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Page 1
Pregnancies and Neonatal Outcomes in Patients with Sickle Cell Disease (SCD): Still a (High-)Risk Constellation?
Proske P, Distelmaier L, Aramayo-Singelmann C, Koliastas N, Iannaccone A, Papathanasiou M, Temme C, Klump H, Lenz V, Koldehoff M, Carpinteiro A, Reinhardt HC, Köninger A, Röth A, Yamamoto R, Dührsen U, Alashkar F. Proske P, et al. Among authors: aramayo singelmann c. J Pers Med. 2021 Aug 30;11(9):870. doi: 10.3390/jpm11090870. J Pers Med. 2021. PMID: 34575647 Free PMC article.
Veno-Venous Extracorporeal Membrane Oxygenation in Adult Patients with Sickle Cell Disease and Acute Chest Syndrome: a Single-Center Experience.
Alashkar F, Herbstreit F, Carpinteiro A, Baum J, Tzalavras A, Aramayo-Singelmann C, Vance C, Lenz V, Gulbins E, Reinhardt D, Beelen DW, Dührsen U, Röth A, Koldehoff M, Liebregts T. Alashkar F, et al. Among authors: aramayo singelmann c. Hemoglobin. 2020 Mar;44(2):71-77. doi: 10.1080/03630269.2020.1745827. Epub 2020 Apr 14. Hemoglobin. 2020. PMID: 32283959
Transition in Sickle Cell Disease (SCD): A German Consensus Recommendation.
Alashkar F, Aramayo-Singelmann C, Böll J, Hoferer A, Jarisch A, Kamal H, Oevermann L, Schwarz M, Cario H. Alashkar F, et al. Among authors: aramayo singelmann c. J Pers Med. 2022 Jul 17;12(7):1156. doi: 10.3390/jpm12071156. J Pers Med. 2022. PMID: 35887653 Free PMC article.
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 P, Tagliaferri L, Weru V, Cario H, Lobitz S, Grosse R, Bleeke M, Oevermann L, Hakimeh D, Jarisch A, Kopp-Schneider A, Kulozik AE, Kunz JB; German Sickle Cell Disease Study Group; Lassay L. Allard P, et al. Eur J Haematol. 2024 Oct;113(4):501-509. doi: 10.1111/ejh.14259. Epub 2024 Jun 30. Eur J Haematol. 2024. PMID: 38946051