Allard, P. N., Tagliaferri, L., Weru, V., Cario, H., Lobitz, S., Grosse, R., . . . Kunz, J. (2024). 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. European journal of haematology, 113(4), . https://doi.org/10.1111/ejh.14259
Chicago-Zitierstil (17. Ausg.)Allard, Pierre Nicolas, et al. "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." European Journal of Haematology 113, no. 4 (2024). https://doi.org/10.1111/ejh.14259.
MLA-Zitierstil (9. Ausg.)Allard, Pierre Nicolas, et al. "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." European Journal of Haematology, vol. 113, no. 4, 2024, https://doi.org/10.1111/ejh.14259.