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Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing.
Kato T, Morisada N, Nagase H, Nishiyama M, Toyoshima D, Nakagawa T, Maruyama A, Fu XJ, Nozu K, Wada H, Takada S, Iijima K. Kato T, et al. Among authors: nishiyama m. Brain Dev. 2015 Oct;37(9):911-5. doi: 10.1016/j.braindev.2015.03.002. Epub 2015 Mar 27. Brain Dev. 2015. PMID: 25819767
Rituximab treatment for relapsed opsoclonus-myoclonus syndrome.
Toyoshima D, Morisada N, Takami Y, Kidokoro H, Nishiyama M, Nakagawa T, Ninchoji T, Nozu K, Takeshima Y, Takada S, Nishio H, Iijima K. Toyoshima D, et al. Among authors: nishiyama m. Brain Dev. 2016 Mar;38(3):346-9. doi: 10.1016/j.braindev.2015.09.002. Epub 2015 Sep 12. Brain Dev. 2016. PMID: 26375512
Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.
Taniguchi-Ikeda M, Takeshima Y, Lee T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K. Taniguchi-Ikeda M, et al. Among authors: nishiyama m. J Hum Genet. 2016 Apr;61(4):351-5. doi: 10.1038/jhg.2015.157. Epub 2016 Jan 7. J Hum Genet. 2016. PMID: 26740235
Short and long-term outcomes in children with suspected acute encephalopathy.
Nishiyama M, Nagase H, Tanaka T, Fujita K, Kusumoto M, Kajihara S, Yamaguchi Y, Maruyama A, Takeda H, Uetani Y, Tomioka K, Toyoshima D, Taniguchi-Ikeda M, Morioka I, Takada S, Iijima K. Nishiyama M, et al. Brain Dev. 2016 Sep;38(8):731-7. doi: 10.1016/j.braindev.2016.02.011. Epub 2016 Mar 4. Brain Dev. 2016. PMID: 26952815
A pediatric patient with interstitial pneumonia due to enterovirus D68.
Matsumoto M, Awano H, Ogi M, Tomioka K, Unzaki A, Nishiyama M, Toyoshima D, Taniguchi-Ikeda M, Ishida A, Nagase H, Morioka I, Iijima K. Matsumoto M, et al. Among authors: nishiyama m. J Infect Chemother. 2016 Oct;22(10):712-5. doi: 10.1016/j.jiac.2016.03.009. Epub 2016 Apr 22. J Infect Chemother. 2016. PMID: 27118532
1,182 results