Ataxias in Brazil von Tsuji, Shoji

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Significance of hyponatremia in Kawasaki disease von Tsuji, Shoji

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The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy von Wenning, Gregor K., Stankovic, Iva, Vignatelli, Luca, Fanciulli, Alessandra, Calandra‐Buonaura, Giovanna, Seppi, Klaus, Palma, Jose‐Alberto, Meissner, Wassilios G., Krismer, Florian, Berg, Daniela, Cortelli, Pietro, Freeman, Roy, Halliday, Glenda, Höglinger, Günter, Lang, Anthony, Ling, Helen, Litvan, Irene, Low, Phillip, Miki, Yasuo, Panicker, Jalesh, Pellecchia, Maria Teresa, Quinn, Niall, Sakakibara, Ryuji, Stamelou, Maria, Tolosa, Eduardo, Tsuji, Shoji, Warner, Tom, Poewe, Werner, Kaufmann, Horacio

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Management of treatment‐resistant nocturnal enuresis von Tsuji, Shoji, Kaneko, Kazunari

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The long and winding road to the etiology of idiopathic nephrotic syndrome in children: Focusing on abnormalities in the gut microbiota von Tsuji, Shoji, Kaneko, Kazunari

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CpG demethylation enhances alpha-synuclein expression and affects the pathogenesis of Parkinson's disease von Matsumoto, Lumine, Takuma, Hiroshi, Tamaoka, Akira, Kurisaki, Hiroshi, Date, Hidetoshi, Tsuji, Shoji, Iwata, Atsushi

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Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease von Ishiura, Hiroyuki, Shibata, Shota, Yoshimura, Jun, Suzuki, Yuta, Qu, Wei, Doi, Koichiro, Almansour, M. Asem, Kikuchi, Junko Kanda, Taira, Makiko, Mitsui, Jun, Takahashi, Yuji, Ichikawa, Yaeko, Mano, Tatsuo, Iwata, Atsushi, Harigaya, Yasuo, Matsukawa, Miho Kawabe, Matsukawa, Takashi, Tanaka, Masaki, Shirota, Yuichiro, Ohtomo, Ryo, Kowa, Hisatomo, Date, Hidetoshi, Mitsue, Aki, Hatsuta, Hiroyuki, Morimoto, Satoru, Murayama, Shigeo, Shiio, Yasushi, Saito, Yuko, Mitsutake, Akihiko, Kawai, Mizuho, Sasaki, Takuya, Sugiyama, Yusuke, Hamada, Masashi, Ohtomo, Gaku, Terao, Yasuo, Nakazato, Yoshihiko, Takeda, Akitoshi, Sakiyama, Yoshio, Umeda-Kameyama, Yumi, Shinmi, Jun, Ogata, Katsuhisa, Kohno, Yutaka, Lim, Shen-Yang, Tan, Ai Huey, Shimizu, Jun, Goto, Jun, Nishino, Ichizo, Toda, Tatsushi, Morishita, Shinichi, Tsuji, Shoji

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Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP... von Ishiura, Hiroyuki, Tsuji, Shoji, Toda, Tatsushi

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Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy von Ishiura, Hiroyuki, Doi, Koichiro, Mitsui, Jun, Yoshimura, Jun, Matsukawa, Miho Kawabe, Fujiyama, Asao, Toyoshima, Yasuko, Kakita, Akiyoshi, Takahashi, Hitoshi, Suzuki, Yutaka, Sugano, Sumio, Qu, Wei, Ichikawa, Kazuki, Yurino, Hideaki, Higasa, Koichiro, Shibata, Shota, Mitsue, Aki, Tanaka, Masaki, Ichikawa, Yaeko, Takahashi, Yuji, Date, Hidetoshi, Matsukawa, Takashi, Kanda, Junko, Nakamoto, Fumiko Kusunoki, Higashihara, Mana, Abe, Koji, Koike, Ryoko, Sasagawa, Mutsuo, Kuroha, Yasuko, Hasegawa, Naoya, Kanesawa, Norio, Kondo, Takayuki, Hitomi, Takefumi, Tada, Masayoshi, Takano, Hiroki, Saito, Yutaka, Sanpei, Kazuhiro, Onodera, Osamu, Nishizawa, Masatoyo, Nakamura, Masayuki, Yasuda, Takeshi, Sakiyama, Yoshio, Otsuka, Mieko, Ueki, Akira, Kaida, Ken-ichi, Shimizu, Jun, Hanajima, Ritsuko, Hayashi, Toshihiro, Terao, Yasuo, Inomata-Terada, Satomi, Hamada, Masashi, Shirota, Yuichiro, Kubota, Akatsuki, Ugawa, Yoshikazu, Koh, Kishin, Takiyama, Yoshihisa, Ohsawa-Yoshida, Natsumi, Ishiura, Shoichi, Yamasaki, Ryo, Tamaoka, Akira, Akiyama, Hiroshi, Otsuki, Taisuke, Sano, Akira, Ikeda, Akio, Goto, Jun, Morishita, Shinichi, Tsuji, Shoji

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Profound downregulation of the RNA editing enzyme ADAR2 in ALS spinal motor neurons von Hideyama, Takuto, Yamashita, Takenari, Aizawa, Hitoshi, Tsuji, Shoji, Kakita, Akiyoshi, Takahashi, Hitoshi, Kwak, Shin

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Brainstem Encephalitis with Lesions Spreading along Neuroaxonal Fibers von Yamaguchi-Takegami, Nanaka, Takegami, Naoki, Miyagawa, Toji, Tsuji, Shoji

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Genomic aspects of sporadic neurodegenerative diseases von Mitsui, Jun, Tsuji, Shoji

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Adrenoleukodystrophy siblings with a novel ABCD1 missense variant presenting with phenotypic differences: a case report and literature review von Shibata, Yuka, Matsushima, Masaaki, Matsukawa, Takashi, Ishiura, Hiroyuki, Tsuji, Shoji, Yabe, Ichiro

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Idiopathic nephrotic syndrome in children: role of regulatory T cells and gut microbiota von Tsuji, Shoji, Akagawa, Shohei, Akagawa, Yuko, Yamaguchi, Tadashi, Kino, Jiro, Yamanouchi, Sohsaku, Kimata, Takahisa, Hashiyada, Masaki, Akane, Atsushi, Kaneko, Kazunari

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Dysbiosis in Gut Microbiota in Children Born Preterm Who Developed Autism Spectrum Disorder: A Pilot Study von Fujishiro, Sadayuki, Tsuji, Shoji, Akagawa, Shohei, Akagawa, Yuko, Yamanouchi, Sohsaku, Ishizaki, Yuko, Hashiyada, Masaki, Akane, Atsushi, Kaneko, Kazunari

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COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population von Porto, Kristine Joyce, Hirano, Makito, Mitsui, Jun, Chikada, Ayaka, Matsukawa, Takashi, Ishiura, Hiroyuki, Toda, Tatsushi, Kusunoki, Susumu, Tsuji, Shoji

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Human genetic variation database, a reference database of genetic variations in the Japanese population von Higasa, Koichiro, Miyake, Noriko, Yoshimura, Jun, Okamura, Kohji, Niihori, Tetsuya, Saitsu, Hirotomo, Doi, Koichiro, Shimizu, Masakazu, Nakabayashi, Kazuhiko, Aoki, Yoko, Tsurusaki, Yoshinori, Morishita, Shinichi, Kawaguchi, Takahisa, Migita, Osuke, Nakayama, Keiko, Nakashima, Mitsuko, Mitsui, Jun, Narahara, Maiko, Hayashi, Keiko, Funayama, Ryo, Yamaguchi, Daisuke, Ishiura, Hiroyuki, Ko, Wen-Ya, Hata, Kenichiro, Nagashima, Takeshi, Yamada, Ryo, Matsubara, Yoichi, Umezawa, Akihiro, Tsuji, Shoji, Matsumoto, Naomichi, Matsuda, Fumihiko

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Paraneoplastic Cerebellar Degeneration Leading to an Early Diagnosis of Peritoneal Serous Papillary Carcinoma von Yasuda, Tsutomu, Shimizu, Jun, Miyagawa, Toji, Tsutsumi, Yuri, Iwatsubo, Takeshi, Tsuji, Shoji

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The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force von Beaudin, Marie, Matilla-Dueñas, Antoni, Soong, Bing-Weng, Pedroso, Jose Luiz, Barsottini, Orlando G., Mitoma, Hiroshi, Tsuji, Shoji, Schmahmann, Jeremy D., Manto, Mario, Rouleau, Guy A, Klein, Christopher, Dupre, Nicolas

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Neuron-specific methylome analysis reveals epigenetic regulation and tau-related dysfunction of BRCA1 in Alzheimer’s disease von Mano, Tatsuo, Nagata, Kenichi, Nonaka, Takashi, Tarutani, Airi, Imamura, Tomohiro, Hashimoto, Tadafumi, Bannai, Taro, Koshi-Mano, Kagari, Tsuchida, Takeyuki, Ohtomo, Ryo, Takahashi-Fujigasaki, Junko, Yamashita, Satoshi, Ohyagi, Yasumasa, Yamasaki, Ryo, Tsuji, Shoji, Tamaoka, Akira, Ikeuchi, Takeshi, Saido, Takaomi C., Iwatsubo, Takeshi, Ushijima, Toshikazu, Murayama, Shigeo, Hasegawa, Masato, Iwata, Atsushi

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