Works by Onodera, Osamu

Results: 155
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    Authors' reply.

    Published in:
    Journal of Bone & Mineral Metabolism, 2022, v. 40, n. 3, p. 537, doi. 10.1007/s00774-022-01315-9
    By:
    • Wakasugi, Minako;
    • Yokoseki, Akio;
    • Wada, Masakazu;
    • Momotsu, Takeshi;
    • Sato, Kenji;
    • Kawashima, Hiroyuki;
    • Nakamura, Kazutoshi;
    • Onodera, Osamu;
    • Narita, Ichiei
    Publication type:
    Article
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    TDP-43 transports ribosomal protein mRNA to regulate axonal local translation in neuronal axons.

    Published in:
    Acta Neuropathologica, 2020, v. 140, n. 5, p. 695, doi. 10.1007/s00401-020-02205-y
    By:
    • Nagano, Seiichi;
    • Jinno, Junki;
    • Abdelhamid, Rehab F.;
    • Jin, Yinshi;
    • Shibata, Megumi;
    • Watanabe, Shohei;
    • Hirokawa, Sachiko;
    • Nishizawa, Masatoyo;
    • Sakimura, Kenji;
    • Onodera, Osamu;
    • Okada, Hironori;
    • Okada, Takashi;
    • Saito, Yuko;
    • Takahashi-Fujigasaki, Junko;
    • Murayama, Shigeo;
    • Wakatsuki, Shuji;
    • Mochizuki, Hideki;
    • Araki, Toshiyuki
    Publication type:
    Article
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    TDP- 43 mutation in familial amyotrophic lateral sclerosis.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 4, p. 538, doi. 10.1002/ana.21392
    By:
    • Yokoseki, Akio;
    • Shiga, Atsushi;
    • Tan, Chun-Feng;
    • Tagawa, Asako;
    • Kaneko, Hiroyuki;
    • Koyama, Akihide;
    • Eguchi, Hiroto;
    • Tsujino, Akira;
    • Ikeuchi, Takeshi;
    • Kakita, Akiyoshi;
    • Okamoto, Koichi;
    • Nishizawa, Masatoyo;
    • Takahashi, Hitoshi;
    • Onodera, Osamu
    Publication type:
    Article
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    Dentatorubral-pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.

    Published in:
    Annals of Neurology, 1995, v. 37, n. 6, p. 769, doi. 10.1002/ana.410370610
    By:
    • Ikeuchi, Takeshi;
    • Koide, Reiji;
    • Tanaka, Hajime;
    • Onodera, Osamu;
    • Igarashi, Shuichi;
    • Takahashi, Hitoshi;
    • Kondo, Rui;
    • Ishikawa, Atsushi;
    • Tomoda, Akemi;
    • Miike, Teruhisa;
    • Keiko Sato;
    • Ihara, Yuetsu;
    • Hayabara, Toshiyuki;
    • Isa, Fumiko;
    • Tanabe, Hitoshi;
    • Tokiguchi, Susumu;
    • Hayashi, Masataka;
    • Shimizu, Natsue;
    • Ikuta, Fusahiro;
    • Naito, Haruhiko
    Publication type:
    Article
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    Trinucleotide repeat length and rate of progression of Huntington's disease.

    Published in:
    Annals of Neurology, 1994, v. 36, n. 4, p. 630, doi. 10.1002/ana.410360412
    By:
    • Illarioshkin, Sergei N.;
    • Igarashi, Shuichi;
    • Onodera, Osamu;
    • Markova, Elena D.;
    • Nikolskaya, Natalya N.;
    • Tanaka, Hajime;
    • Chabrashwili, Tina Z.;
    • Insarova, Nina G.;
    • Endo, Kotaro;
    • Ivanova-Smolenskaya, Irina A.;
    • Tsuji, Shoji
    Publication type:
    Article
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    Paving the Way Toward Meaningful Trials in Ataxias: An Ataxia Global Initiative Perspective.

    Published in:
    Movement Disorders, 2022, v. 37, n. 6, p. 1125, doi. 10.1002/mds.29032
    By:
    • Klockgether, Thomas;
    • Ashizawa, Tetsuo;
    • Brais, Bernard;
    • Chuang, Rosalind;
    • Durr, Alexandra;
    • Fogel, Brent;
    • Greenfield, Julie;
    • Hagen, Sue;
    • Jardim, Laura Bannach;
    • Jiang, Hong;
    • Onodera, Osamu;
    • Pedroso, José Luiz;
    • Soong, Bin‐Weng;
    • Szmulewicz, David;
    • Graessner, Holm;
    • Synofzik, Matthis
    Publication type:
    Article
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    Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations.

    Published in:
    Movement Disorders, 2021, v. 36, n. 7, p. 1634, doi. 10.1002/mds.28521
    By:
    • Seike, Naohiko;
    • Yokoseki, Akio;
    • Takeuchi, Ryoko;
    • Saito, Kento;
    • Miyahara, Hiroaki;
    • Miyashita, Akinori;
    • Ikeda, Tetsuhiko;
    • Aida, Izumi;
    • Nakajima, Takashi;
    • Kanazawa, Masato;
    • Wakabayashi, Masatoshi;
    • Toyoshima, Yasuko;
    • Takahashi, Hitoshi;
    • Matsumoto, Riki;
    • Toda, Tatsushi;
    • Onodera, Osamu;
    • Ishikawa, Atsushi;
    • Ikeuchi, Takeshi;
    • Kakita, Akiyoshi
    Publication type:
    Article
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    Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 184, doi. 10.1038/ng1001-184
    By:
    • Date, Hidetoshi;
    • Onodera, Osamu;
    • Tanaka, Hajime;
    • Iwabuchi, Kiyoshi;
    • Uekawa, Kazutoshi;
    • Igarashi, Shuichi;
    • Koike, Ryoko;
    • Hiroi, Tadashi;
    • Yuasa, Tatsuhiko;
    • Awaya, Yutaka;
    • Sakai, Tetsuo;
    • Takahashi, Tatsuya;
    • Nagatomo, Hideki;
    • Sekijima, Yoshiki;
    • Kawachi, Izumi;
    • Takiyama, Yoshihisa;
    • Nishizawa, Masatoyo;
    • Fukuhara, Nobuyoshi;
    • Saito, Kayoko
    Publication type:
    Article
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    Expanded polyglutamine stretches interact with TAF<sub>II</sub>130, interfering with CREB-dependent transcription.

    Published in:
    Nature Genetics, 2000, v. 26, n. 1, p. 29, doi. 10.1038/79139
    By:
    • Shimohata, Takayoshi;
    • Nakajima, Toshihiro;
    • Yamada, Mitsunori;
    • Uchida, Chiharu;
    • Onodera, Osamu;
    • Naruse, Satoshi;
    • Kimura, Tetsuya;
    • Koide, Reiji;
    • Nozaki, Kenkichi;
    • Sano, Yasuteru;
    • Ishiguro, Hiroshi;
    • Sakoe, Kumi;
    • Ooshima, Takayuki;
    • Sato, Aki;
    • Ikeuchi, Takeshi;
    • Oyake, Mutsuo;
    • Sato, Toshiya;
    • Aoyagi, Yasuyuki;
    • Hozumi, Isao
    Publication type:
    Article
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    Reliability study for the Japanese version of the Columbia Muscle Cramp Scale in amyotrophic lateral sclerosis.

    Published in:
    Neurology & Clinical Neuroscience, 2025, v. 13, n. 1, p. 14, doi. 10.1111/ncn3.12838
    By:
    • Sawada, Masahiro;
    • Hirayama, Takehisa;
    • Yanagihashi, Masaru;
    • Fukushima, Koji;
    • Izumi, Yuishin;
    • Naoi, Tameto;
    • Morita, Mitsuya;
    • Warita, Hitoshi;
    • Aoki, Masashi;
    • Iguchi, Yohei;
    • Katsuno, Masahisa;
    • Ogawa, Nobuhiro;
    • Urusitani, Makoto;
    • Ishihara, Tomohiko;
    • Onodera, Osamu;
    • Murakami, Yoshitaka;
    • Mitsumoto, Hiroshi;
    • Kano, Osamu
    Publication type:
    Article
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    The Japan MSA registry: A multicenter cohort study of multiple system atrophy.

    Published in:
    Neurology & Clinical Neuroscience, 2024, v. 12, n. 5, p. 271, doi. 10.1111/ncn3.12809
    By:
    • Chikada, Ayaka;
    • Orimo, Kenta;
    • Mitsui, Jun;
    • Matsukawa, Takashi;
    • Ishiura, Hiroyuki;
    • Toda, Tatsushi;
    • Mizusawa, Hidehiro;
    • Takahashi, Yuji;
    • Katsuno, Masahisa;
    • Hara, Kazuhiro;
    • Onodera, Osamu;
    • Ishihara, Tomohiko;
    • Tada, Masayoshi;
    • Kuwabara, Satoshi;
    • Sugiyama, Atsuhiko;
    • Yamanaka, Yoshitaka;
    • Takahashi, Ryosuke;
    • Sawamoto, Nobukatsu;
    • Sakato, Yusuke;
    • Ishimoto, Tomoyuki
    Publication type:
    Article
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    Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

    Published in:
    Brain: A Journal of Neurology, 2003, v. 126, n. 1, p. 134, doi. 10.1093/brain/awg012
    By:
    • Hattori, Naoki;
    • Yamamoto, Masahiko;
    • Yoshihara, Tsuyoshi;
    • Koike, Haruki;
    • Nakagawa, Masanori;
    • Yoshikawa, Hiroo;
    • Ohnishi, Akio;
    • Hayasaka, Kiyoshi;
    • Onodera, Osamu;
    • Baba, Masayuki;
    • Yasuda, Hitoshi;
    • Saito, Toyokazu;
    • Nakashima, Kenji;
    • Kira, Jun‐ichi;
    • Kaji, Ryuji;
    • Oka, Nobuyuki;
    • Sobue, Gen
    Publication type:
    Article