Researcher
Katsuya Nakamura
Shinshu Daigaku Igakubu Fuzoku Byoin
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21 papers found
All papers authored by Katsuya Nakamura
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,
Monica Banez-Coronel,
Alyssa Coyne,
Shu Guo,
Lauren A. Laboissonniere,
Yuanzheng Gu,
Saravanakumar Narayanan,
Benjamin Smith
and 7 other authors
Antibody Therapy Targeting RAN Proteins Rescues C9 ALS/FTD Phenotypes in C9orf72 Mouse Model
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,
Kimitoshi Nakamura,
Kiyoko Hattori,
Masao Ota,
Yusaku Shimizu,
Fumio Endo,
Shu-Ichi Ikeda
Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients
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,
Kunihiro Yoshida,
Akira Matsushima,
Yusaku Shimizu,
Shunichi Sato,
Hiroyuki Yahikozawa,
Shinji Ohara,
Masanobu Yazawa,
Masao Ushiyama,
Mitsuto Sato,
Hiroshi Morita,
Atsushi Inoue,
Shu-Ichi Ikeda
Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study
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,
Akinori Nakamura,
Shu-Ichi Ikeda
Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer
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,
Tsuneaki Yoshinaga,
Kazuma Kaneko,
Akinori Nakamura
A Case Report of WEBINO Syndrome with Convergence Impairment
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,
Kunihiro Yoshida,
Shu-Ichi Ikeda,
Hiroyuki Ishiura,
Yoko Fukuda,
Yuji Takahashi,
Jun Goto,
Shoji Tsuji,
Yoshihisa Takiyama
Download from www.researchgate.net
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Y. Sekijima,
K. Hattori,
K. Nagamatsu,
Y. Shimizu,
M. Yazaki,
A. Sakurai,
F. Endo,
Y. Fukushima,
S.-I. Ikeda
Download from soar-ir.repo.nii.ac.jp
,
Dai; uUSVPpym Kishida,
Aya Narita,
Kaori Adachi,
Kosaku Ohno,
Eiji Nanba,
Shu-Ichi; gmnchekh Ikeda
Download from dx.doi.org
,
Yoshiki Sekijima,
Kiyoshiro Nagamatsu,
Kunihiro Yoshida,
Shu-Ichi Ikeda
A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea
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Kunihiro Yoshida,
Tsuneaki Yoshinaga,
Minori Kodaira,
Yasuhiro Shimojima,
Yo-Ichi Takei,
Hiroshi Morita,
Katsuhiko Kayanuma,
Shu-Ichi Ikeda
Adult or late-onset triple A syndrome
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,
Yoshiki Sekijima,
Kimitoshi Nakamura,
Kiyoko Hattori,
Kiyoshiro Nagamatsu,
Yusaku Shimizu,
Takuji Yasude,
Masao Ushiyama,
Fumio Endo,
Yoshimitsu Fukushima,
Shu-Ichi Ikeda
Cerebral hemorrhage in Fabry's disease
Download from www.nature.com
,
Kunihiro Yoshida,
Hideo Makishita,
Eiko Kitamura,
Shiori Hashimoto,
Shu-Ichi Ikeda
A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2)
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,
Kunihiro Yoshida,
Daigo Miyazaki,
Hiroshi Morita,
Shu-Ichi Ikeda
Spinocerebellar ataxia type 6 (SCA6): Clinical pilot trial with gabapentin
Download from soar-ir.repo.nii.ac.jpMissing publications? Search for publications with a matching author name.