Alpha-synuclein degradation by serine protease neurosin: implication for pathogenesis of synucleinopathies by Iwata, Atsushi, Maruyama, Mieko, Akagi, Takumi, Hashikawa, Tsutomu, Kanazawa, Ichiro, Tsuji, Shoji, Nukina, Nobuyuki

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Variability in immunohistochemistries of IgM M-proteins binding to sulfated glucuronyl paragloboside by Shiina, Meiko, Kusunoki, Susumu, Miyazaki, Tai, Kanazawa, Ichiro

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A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype-phenotype correlations by Kubota, Akatsuki, Hida, Ayumi, Ichikawa, Yaeko, Momose, Yoshio, Goto, Jun, Igeta, Yukifusa, Hashida, Hideji, Yoshida, Kunihiro, Ikeda, Syu-Ichi, Kanazawa, Ichiro, Tsuji, Shoji

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Expanded Glutamine Repeat Enhances Complex Formation of Dentatorubral-Pallidoluysian Atrophy (DRPLA) Protein in Human Brains by Yazawa, Ikuru, Hazeki, Noriko, Kanazawa, Ichiro

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Reduction of GluR2 RNA editing, a molecular change that increases calcium influx through AMPA receptors, selective in the spinal ventral gray of patients with amyotrophic lateral s... by Takuma, Hiroshi, Kwak, Shin, Yoshizawa, Toshihiro, Kanazawa, Ichiro

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Machado–Joseph disease gene products carrying different carboxyl termini by Goto, Jun, Watanabe, Masahiko, Ichikawa, Yaeko, Yee, Su-Bog, Ihara, Noriyo, Endo, Kotaro, Igarashi, Shuichi, Takiyama, Yoshihisa, Gaspar, Claudia, Maciel, Patricia, Tsuji, Shoji, Rouleau, Guy A, Kanazawa, Ichiro

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Sporadic ataxias in Japan – a population-based epidemiological study by Tsuji, Shoji, Onodera, Osamu, Goto, Jun, Nishizawa, Masatoyo

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Mechanism of short-term memory and repetition in conduction aphasia and related cognitive disorders: a neuropsychological, audiological and neuroimaging study by Sakurai, Yasuhisa, Takeuchi, Sosuke, Kojima, Emiko, Yazawa, Ikuru, Murayama, Shigeo, Kaga, Kimitaka, Momose, Toshimitsu, Nakase, Hirofumi, Sakuta, Manabu, Kanazawa, Ichiro

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CLAC: a novel Alzheimer amyloid plaque component derived from a transmembrane precursor, CLAC‐P/collagen type XXV by Hashimoto, Tadafumi, Wakabayashi, Tomoko, Watanabe, Atsushi, Kowa, Hisatomo, Hosoda, Ritsuko, Nakamura, Atsushi, Kanazawa, Ichiro, Arai, Takao, Takio, Koji, Mann, David M.A., Iwatsubo, Takeshi

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Cloning and Mapping of ZNF231, a Novel Brain-Specific Gene Encoding Neuronal Double Zinc Finger Protein Whose Expression Is Enhanced in a Neurodegenerative Disorder, Multiple Syste... by Hashida, Hideji, Goto, Jun, Zhao, Nanding, Takahashi, Nobuaki, Hirai, Momoki, Kanazawa, Ichiro, Sakaki, Yoshiyuki

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Slow and selective death of spinal motor neurons in vivo by intrathecal infusion of kainic acid: implications for AMPA receptor‐mediated excitotoxicity in ALS by Sun, Hui, Kawahara, Yukio, Ito, Kyoko, Kanazawa, Ichiro, Kwak, Shin

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“Clustering Index method”: A new technique for differentiation between neurogenic and myopathic changes using surface EMG by Uesugi, Haruo, Sonoo, Masahiro, Stålberg, Erik, Matsumoto, Kohji, Higashihara, Mana, Murashima, Hideharu, Ugawa, Yoshikazu, Nagashima, Yu, Shimizu, Teruo, Saito, Hisatoshi, Kanazawa, Ichiro

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Therapeutic Strategies in Huntington's Disease by Kanazawa, Ichiro

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Anti-GQ1b IgG antibody is associated with ataxia as well as ophthalmoplegia by Kusunoki, Susumu, Chiba, Atsuro, Kanazawa, Ichiro

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Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystro... by Chiba, A, Matsumura, K, Yamada, H, Inazu, T, Shimizu, T, Kusunoki, S, Kanazawa, I, Kobata, A, Endo, T

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Preferential activation of different I waves by transcranial magnetic stimulation with a figure-of-eight-shaped coil by SAKAI, K, UGAWA, Y, TERAO, Y, HANAJIMA, R, FURUBAYASHI, T, KANAZAWA, I

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Further evidence to support different mechanisms underlying intracortical inhibition of the motor cortex by Hanajima, Ritsuko, Furubayashi, Toshiaki, Iwata, Nobue Kobayashi, Shiio, Yasushi, Okabe, Shingo, Kanazawa, Ichiro, Ugawa, Yoshikazu

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Genetic association of CTNNA3 with late-onset Alzheimer's disease in females by Miyashita, Akinori, Arai, Hiroyuki, Asada, Takashi, Imagawa, Masaki, Matsubara, Etsuro, Shoji, Mikio, Higuchi, Susumu, Urakami, Katsuya, Kakita, Akiyoshi, Takahashi, Hitoshi, Toyabe, Shinichi, Akazawa, Kohei, Kanazawa, Ichiro, Ihara, Yasuo, Kuwano, Ryozo

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Pelizaeus-Merzbacher disease: Three novel mutations and implication for locus heterogeneity by Osaka, Hitoshi, Kawanishi, Chiaki, Inoue, Ken, Onishi, Hideki, Kobayashi, Takuya, Sugiyama, Naoya, Kosaka, Kenji, Nezu, Atsuo, Fujii, Katsunori, Sugita, Katsuo, Kodama, Kazuo, Murayama, Keiko, Murayama, Shigeo, Kanazawa, Ichiro, Kimura, Seiji

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Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1 by Ichikawa, Yaeko, Ishiura, Hiroyuki, Mitsui, Jun, Takahashi, Yuji, Kobayashi, Shunsuke, Takuma, Hiroshi, Kanazawa, Ichiro, Doi, Koichiro, Yoshimura, Jun, Morishita, Shinichi, Goto, Jun, Tsuji, Shoji

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