Pediatric erythroblastic transformation of <i>JAK</i>2‐mutated prefibrotic primary myelofibrosis with concurrent <i>PHF6</i> mutations-Reference-Cited by-同舟云学术

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Pediatric erythroblastic transformation of JAK2‐mutated prefibrotic primary myelofibrosis with concurrent PHF6 mutations

Published:2023-06-19 Issue:10 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Oshiro Tokiko¹,Hamada Satoru¹^ORCID,Kiyuna Sinobu¹,Sakiyama Hideki¹,Hyakuna Nobuyuki²,Tamaki Tomoko³,Muramatsu Hideki⁴,Nakanishi Koichi⁵

Affiliation:

1. Department of Pediatrics University of Ryukyus Hospital Nakagami‐gun Japan

2. Okinawa Prefectural Red Cross Blood Center Naha Japan

3. Department of Pathology and Oncology, Graduate School of Medicine University of Ryukyus Nakagami‐gun Japan

4. Department of Pediatrics, Graduate School of Medicine University of Nagoya Nagoya Japan

5. Department of Pediatrics, Graduate School of Medicine University of The Ryukyus Nakagami‐gun Japan

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30508

Reference11 articles.

1. Primary myelofibrosis: 2017 update on diagnosis, risk‐stratification, and management

2. Clinical and molecular features of patients with prefibrotic primary myelofibrosis previously diagnosed as having essential thrombocythemia in Japan

3. Clinical, histopathologic, and genetic features of pediatric primary myelofibrosis-An entity different from adults

4. The evolving genomic landscape of myeloproliferative neoplasms

5. Leukemia secondary to myeloproliferative neoplasms

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