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Pediatric Blood & Cancer|February 6, 2020
Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21Kentaro Yuzawa, Kiminori Terui, Tsutomu Toki, et al.Journal of Pediatric Hematology/Oncology|February 24, 2021
Association of Multiple Gene Polymorphisms Including Homozygous NUDT15 R139C With Thiopurine Intolerance During the Treatment of Acute Lymphoblastic LeukemiaKo Kudo, Tomohiko Sato, Yuka Takahashi, et al.Journal of Pediatric Hematology/Oncology|June 16, 2021
Isolated Bone Recurrence of Medulloblastoma With MYCN Amplification and TP53 Loss: A Case ReportYuka Takahashi, Ko Kudo, Kaoru Ogawa, et al.Genes, Chromosomes & Cancer|October 24, 2018
Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutationKo Kudo, Hiroo Ueno, Tomohiko Sato, et al.Blood|December 23, 2004
Transgenic expression of BACH1 transcription factor results in megakaryocytic impairmentTsutomu Toki, Fumiki Katsuoka, Rika Kanezaki, et al.Journal of Neurosurgery. Case Lessons|September 20, 2023
Spontaneous remission of skull Langerhans cell histiocytosis that had developed by repeated head injury: illustrative caseKota Ueno, Kosuke Katayama, Ai Mizukami, et al.Pediatric Blood & Cancer|December 19, 2020
Prognostic and therapeutic factors influencing the clinical outcome of metastatic Ewing sarcoma family of tumors: A retrospective report from the Japan Ewing Sarcoma Study GroupKatsutsugu Umeda, Takako Miyamura, Kenji Yamada, et al.Haematologica|March 23, 2011
Relapse of aplastic anemia in children after immunosuppressive therapy: a report from the Japan Childhood Aplastic Anemia Study GroupTakuya Kamio, Etsuro Ito, Akira Ohara, et al.Ejhaem|July 18, 2022
Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond-Blackfan anaemiaAkie Kobayashi, Ryusei Ohtaka, Tsutomu Toki, et al.Genes, Chromosomes & Cancer|July 22, 2014
Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in JapanIsamu Hanada, Kiminori Terui, Fumika Ikeda, et al.Pageof 3