Mutations of optineurin in amyotrophic lateral sclerosis von Kawakami, Hideshi, Kawata, Akihiro, Maruyama, Hirofumi, Nodera, Hiroyuki, Komure, Osamu, Abe, Koji, Ito, Hidefumi, Hirano, Asao, Kinoshita, Yoshimi, Kato, Hidemasa, Hagiwara, Koichi, Watanabe, Yasuhito, Ogasawara, Kazumasa, Hirai, Takeshi, Takumi, Toru, Kato, Takeo, Morimoto, Nobutoshi, Morino, Hiroyuki, Kamada, Masaki, Kobatake, Keitaro, Suzuki, Naoki, Aoki, Masashi, Izumi, Yuishin, Matsuura, Shinya, Kaji, Ryuji, Suzuki, Hidenori, Kusaka, Hirofumi

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DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion i... von Terasaki, Akane, Nakamura, Masayuki, Urata, Yuka, Hiwatashi, Hanae, Yokoyama, Izumi, Yasuda, Takeshi, Onuma, Teiichi, Wada, Kazumaru, Kaneko, Sunao, Kan, Rumiko, Niwa, Shin-Ichi, Hashimoto, Ohiko, Komure, Osamu, Goto, Yu-Ichi, Yamagishi, Yuko, Nakano, Misa, Furusawa, Yoshihiko, Sano, Akira

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Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA rep... von Terasaki, Akane, Nakamura, Masayuki, Urata, Yuka, Hiwatashi, Hanae, Yokoyama, Izumi, Yasuda, Takeshi, Onuma, Teiichi, Wada, Kazumaru, Kaneko, Sunao, Kan, Rumiko, Niwa, Shin-Ichi, Hashimoto, Ohiko, Komure, Osamu, Goto, Yu-Ichi, Yamagishi, Yuko, Nakano, Misa, Furusawa, Yoshihiko, Sano, Akira

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Brain-derived growth factor and nerve growth factor concentrations are decreased in the substantia nigra in Parkinson's disease von Mogi, Makio, Togari, Akifumi, Kondo, Tomoyoshi, Mizuno, Yoshikuni, Komure, Osamu, Kuno, Sadako, Ichinose, Hiroshi, Nagatsu, Toshiharu

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Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations von Ayaki, Takashi, Ito, Hidefumi, Komure, Osamu, Kamada, Masaki, Nakamura, Masataka, Wate, Reika, Kusaka, Hirofumi, Yamaguchi, Yuko, Li, Fangzhou, Kawakami, Hideshi, Urushitani, Makoto, Takahashi, Ryosuke

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C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8 von Kume, Kodai, Morino, Hiroyuki, Komure, Osamu, Matsuda, Yukiko, Ohsawa, Ryosuke, Kurashige, Takashi, Kanaya, Yuhei, Tada, Yui, Kawakami, Hideshi

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Triggering of neuronal cell death by accumulation of activated SEK1 on nuclear polyglutamine aggregations in PML bodies von Yasuda, Shingo, Inoue, Kiyoshi, Hirabayashi, Miho, Higashiyama, Hiroyuki, Yamamoto, Yukio, Fuyuhiro, Haruko, Komure, Osamu, Tanaka, Fumiaki, Sobue, Gen, Tsuchiya, Kuniaki, Hamada, Koji, Sasaki, Hidenao, Takeda, Kohsuke, Ichijo, Hidenori, Kakizuka, Akira

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Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation von Ito, Hidefumi, Nakamura, Masataka, Komure, Osamu, Ayaki, Takashi, Wate, Reika, Maruyama, Hirofumi, Nakamura, Yoshimi, Fujita, Kengo, Kaneko, Satoshi, Okamoto, Yoko, Ihara, Masafumi, Konishi, Tetsuro, Ogasawara, Kazumasa, Hirano, Asao, Kusaka, Hirofumi, Kaji, Ryuji, Takahashi, Ryosuke, Kawakami, Hideshi

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Expression of Kruppel-like factor 5 gene in human brain and association of the gene with the susceptibility to schizophrenia von Yanagi, Masaya, Hashimoto, Takeshi, Kitamura, Noboru, Fukutake, Masaaki, Komure, Osamu, Nishiguchi, Naoki, Kawamata, Toshio, Maeda, Kiyoshi, Shirakawa, Osamu

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Phenotypic heterogeneity within a new family with the MAPT p301s mutation von Yasuda, Minoru, Nakamura, Yoshitsugu, Kawamata, Toshio, Kaneyuki, Hiroshi, Maeda, Kiyoshi, Komure, Osamu

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SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6 von Izumi, Yuishin, Maruyama, Hirofumi, Oda, Masaya, Morino, Hiroyuki, Okada, Takayuki, Ito, Hidefumi, Sasaki, Iwao, Tanaka, Hiroyasu, Komure, Osamu, Udaka, Fukashi, Nakamura, Shigenobu, Kawakami, Hideshi

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Anticipation in hereditary dentatorubral-pallidoluysian atrophy von SANO, A, YAMAUCHI, N, KAKIMOTO, Y, KOMURE, O, KAWAI, J, HAZAMA, F, KUZUME, K, SANO, N, KONDO, I

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Contribution of the interleukin-1β gene polymorphism in multiple system atrophy von Nishimura, Masataka, Kawakami, Hideshi, Komure, Osamu, Maruyama, Hirofumi, Morino, Hiroyuki, Izumi, Yuishin, Nakamura, Shigenobu, Kaji, Ryuji, Kuno, Sadako

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Molecular Features of the CAG Repeats of Spinocerebellar Ataxia 6 (SCA6) von Matsuyama, Zenjiro, Kawakami, Hideshi, Maruyama, Hirofumi, Izumi, Yuishin, Komure, Osamu, Udaka, Fukashi, Kameyama, Masakuni, Nishio, Takeshi, Kuroda, Yasuo, Nishimura, Masataka, Nakamura, Shigenobu

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Transgenic Mice Harboring a Full-Length Human Mutant DRPLA Gene Exhibit Age-Dependent Intergenerational and Somatic Instabilities of CAG repeats Comparable with Those in DRPLA pati... von Sato, Toshiya, Oyake, Mutsuo, Nakamura, Kenji, Nakao, Kazuki, Fukusima, Yoshimitsu, Onodera, Osamu, Igarashi, Shuichi, Takano, Hiroki, Kikugawa, Koki, Ishida, Yoshinori, Shimohata, Takayoshi, Koide, Reiji, Ikeuchi, Takeshi, Tanaka, Hajime, Futamura, Naonobu, Matsumura, Ryusuke, Takayanagi, Tetsuya, Tanaka, Fumiaki, Sobue, Gen, Komure, Osamu, Takahashi, Mie, Sano, Akira, Ichikawa, Yaeko, Goto, Jun, Kanazawa, Ichiro, Katsuki, Motoya, Tsuji, Shoji

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Present Conditions and Problems in the Departments of Neurology in the National Hospital Organization von NOZAKI, Sonoko, ANDO, Noriaki, KOMURE, Osamu, SAITO, Yuko, FUNAKAWA, Itaru, MATSUMURA, Tsuyoshi, YUASA, Tatsuhiko

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Phenotypic heterogeneity within a new family with the MAPT P501S mutation von YASUDA, Minoru, NAKAMURA, Yoshitsugu, KAWAMATA, Toshio, KANEYUKI, Hiroshi, MAEDA, Kiyoshi, KOMURE, Osamu

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The Effect of tau genotype on clinical features in FTDP-17 von Baba, Yasuhiko, Tsuboi, Yoshio, Baker, Matthew C., Uitti, Ryan J., Hutton, Michael L., Dickson, Dennis W., Farrer, Matthew, Putzke, John D., Woodruff, Bryan K., Ghetti, Bernardino, Murrell, Jill R., Boeve, Bradley F., Petersen, Ronald C., Verpillat, Patrice, Brice, Alexis, Delisle, Marie-Bernadette, Rascol, Oliver, Arima, Kunimasa, Dysken, Maurice W., Yasuda, Minoru, Kobayashi, Tomonori, Sunohara, Nobuhiko, Komure, Osamu, Kuno, Sadako, Sperfeld, Anne D., Stoppe, Gabriela, Kohlhase, Jürgen, Pickering-Brown, Stuart, Neary, David, Bugiani, Orso, Wszolek, Zbigniew K.

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A STUDY ON THE SAFETY AND COMPLICATIONS OF PERCUTANEOUS ENDOSCOPIC GASTROSTOMY (PEG) FOR CHRONIC NEUROLOGICAL AND MUSCULAR DISEASE von NOZAKI, Sonoko, ANDO, Noriaki, KOMURE, Osamu, SAITO, Yuko, FUNAKAWA, Itaru

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A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease von Morino, Hiroyuki, Kawarai, Toshitaka, Izumi, Yuishin, Kazuta, Toshinari, Oda, Masaya, Komure, Osamu, Udaka, Fukashi, Kameyama, Masakuni, Nakamura, Shigenobu, Kawakami, Hideshi

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