Author/Creator: Kawakami, Hideshi - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Kawakami, Hideshi

1. A Japanese patient with familial ALS and a p.K510M mutation in the gene for FUS (FUS) resulting in the totally locked‐in state. Issue 5 (19th May 2014)

Authors:: Mochizuki, Yoko; Kawata, Akihiro; Maruyama, Hirofumi; Homma, Taku; Watabe, Kazuhiko; Kawakami, Hideshi; Komori, Takashi; Mizutani, Toshio; Matsubara, Shiro
Journal:: Neuropathology
Issue:: Volume 34:Issue 5(2014)
Page Start:: 504
Record Type:: Journal Article
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2. A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia. Issue 1 (December 2015)

Authors:: Morino, Hiroyuki; Matsuda, Yukiko; Muguruma, Keiko; Miyamoto, Ryosuke; Ohsawa, Ryosuke; Ohtake, Toshiyuki; Otobe, Reiko; Watanabe, Masahiko; Maruyama, Hirofumi; Hashimoto, Kouichi; Kawakami, Hideshi
Journal:: Molecular brain
Issue:: Volume 8:Issue 1(2015)
Page Start:: 1
Record Type:: Journal Article
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3. Amyotrophic lateral sclerosis of long clinical course clinically presenting with progressive muscular atrophy. Issue 1 (3rd December 2018)

Authors:: Matsubara, Tomoyasu; Oda, Masaya; Takahashi, Tetsuya; Watanabe, Chigusa; Tachiyama, Yoshiro; Morino, Hiroyuki; Kawakami, Hideshi; Kaji, Ryuji; Maruyama, Hirofumi; Murayama, Shigeo; Izumi, Yuishin
Journal:: Neuropathology
Issue:: Volume 39:Issue 1(2019)
Page Start:: 47
Record Type:: Journal Article
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4. An autopsy case of familial amyotrophic lateral sclerosis with FUS R521G mutation. Issue 3 (1st June 2014)

Authors:: Mochizuki, Yoko; Kawata, Akihiro; Hashimoto, Tomoyo; Akiyama, Haruhiko; Kawakami, Hideshi; Komori, Takashi; Oyanagi, Kiyomitsu; Mizutani, Toshio; Matsubara, Shiro
Journal:: Amyotrophic lateral sclerosis and frontotemporal degeneration
Issue:: Volume 15:Issue 3/4(2014)
Page Start:: 305
Record Type:: Journal Article
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5. An autopsy case of familial amyotrophic lateral sclerosis with FUS R521G mutation. Issue 3 (June 2014)

Authors:: Mochizuki, Yoko; Kawata, Akihiro; Hashimoto, Tomoyo; Akiyama, Haruhiko; Kawakami, Hideshi; Komori, Takashi; Oyanagi, Kiyomitsu; Mizutani, Toshio; Matsubara, Shiro
Journal:: Amyotrophic lateral sclerosis and frontotemporal degeneration
Issue:: Volume 15:Issue 3/4(2014)
Page Start:: 305
Record Type:: Journal Article
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6. An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation. Issue 1 (17th June 2013)

Authors:: Nakamura, Seika; Wate, Reika; Kaneko, Satoshi; Ito, Hidefumi; Oki, Mitsuaki; Tsuge, Ayako; Nagashima, Masato; Asayama, Shinya; Fujita, Kengo; Nakamura, Masataka; Maruyama, Hirofumi; Kawakami, Hideshi; Kusaka, Hirofumi
Journal:: Neuropathology
Issue:: Volume 34:Issue 1(2014)
Page Start:: 58
Record Type:: Journal Article
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7. An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP‐43 proteinopathy. Issue 2 (7th January 2021)

Authors:: Matsubara, Tomoyasu; Izumi, Yuishin; Oda, Masaya; Takahashi, Masatoshi; Maruyama, Hirofumi; Miyamoto, Ryosuke; Watanabe, Chigusa; Tachiyama, Yoshiro; Morino, Hiroyuki; Kawakami, Hideshi; Saito, Yuko; Murayama, Shigeo
Journal:: Neuropathology
Issue:: Volume 41:Issue 2(2021)
Page Start:: 118
Record Type:: Journal Article
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8. Analysis on the Susceptibility Genes in Two Chinese Pedigrees with Familial Parkinson's Disease. (19th July 2010)

Authors:: Xu, Changshui; Xu, Jun; Zhang, Yanmin; Ma, Jianjun; Kawakami, Hideshi; Maruyama, Hirofumi; Kamada, Masaki
Other Names:: Geula Changiz Academic Editor.
Journal:: Neurology research international
Issue:: Volume 2010(2010)
Page Start:
Record Type:: Journal Article
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9. Analysis on the Susceptibility Genes in Two Chinese Pedigrees with Familial Parkinson's Disease. (19th July 2010)

Authors:: Xu, Changshui; Xu, Jun; Zhang, Yanmin; Ma, Jianjun; Kawakami, Hideshi; Maruyama, Hirofumi; Kamada, Masaki
Other Names:: Geula Changiz Academic Editor.
Journal:: Neurology research international
Issue:: Volume 2010(2010)
Page Start:
Record Type:: Journal Article
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10. Autosomal recessive Andersen–Tawil syndrome with a novel mutation L94P in Kir2.1. Issue 4 (26th August 2013)

Authors:: Takeda, Ikuko; Takahashi, Tetsuya; Ueno, Hiroki; Morino, Hiroyuki; Ochi, Kazuhide; Nakamura, Takeshi; Hosomi, Naohisa; Kawakami, Hideshi; Hashimoto, Kouichi; Matsumoto, Masayasu
Journal:: Neurology and clinical neuroscience
Issue:: Volume 1:Issue 4(2013:Jul.)
Page Start:: 131
Record Type:: Journal Article
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