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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Effects of l-threo-DOPS, a noradrenaline precursor, on the long-term potentiation in the rat hippocampal mossy fiber-CA3 region von Sakai, Norio, Sasa, Masashi, Ishihara, Kumatoshi, Komure, Osamu, Tanaka, Chikako, Takaori, Shuji

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Contribution of the interleukin-1b 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

Volltext

Contribution of the interleukin-1beta 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

Volltext

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

Volltext

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

Volltext