Bilaketaren emaitzak - Shingo Koyama

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 nork Shingo Koyama, Hidenori Sato, Manabu Wada, Toru Kawanami, Mitsuru Emi, Takeo Kato

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Impact of unilateral spatial neglect with or without other cognitive impairments on independent gait recovery in stroke survivors nork 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

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