.
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              Text: Oct2024
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