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Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome.
Nishimura A, Hirabayashi S, Hasegawa D, Yoshida K, Shiraishi Y, Ashiarai M, Hosoya Y, Fujiwara T, Harigae H, Miyano S, Ogawa S, Manabe A. Nishimura A, et al. Among authors: hosoya y. Pediatr Blood Cancer. 2021 Feb;68(2):e28799. doi: 10.1002/pbc.28799. Epub 2020 Nov 16. Pediatr Blood Cancer. 2021. PMID: 33200495 Free article.
[Transplantation-associated thrombotic microangiopathy confirmed by renal biopsy].
Miyamoto S, Kimura S, Hosoya Y, Hasegawa D, Ishida H, Daida A, Matsui T, Yoshimoto Y, Hirabayashi S, Fujimaru T, Kumamoto T, Mori SI, Suzuki K, Manabe A. Miyamoto S, et al. Among authors: hosoya y. Rinsho Ketsueki. 2018;59(4):389-394. doi: 10.11406/rinketsu.59.389. Rinsho Ketsueki. 2018. PMID: 29743397 Japanese.
Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma.
Kimura S, Hasegawa D, Yoshimoto Y, Seki M, Daida A, Sekiguchi M, Hirabayashi S, Hosoya Y, Kobayashi M, Miyano S, Ogawa S, Takita J, Manabe A. Kimura S, et al. Among authors: hosoya y. Oncol Lett. 2019 Mar;17(3):3323-3329. doi: 10.3892/ol.2019.9985. Epub 2019 Jan 29. Oncol Lett. 2019. PMID: 30867766 Free PMC article.
Very late relapse cases of TCF3-ZNF384-positive acute lymphoblastic leukemia.
Nishimura A, Hasegawa D, Hirabayashi S, Kanabuchi S, Yamamoto K, Aiga S, Nishitani M, Hosoya Y, Noguchi Y, Ohki K, Kiyokawa N, Mori S, Manabe A. Nishimura A, et al. Among authors: hosoya y. Pediatr Blood Cancer. 2019 Nov;66(11):e27891. doi: 10.1002/pbc.27891. Epub 2019 Jul 26. Pediatr Blood Cancer. 2019. PMID: 31347769 No abstract available.
432 results