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

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Glucose, Fructose, and Urate Transporters in the Choroid Plexus Epithelium von Chiba, Yoichi, Murakami, Ryuta, Matsumoto, Koichi, Wakamatsu, Keiji, Nonaka, Wakako, Uemura, Naoya, Yanase, Ken, Kamada, Masaki, Ueno, Masaki

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Novel monoallelic variant in ERLIN2 causes spastic paraplegia converted to amyotrophic lateral sclerosis von Kume, Kodai, Kamada, Masaki, Shimatani, Yoshimitsu, Takata, Tadayuki, Izumi, Yuishin, Kawakami, Hideshi

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Disturbance of Intracerebral Fluid Clearance and Blood-Brain Barrier in Vascular Cognitive Impairment von Ueno, Masaki, Chiba, Yoichi, Murakami, Ryuta, Matsumoto, Koichi, Fujihara, Ryuji, Uemura, Naoya, Yanase, Ken, Kamada, Masaki

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Ascending spinal tract formation in chick embryo originating from different spinal regions von Kokudo, Yohei, Arakawa, Takahiro, Takahashi, Hiroo, Kobara, Hideki, Kamada, Masaki, Deguchi, Kazushi, Touge, Tetsuo, Masaki, Tsutomu, Yamamoto, Tohru

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Analysis of genetic risk factors in Japanese patients with Parkinson's disease von Kanaya, Yuhei, Kume, Kodai, Morino, Hiroyuki, Ohsawa, Ryosuke, Kurashige, Takashi, Kamada, Masaki, Torii, Tsuyoshi, Izumi, Yuishin, Maruyama, Hirofumi, Kawakami, Hideshi

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Optineurin defects cause TDP43-pathology with autophagic vacuolar formation von Kurashige, Takashi, Kuramochi, Masahito, Ohsawa, Ryosuke, Yamashita, Yui, Shioi, Go, Morino, Hiroyuki, Kamada, Masaki, Ayaki, Takashi, Ito, Hidefumi, Sotomaru, Yusuke, Maruyama, Hirofumi, Kawakami, Hideshi

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Acute Intermittent Porphyria Presenting with Posterior Reversible Encephalopathy Syndrome, Accompanied by Prolonged Vasoconstriction von Takata, Tadayuki, Kume, Kodai, Kokudo, Yohei, Ikeda, Kazuyo, Kamada, Masaki, Touge, Tetsuo, Deguchi, Kazushi, Masaki, Tsutomu

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Metabolites and Biomarker Compounds of Neurodegenerative Diseases in Cerebrospinal Fluid von Wakamatsu, Keiji, Chiba, Yoichi, Murakami, Ryuta, Miyai, Yumi, Matsumoto, Koichi, Kamada, Masaki, Nonaka, Wakako, Uemura, Naoya, Yanase, Ken, Ueno, Masaki

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Significance of the hot-cross bun sign on T2-weighted MRI for the diagnosis of multiple system atrophy von Deguchi, Kazushi, Ikeda, Kazuyo, Kume, Kodai, Takata, Tadayuki, Kokudo, Yohei, Kamada, Masaki, Touge, Tetsuo, Honjo, Naomi, Masaki, Tsutomu

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First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China von Naito, Hiroyuki, Takahashi, Tetsuya, Kamada, Masaki, Morino, Hiroyuki, Yoshino, Hiroyo, Hattori, Nobutaka, Maruyama, Hirofumi, Kawakami, Hideshi, Matsumoto, Masayasu

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CSF cystatin C and diffusion tensor imaging parameters as biomarkers of upper motor neuron degeneration in amyotrophic lateral sclerosis von Nakane, Shunya, Fujita, Koji, Azuma, Shingo, Urushihara, Ryo, Kamada, Masaki, Harada, Masafumi, Izumi, Yuishin, Kaji, Ryuji

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Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population von Sugihara, Katsunobu, Maruyama, Hirofumi, Kamada, Masaki, Morino, Hiroyuki, Kawakami, Hideshi

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Dialysis-induced Subdural Hematoma in an Arachnoid Cyst Associated with Autosomal Dominant Polycystic Kidney Disease von Takata, Tadayuki, Kokudo, Yohei, Kume, Kodai, Ikeda, Kazuyo, Kamada, Masaki, Touge, Tetsuo, Deguchi, Kazushi, Masaki, Tsutomu

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Usefulness of the modified F-ratio for assessmentsof proximal conduction in chronic inflammatory demyelinating polyneuropathy superimposed onCharcot Marie–Tooth disease type 1A von Kume, Kodai, Deguchi, Kazushi, Ikeda, Kazuyo, Takata, Tadayuki, Kokudo, Yohei, Kamada, Masaki, Tsukaguchi, Masago, Touge, Tetsuo, Masaki, Tsutomu

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Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation von Kamada, Masaki, Izumi, Yuishin, Ayaki, Takashi, Nakamura, Masataka, Kagawa, Seiko, Kudo, Eiji, Sako, Wataru, Maruyama, Hirofumi, Nishida, Yoshihiko, Kawakami, Hideshi, Ito, Hidefumi, Kaji, Ryuji

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Premedication of hemin for eradication therapy of Helicobacter pylori in patients with porphyria von Takata, Tadayuki, Kokudo, Yohei, Morishita, Asahiro, Kume, Kodai, Yachida, Tatsuo, Kamada, Masaki, Kobara, Hideki, Deguchi, Kazushi, Touge, Tetsuo, Masugata, Hisashi, Masaki, Tsutomu

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Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis von Kamada, Masaki, Maruyama, Hirofumi, Tanaka, Eiji, Morino, Hiroyuki, Wate, Reika, Ito, Hidefumi, Kusaka, Hirofumi, Kawano, Yuji, Miki, Tetsuro, Nodera, Hiroyuki, Izumi, Yuishin, Kaji, Ryuji, Kawakami, Hideshi

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Assessment of sensory perception and processing using current perception threshold in Parkinson's disease von Ikeda, Kazuyo, Deguchi, Kazushi, Kume, Kodai, Kamada, Masaki, Touge, Tetsuo, Masaki, Tsutomu

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Ocular myasthenia gravis with anti-muscle-specific tyrosine kinase antibodies: Two new cases and a systematic literature review von Kamada, Masaki, Nakane, Shunya, Matsui, Naoko, Higuchi, Osamu, Sakai, Waka, Fujita, Koji, Izumi, Yuishin, Matsuo, Hidenori, Kaji, Ryuji

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