Validation of and proposals for refinements of the WHO 2016 classification for myelodysplastic syndromes-Reference-Cited by-同舟云学术

Validation of and proposals for refinements of the WHO 2016 classification for myelodysplastic syndromes

Published:2017-08-24 Issue:11 Volume:92 Page:E631-E634
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

van Spronsen Margot F.¹^ORCID,Westers Theresia M.¹,Rozema Hanne²,Ossenkoppele Gert J.¹,Kibbelaar Robby E.²,Hoogendoorn Mels²,van de Loosdrecht Arjan A.¹

Affiliation:

1. Department of Haematology; VU University Medical Center, Cancer Center Amsterdam; The Netherlands

2. Department of Haematology; Medical Center Leeuwarden; The Netherlands

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.24867/fullpdf

Reference17 articles.

1. The genetic basis of phenotypic heterogeneity in myelodysplastic syndromes;Raza;Nat Rev Cancer.,2012

2. The multifaceted nature of myelodysplastic syndromes: clinical, molecular, and biological prognostic features;Greenberg;J Natl Compr Canc Netw.,2013

3. Clinical and biological implications of driver mutations in myelodysplastic syndromes;Papaemmanuil;Blood.,2013

4. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia;Arber;Blood.,2016

5. New proposals of the WHO working group (2016) for the diagnosis of myelodysplastic syndromes (MDS): characteristics of refined MDS types;Strupp;Leuk Res.,2017

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1. Abnormal platelet immunophenotypes and percentage of giant platelets in myelodysplastic syndrome: A pilot study;PLOS ONE;2022-11-21

2. Comparison of the revised 4th (2016) and 5th (2022) editions of the World Health Organization classification of myelodysplastic neoplasms;Leukemia;2022-10-12

3. Long Non-coding RNAs in Myeloid Malignancies;Frontiers in Oncology;2019-10-18

4. Mutations and prognosis in myelodysplastic syndromes: karyotype-adjusted analysis of targeted sequencing in 300 consecutive cases and development of a genetic risk model;American Journal of Hematology;2018-02-24