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High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors.
Shirai R, Osumi T, Terashima K, Kiyotani C, Uchiyama M, Tsujimoto S, Yoshida M, Yoshida K, Uchiyama T, Tomizawa D, Shioda Y, Sekiguchi M, Watanabe K, Keino D, Ueno-Yokohata H, Ohki K, Takita J, Ito S, Deguchi T, Kiyokawa N, Ogiwara H, Hishiki T, Ogawa S, Okita H, Matsumoto K, Yoshioka T, Kato M. Shirai R, et al. Among authors: matsumoto k. Eur J Hum Genet. 2020 Aug;28(8):1124-1128. doi: 10.1038/s41431-020-0614-z. Epub 2020 Mar 26. Eur J Hum Genet. 2020. PMID: 32218533 Free PMC article.
TKI dasatinib monotherapy for a patient with Ph-like ALL bearing ATF7IP/PDGFRB translocation.
Kobayashi K, Miyagawa N, Mitsui K, Matsuoka M, Kojima Y, Takahashi H, Ootsubo K, Nagai J, Ueno H, Ishibashi T, Sultana S, Okada Y, Akimoto S, Okita H, Matsumoto K, Goto H, Kiyokawa N, Ohara A. Kobayashi K, et al. Among authors: matsumoto k. Pediatr Blood Cancer. 2015 Jun;62(6):1058-60. doi: 10.1002/pbc.25327. Epub 2014 Nov 14. Pediatr Blood Cancer. 2015. PMID: 25400122
A novel recurrent EP300-ZNF384 gene fusion in B-cell precursor acute lymphoblastic leukemia.
Gocho Y, Kiyokawa N, Ichikawa H, Nakabayashi K, Osumi T, Ishibashi T, Ueno H, Terada K, Oboki K, Sakamoto H, Shioda Y, Imai M, Noguchi Y, Arakawa Y, Kojima Y, Toyama D, Hata K, Yoshida T, Matsumoto K, Kato M, Fukushima T, Koh K, Manabe A, Ohara A; Tokyo Children’s Cancer Study Group. Gocho Y, et al. Among authors: matsumoto k. Leukemia. 2015 Dec;29(12):2445-8. doi: 10.1038/leu.2015.111. Epub 2015 May 6. Leukemia. 2015. PMID: 25943178 No abstract available.
Anal Canal Carcinoma in a Child With Disorders of Sex Development.
Watanabe T, Horikawa R, Masaki H, Yoshioka T, Matsumoto K, Kanamori Y. Watanabe T, et al. Among authors: matsumoto k. Pediatr Blood Cancer. 2016 Jul;63(7):1293-5. doi: 10.1002/pbc.25988. Epub 2016 Apr 1. Pediatr Blood Cancer. 2016. PMID: 27037640
Pediatric Thromboembolism in Japan.
Tetsuhara K, Ishiguro A, Michihata N, Sensaki S, Nakadate H, Kimura Y, Tomizawa D, Matsumoto K. Tetsuhara K, et al. Among authors: matsumoto k. Indian J Pediatr. 2016 Oct;83(10):1077-81. doi: 10.1007/s12098-016-2094-2. Epub 2016 Apr 7. Indian J Pediatr. 2016. PMID: 27053184
BRAF V600 mutations in Langerhans cell histiocytosis with a simple and unique assay.
Tatsuno M, Shioda Y, Iwafuchi H, Yamazaki S, Iijima K, Takahashi C, Ono H, Uchida K, Okamura O, Matubayashi M, Okuyama T, Matsumoto K, Yoshioka T, Nakazawa A. Tatsuno M, et al. Among authors: matsumoto k. Diagn Pathol. 2016 Apr 19;11:39. doi: 10.1186/s13000-016-0489-z. Diagn Pathol. 2016. PMID: 27094161 Free PMC article.
Somatic MECOM mosaicism in a patient with congenital bone marrow failure without a radial abnormality.
Osumi T, Tsujimoto SI, Nakabayashi K, Taniguchi M, Shirai R, Yoshida M, Uchiyama T, Nagasawa J, Goyama S, Yoshioka T, Tomizawa D, Kurokawa M, Matsubara Y, Kiyokawa N, Matsumoto K, Hata K, Kato M. Osumi T, et al. Among authors: matsumoto k. Pediatr Blood Cancer. 2018 Jun;65(6):e26959. doi: 10.1002/pbc.26959. Epub 2018 Jan 22. Pediatr Blood Cancer. 2018. PMID: 29356389 No abstract available.
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