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Blood|November 18, 2005
KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study GroupAkira Shimada, Tomohiko Taki, Ken Tabuchi, et al.
International Journal of Hematology|November 30, 2014
Outcome of pediatric acute lymphoblastic leukemia with very late relapse: a retrospective analysis by the Tokyo Children's Cancer Study Group (TCCSG)Motohiro Kato, Atsushi Manabe, Akiko M Saito, et al.
Pediatric Blood & Cancer|September 1, 2007
Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study GroupAkira Shimada, Tomohiko Taki, Ken Tabuchi, et al.
Blood|July 20, 2002
Risk factors for evolution of acquired aplastic anemia into myelodysplastic syndrome and acute myeloid leukemia after immunosuppressive therapy in childrenSeiji Kojima, Akira Ohara, Masahiro Tsuchida, et al.
British Journal of Haematology|March 5, 2014
Clinical characteristics of 15 children with juvenile myelomonocytic leukaemia who developed blast crisis: MDS Committee of Japanese Society of Paediatric Haematology/OncologyYuko Honda, Masahiro Tsuchida, Yuji Zaike, et al.
Cureus|September 10, 2025
The Pretreatment Neutrophil-to-Eosinophil Ratio Can Predict Immune-Related Adverse Events and Outcomes in Patients With Advanced Urothelial Carcinoma Treated With Immune Checkpoint InhibitorsKeita Kobayashi, Shigeru Sakano, Hiroaki Matsumoto, et al.
Pediatric Blood & Cancer|June 6, 2009
Treatment of children with refractory anemia: the Japanese Childhood MDS Study Group trial (MDS99)Daisuke Hasegawa, Atsushi Manabe, Hiroshi Yagasaki, et al.
Blood|September 25, 2003
FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidyTakeshi Taketani, Tomohiko Taki, Kanji Sugita, et al.
International Journal of Hematology|December 7, 2007
Acute myeloid leukemia with multilineage dysplasia in childrenSouichi Adachi, Atsushi Manabe, Masue Imaizumi, et al.
Genes, Chromosomes & Cancer|July 23, 2003
AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignanciesTakeshi Taketani, Tomohiko Taki, Junko Takita, et al.
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