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Page 1
GATA1s induces hyperproliferation of eosinophil precursors in Down syndrome transient leukemia.
Maroz A, Stachorski L, Emmrich S, Reinhardt K, Xu J, Shao Z, Käbler S, Dertmann T, Hitzler J, Roberts I, Vyas P, Juban G, Hennig C, Hansen G, Li Z, Orkin S, Reinhardt D, Klusmann JH. Maroz A, et al. Among authors: reinhardt d, reinhardt k. Leukemia. 2014 Jun;28(6):1259-70. doi: 10.1038/leu.2013.373. Epub 2013 Dec 13. Leukemia. 2014. PMID: 24336126 Free PMC article.
Analysis of GATA1 mutations in Down syndrome transient myeloproliferative disorder and myeloid leukemia.
Alford KA, Reinhardt K, Garnett C, Norton A, Böhmer K, von Neuhoff C, Kolenova A, Marchi E, Klusmann JH, Roberts I, Hasle H, Reinhardt D, Vyas P; International Myeloid Leukemia-Down Syndrome Study Group. Alford KA, et al. Among authors: reinhardt d, reinhardt k. Blood. 2011 Aug 25;118(8):2222-38. doi: 10.1182/blood-2011-03-342774. Epub 2011 Jun 29. Blood. 2011. PMID: 21715302 Free article.
Prevalence and prognostic value of IDH1 and IDH2 mutations in childhood AML: a study of the AML-BFM and DCOG study groups.
Damm F, Thol F, Hollink I, Zimmermann M, Reinhardt K, van den Heuvel-Eibrink MM, Zwaan CM, de Haas V, Creutzig U, Klusmann JH, Krauter J, Heuser M, Ganser A, Reinhardt D, Thiede C. Damm F, et al. Among authors: reinhardt d, reinhardt k. Leukemia. 2011 Nov;25(11):1704-10. doi: 10.1038/leu.2011.142. Epub 2011 Jun 7. Leukemia. 2011. PMID: 21647152
[GATA1-mutation associated leukemia in children with trisomy 21 mosaic].
Reinhardt D, Reinhardt K, Neuhoff C, Sander A, Klusmann JH, Pekrun A, Sauerbrey A, von Stackelberg A, Rössig C, Creutzig U, Kolenova A. Reinhardt D, et al. Among authors: reinhardt k. Klin Padiatr. 2012 Apr;224(3):153-5. doi: 10.1055/s-0032-1308988. Epub 2012 Apr 18. Klin Padiatr. 2012. PMID: 22513796 German.
Low-dose cytarabine to prevent myeloid leukemia in children with Down syndrome: TMD Prevention 2007 study.
Flasinski M, Scheibke K, Zimmermann M, Creutzig U, Reinhardt K, Verwer F, de Haas V, van der Velden VHJ, von Neuhoff C, Zwaan CM, Reinhardt D, Klusmann JH. Flasinski M, et al. Among authors: reinhardt d, reinhardt k. Blood Adv. 2018 Jul 10;2(13):1532-1540. doi: 10.1182/bloodadvances.2018018945. Blood Adv. 2018. PMID: 29959152 Free PMC article. Clinical Trial.
Evaluation of dsDNA from extracellular vesicles (EVs) in pediatric AML diagnostics.
Kontopoulou E, Strachan S, Reinhardt K, Kunz F, Walter C, Walkenfort B, Jastrow H, Hasenberg M, Giebel B, von Neuhoff N, Reinhardt D, Thakur BK. Kontopoulou E, et al. Among authors: reinhardt d, reinhardt k. Ann Hematol. 2020 Mar;99(3):459-475. doi: 10.1007/s00277-019-03866-w. Epub 2020 Jan 13. Ann Hematol. 2020. PMID: 31932899 Clinical Trial.
Next-generation sequencing for minimal residual disease monitoring in acute myeloid leukemia patients with FLT3-ITD or NPM1 mutations.
Thol F, Kölking B, Damm F, Reinhardt K, Klusmann JH, Reinhardt D, von Neuhoff N, Brugman MH, Schlegelberger B, Suerbaum S, Krauter J, Ganser A, Heuser M. Thol F, et al. Among authors: reinhardt d, reinhardt k. Genes Chromosomes Cancer. 2012 Jul;51(7):689-95. doi: 10.1002/gcc.21955. Epub 2012 Mar 27. Genes Chromosomes Cancer. 2012. PMID: 22454318
DNMT3A mutations are rare in childhood acute myeloid leukemia.
Thol F, Heuser M, Damm F, Klusmann JH, Reinhardt K, Reinhardt D. Thol F, et al. Among authors: reinhardt d, reinhardt k. Haematologica. 2011 Aug;96(8):1238-40. doi: 10.3324/haematol.2011.046839. Epub 2011 Jun 17. Haematologica. 2011. PMID: 21685466 Free PMC article. No abstract available.
400 results