2016 Revision to the WHO classification of acute myeloid leukemia-Reference-Cited by-同舟云学术

2016 Revision to the WHO classification of acute myeloid leukemia

Published:2017-06-01 Issue:2 Volume:5 Page:69-71
ISSN:2224-4018
Container-title:Journal of Translational Internal Medicine
language:en
Short-container-title:

Author:

Hong Ming¹,He Guangsheng¹

Affiliation:

1. Department of Hematology , The First Affiliated Hospital of Nanjing Medical University , Jiangsu Province Hospital , Nanjing 210029 , Jiangsu Province , China

Publisher

Walter de Gruyter GmbH

Subject

Internal Medicine

Reference5 articles.

1. Groschel S, Sanders MA, Hoogenboezem R, de Wit E, Bouwman BA, Erpelinck C, et al. A single oncogenic enhancer rearrangement causes concomitant EVI1 and GATA2 deregulation in leukemia. Cell 2014;157:369-81.

2. Nacheva EP, Grace CD, Brazma D, Gancheva K, Howard-Reeves J, Rai L, et al. Does BCR/ABL1 positive acute myeloid leukemia exist? Br J Haematol 2013;161:541-50.

3. Schnittger S, Dicker F, Kern W, Wendland N, Sundermann J, Alpermann T, et al. RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis. Blood 2011;117:2348-57.

4. Mendler JH, Maharry K, Radmacher MD, Mrozek K, Becker H, Metzeler KH, et al. RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and MicroRNA expression signatures. J Clin Oncol 2012;30:3109-18.

5. Wouters BJ, Löwenberg B, Erpelinck-Verschueren CAJ, van Putten WLJ, Valk PJM, Delwel R. Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome. Blood 2009;113:3088-91.

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