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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CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy von Hirano, Makito, Kuwahara, Motoi, Yamagishi, Yuko, Samukawa, Makoto, Fujii, Kanako, Yamashita, Shoko, Ando, Masahiro, Oka, Nobuyuki, Nagano, Mamoru, Matsui, Taro, Takeuchi, Toshihide, Saigoh, Kazumasa, Kusunoki, Susumu, Takashima, Hiroshi, Nagai, Yoshitaka

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Memantine administration prevented chorea movement in Huntington’s disease: a case report von Saigoh, Kazumasa, Hirano, Makito, Mitsui, Yoshiyuki, Oda, Itsuki, Ikegawa, Atsuko, Samukawa, Makoto, Yoshikawa, Keisuke, Yamagishi, Yuko, Kusunoki, Susumu, Nagai, Yoshitaka

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Diagnosis of Parkinson’s disease and the level of oxidized DJ-1 protein von Yamagishi, Yuko, Saigoh, Kazumasa, Saito, Yoshiro, Ogawa, Ikuko, Mitsui, Yoshiyuki, Hamada, Yukihiro, Samukawa, Makoto, Suzuki, Hidekazu, Kuwahara, Motoi, Hirano, Makito, Noguchi, Noriko, Kusunoki, Susumu

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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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Varied antibody reactivities and clinical relevance in anti-GQ1b antibody–related diseases von Yoshikawa, Keisuke, Kuwahara, Motoi, Morikawa, Miyuki, Fukumoto, Yuta, Yamana, Masaki, Yamagishi, Yuko, Kusunoki, Susumu

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The novel de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Japanese case von Yoshikawa, Keisuke, Kuwahara, Motoi, Saigoh, Kazumasa, Ishiura, Hiroyuki, Yamagishi, Yuko, Hamano, Yuta, Samukawa, Makoto, Suzuki, Hidekazu, Hirano, Makito, Mitsui, Yoshiyuki, Tsuji, Shoji, Kusunoki, Susumu

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Trimacrocyclic arylamine and its polycationic states von Ito, Akihiro, Yamagishi, Yuko, Fukui, Koji, Inoue, Syuuzi, Hirao, Yasukazu, Furukawa, Ko, Kato, Tatsuhisa, Tanaka, Kazuyoshi

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The prognosis and prognostic factor of Guillain-Barré Syndrome von Yamagishi, Yuko, Kusunoki, Susumu

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The prognosis and prognostic factor of Guillain-Barré Syndrome von Yamagishi, Yuko, Kusunoki, Susumu

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Takotsubo cardiomyopathy in Guillain–Barré syndrome von Terayama, Atsushi, Kuwahara, Motoi, Yoshikawa, Keisuke, Yamagishi, Yuko, Samukawa, Makoto, Yamashita, Shoko, Onishi, Kyohei, Nagano, Tomoya, Tatsumi, Chikao, Ishii, Junko, Kawamoto, Michi, Tokashiki, Takashi, Deguchi, Shoko, Deguchi, Kentaro, Ishida, Atsushi, Baba, Yasuhiko, Yamaguchi, Shigeki, Kusunoki, Susumu, Nagai, Yoshitaka

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Charcot–Marie–Tooth disease with a mutation in FBLN5 accompanying with the small vasculitis and widespread onion-bulb formations von Yamagishi, Yuko, Samukawa, Makoto, Kuwahara, Motoi, Takada, Kazuo, Saigoh, Kazumasa, Mitsui, Yoshiyuki, Oka, Nobuyuki, Hashiguchi, Akihiro, Takashima, Hiroshi, Kusunoki, Susumu

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Predicting Outcome in Guillain-Barré Syndrome: International Validation of the Modified Erasmus GBS Outcome Score

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Markers for Guillain‐Barré syndrome with poor prognosis: a multi‐center study von Yamagishi, Yuko, Suzuki, Hidekazu, Sonoo, Masahiro, Kuwabara, Satoshi, Yokota, Takanori, Nomura, Kyoichi, Chiba, Atsuro, Kaji, Ryuji, Kanda, Takashi, Kaida, Kenichi, Ikeda, Shu‐ichi, Mutoh, Tatsuro, Yamasaki, Ryo, Takashima, Hiroshi, Matsui, Makoto, Nishiyama, Kazutoshi, Sobue, Gen, Kusunoki, Susumu

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Time Course of Radiological Imaging and Variable Interindividual Symptoms in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Associated with p.Arg487His Mutation in the V... von Hirano, Makito, Yamagishi, Yuko, Yanagimoto, Satoshi, Saigoh, Kazumasa , Nakamura, Yusaku, Kusunoki, Susumu

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An overlap case of Fisher syndrome and pharyngeal-cervical-brachial variant of Guillain-Barré syndrome associated with urinary retention and constipation von Sakai, Toshiyuki, Kondo, Masahide, Tomimoto, Hidekazu, Yamagishi, Yuko

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ギラン・バレー症候群の予後と予後予測因子 von 山岸, 裕子, 楠, 進

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International Validation of the Erasmus Guillain–Barré Syndrome Respiratory Insufficiency Score von Doets, Alex Y, Walgaard, Christa, Lingsma, Hester F, Islam, Badrul, Papri, Nowshin, Yamagishi, Yuko, Kusunoki, Susumu, Dimachkie, Mazen M, Waheed, Waqar, Kolb, Noah, Gorson, Kenneth C, Jacobs, Bart C

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尿閉と便秘を随伴し，Fisher症候群にpharyngeal-cervical-brachial variantがオーバーラップした1例 von 坂井, 利行, 近藤, 昌秀, 冨本, 秀和, 山岸, 裕子

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Charcot-Marie-Tooth disease with a mutation in FBLN5 accompanying with the small vasculitis and widespread onion-bulb formations von Yamagishi, Yuko, Samukawa, Makoto, Kuwahara, Motoi, Takada, Kazuo, Saigoh, Kazumasa, Mitsui, Yoshiyuki, Oka, Nobuyuki, Hashiguchi, Akihiro, Takashima, Hiroshi, Kusunoki, Susumu

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