Search Results - Shingo Koyama

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    Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders by Shingo Koyama, Hidenori Sato, Manabu Wada, Toru Kawanami, Mitsuru Emi, Takeo Kato

    Published 2017
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    Impact of unilateral spatial neglect with or without other cognitive impairments on independent gait recovery in stroke survivors by Yosuke Kimura, Minoru Yamada, Daisuke Ishiyama, Naohito Nishio, Yota Kunieda, Shingo Koyama, Atsushi Sato, Yuhei Otobe, Shunsuke Ohji, Mizue Suzuki, Hideyuki Ogawa, Daisuke Ito, Takeo Ichikawa, Koji Hamanaka, Naoki Tanaka, Yasushi Muroh

    Published 2018
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