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International Journal of Hematology|February 25, 2018
Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasiaMotoshi Sonoda, Masataka Ishimura, Yuko Ichimiya, et al.Pediatric Blood & Cancer|December 27, 2023
Transient erythroblastopenia due to a GATA1 variant in an infant femaleMotoi Yamashita, Takahiro Tomoda, Ami Mizuo, et al.European Journal of Pediatrics|October 1, 2014
Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal childrenRintaro Ono, Daisuke Hasegawa, Shinsuke Hirabayashi, et al.International Journal of Hematology|July 4, 2018
Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasiaMotoshi Sonoda, Masataka Ishimura, Yuko Ichimiya, et al.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.Clinical Journal of Gastroenterology|July 10, 2020
Outcome of colorectal cancer in Diamond-Blackfan syndrome with a ribosomal protein S19 mutationKazuya Kimura, Kazuhiro Shimazu, 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.Pediatric Hematology and Oncology|February 24, 2021
Usefulness of functional splicing analysis to confirm precise disease pathogenesis in Diamond-Blackfan anemia caused by intronic variants in RPS19Satoru Takafuji, Takeshi Mori, Noriyuki Nishimura, 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.Pageof 7