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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Improving diagnostic accuracy of multiple system atrophy: a clinicopathological study von Miki, Yasuo, Foti, Sandrine C, Asi, Yasmine T, Tsushima, Eiki, Quinn, Niall, Ling, Helen, Holton, Janice L

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Neuropathology of Multiple System Atrophy, a Glioneuronal Degenerative Disease von Wakabayashi, Koichi, Miki, Yasuo, Tanji, Kunikazu, Mori, Fumiaki

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Sigma-1 receptor is involved in degradation of intranuclear inclusions in a cellular model of Huntington's disease von Miki, Yasuo, Tanji, Kunikazu, Mori, Fumiaki, Wakabayashi, Koichi

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Early presentation of urinary retention in multiple system atrophy: can the disease begin in the sacral spinal cord? von Panicker, Jalesh N., Simeoni, Sara, Miki, Yasuo, Batla, Amit, Iodice, Valeria, Holton, Janice L., Sakakibara, Ryuji, Warner, Thomas T.

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Trehalose intake and exercise upregulate a glucose transporter, GLUT8, in the brain von Narita, Hidemi, Tanji, Kunikazu, Miki, Yasuo, Mori, Fumiaki, Wakabayashi, Koichi

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Cabergoline, a long-acting dopamine agonist, attenuates L-dopa-induced dyskinesia without L-dopa sparing in a rat model of Parkinson’s disease von Nishijima, Haruo, Mori, Fumiaki, Kimura, Tamaki, Miki, Yasuo, Kinoshita, Iku, Nakamura, Takashi, Kon, Tomoya, Suzuki, Chieko, Wakabayashi, Koichi, Tomiyama, Masahiko

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Autophagy Is a Common Degradation Pathway for Bunina Bodies and TDP-43 Inclusions in Amyotrophic Lateral Sclerosis von Mori, Fumiaki, Miki, Yasuo, Kon, Tomoya, Tanji, Kunikazu, Wakabayashi, Koichi

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Is amyotrophic lateral sclerosis a prion-like disorder? A case report von Miki, Yasuo, Shibuya, Eri, Yoshizawa, Tadashi, Tomiyama, Masahiko, Wakabayashi, Koichi

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White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy von Bettencourt, Conceição, Foti, Sandrine C., Miki, Yasuo, Botia, Juan, Chatterjee, Aparajita, Warner, Thomas T., Revesz, Tamas, Lashley, Tammaryn, Balazs, Robert, Viré, Emmanuelle, Holton, Janice L.

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A mouse model of adult-onset multiple system atrophy von Tanji, Kunikazu, Miki, Yasuo, Mori, Fumiaki, Nikaido, Yoshikazu, Narita, Hidemi, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Alteration of mitochondrial protein PDHA1 in Lewy body disease and PARK14 von Miki, Yasuo, Tanji, Kunikazu, Mori, Fumiaki, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Accumulation of Nonfibrillar TDP-43 in the Rough Endoplasmic Reticulum Is the Early-Stage Pathology in Amyotrophic Lateral Sclerosis von Kon, Tomoya, Mori, Fumiaki, Tanji, Kunikazu, Miki, Yasuo, Nishijima, Haruo, Nakamura, Takashi, Kinoshita, Iku, Suzuki, Chieko, Kurotaki, Hidekachi, Tomiyama, Masahiko, Wakabayashi, Koichi

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Case report: Adult-onset neuronal intranuclear inclusion disease with an amyotrophic lateral sclerosis phenotype von Fujita, Masako, Ueno, Tatsuya, Miki, Yasuo, Arai, Akira, Kurotaki, Hidekachi, Wakabayashi, Koichi, Tomiyama, Masahiko

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YOD1 attenuates neurogenic proteotoxicity through its deubiquitinating activity von Tanji, Kunikazu, Mori, Fumiaki, Miki, Yasuo, Utsumi, Jun, Sasaki, Hidenao, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Alteration of Upstream Autophagy-Related Proteins (ULK1, ULK2, Beclin1, VPS34 and AMBRA1) in Lewy Body Disease von Miki, Yasuo, Tanji, Kunikazu, Mori, Fumiaki, Utsumi, Jun, Sasaki, Hidenao, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy von Miki, Yasuo, Tsushima, Eiki, Foti, Sandrine C., Strand, Kate M., Asi, Yasmine T., Yamamoto, Adam Kenji, Bettencourt, Conceicao, Oliveira, Marcos C. B., De Pablo-Fernandez, Eduardo, Jaunmuktane, Zane, Lees, Andrew J., Wakabayashi, Koichi, Warner, Thomas T., Quinn, Niall, Holton, Janice L., Ling, Helen

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The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality von Miki, Yasuo, Kamata, Kosuke, Goto, Shintaro, Sakuraba, Hirotake, Mori, Fumiaki, Yamagata, Kazufumi, Kijima, Hiroshi, Fukuda, Shinsaku, Wakabayashi, Koichi

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Accumulation of the sigma-1 receptor is common to neuronal nuclear inclusions in various neurodegenerative diseases von Miki, Yasuo, Mori, Fumiaki, Kon, Tomoya, Tanji, Kunikazu, Toyoshima, Yasuko, Yoshida, Mari, Sasaki, Hidenao, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Behavioral and histological analyses of the mouse Bassoon p.P3882A mutation corresponding to the human BSN p.P3866A mutation von Tanaka, Daiki, Yaguchi, Hiroaki, Yoshizaki, Kaichi, Kudo, Akihiko, Mori, Fumiaki, Nomura, Taichi, Pan, Jing, Miki, Yasuo, Takahashi, Hidehisa, Hara, Taichi, Wakabayashi, Koichi, Yabe, Ichiro

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