宮本亮介

Miyamoto Ryosuke

所属機関・部署：
職名：助教

研究分野 (1件)：神経科学一般

論文 (62件)：

Kodai Kume, Hiroyuki Morino, Ryosuke Miyamoto, Yukiko Matsuda, Ryosuke Ohsawa, Yuhei Kanaya, Yui Tada, Takashi Kurashige, Hideshi Kawakami. Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report. BMC medical genetics. 2020. 21. 1. 68-68
Yukiko Matsuda, Hiroyuki Morino, Ryosuke Miyamoto, Takashi Kurashige, Kodai Kume, Noriyoshi Mizuno, Yuhei Kanaya, Yui Tada, Ryosuke Ohsawa, Kazunori Yokota, et al. Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia. Neurology. Genetics. 2020. 6. 1. e396
Koji Fujita, Tomoyasu Matsubara, Ryosuke Miyamoto, Hiroyuki Sumikura, Toshiaki Takeuchi, Keiko Maruyama Saladini, Toshitaka Kawarai, Hiroyuki Nodera, Fukashi Udaka, Kodai Kume, et al. Co-morbidity of progressive supranuclear palsy and amyotrophic lateral sclerosis: a clinical-pathological case report. BMC Neurology. 2019. 19. 1. 168
Kawarai T, Yamazaki H, Miyamoto R, Takamatsu N, Mori A, Osaki Y, Orlacchio A, Nodera H, Hashiguchi A, Higuchi Y, et al. PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability. Neuromuscular disorders : NMD. 2019. 29. 6. 422-426
Toshitaka Kawarai, Hiroki Yamazaki, Ryosuke Miyamoto, Naoko Takamatsu, Atsuko Mori, Yusuke Osaki, Antonio Orlacchio, Hiroyuki Nodera, Akihiro Hashiguchi, Yujiro Higuchi, et al. PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability. Neuromuscular Disorders. 2019

MISC (42件)：

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宮本 亮介