Distribution of cerebello-olivary degeneration in idiopathic late cortical cerebellar atrophy: Clinicopathological study of four autopsy cases von Ota, Satoru, Tsuchiya, Kuniaki, Anno, Midori, Niizato, Kazuhiro, Akiyama, Haruhiko

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Gray matter lesions in Nasu-Hakola disease: A report on three autopsy cases von Aoki, Naoya, Tsuchiya, Kuniaki, Togo, Takashi, Kobayashi, Zen, Uchikado, Hirotake, Katsuse, Omi, Suzuki, Kyoko, Fujishiro, Hiroshige, Arai, Tetsuaki, Iseki, Eizo, Anno, Midori, Kosaka, Kenji, Akiyama, Haruhiko, Hirayasu, Yoshio

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SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein von Nakamura, K, Jeong, S Y, Uchihara, T, Anno, M, Nagashima, K, Nagashima, T, Ikeda, S, Tsuji, S, Kanazawa, I

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Ultrastructural characterization of the tau-immunoreactive tubules in the oligodendroglial perikarya and their inner loop processes in progressive supranuclear palsy von ARIMA, K, NAKAMURA, M, SUNOHARA, N, OGAWA, M, ANNO, M, IZUMIYAMA, Y, HIRAI, S, IKEDA, K

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Parkinson's disease mimicking senile dementia of the Alzheimer type: a clinicopathological study of four autopsy cases von Tsuchiya, Kuniaki, Ikeda, Kenji, Niizato, Kazuhiro, Watabiki, Sadakiyo, Anno, Midori, Taki, Kazuhiro, Haga, Chie, Iritani, Shuji, Matsushita, Masaaki

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SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein von NAKAMURA, Koichiro, JEONG, Seon-Yong, UCHIHARA, Toshiki, ANNO, Midori, NAGASHIMA, Kazuo, NAGASHIMA, Toshiko, IKEDA, Shu-Ichi, TSUJI, Shoji, KANAZAWA, Ichiro

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A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology von Kobayashi, Tomonori, Ota, Satoru, Tanaka, Kuniaki, Ito, Yuji, Hasegawa, Masato, Umeda, Yuri, Motoi, Yumiko, Takanashi, Masashi, Yasuhara, Masahiro, Anno, Midori, Mizuno, Yoshikuni, Mori, Hideo

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Gray matter lesions in Nasu-Hakola disease: A report on three autopsy cases: Gray matter lesions in Nasu-Hakola disease von Aoki, Naoya, Tsuchiya, Kuniaki, Togo, Takashi, Kobayashi, Zen, Uchikado, Hirotake, Katsuse, Omi, Suzuki, Kyoko, Fujishiro, Hiroshige, Arai, Tetsuaki, Iseki, Eizo, Anno, Midori, Kosaka, Kenji, Akiyama, Haruhiko, Hirayasu, Yoshio

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Gray matter lesions in NasuaHakola disease: A report on three autopsy cases von Aoki, Naoya, Tsuchiya, Kuniaki, Togo, Takashi, Kobayashi, Zen, Uchikado, Hirotake, Katsuse, Omi, Suzuki, Kyoko, Fujishiro, Hiroshige, Arai, Tetsuaki, Iseki, Eizo, Anno, Midori, Kosaka, Kenji, Akiyama, Haruhiko, Hirayasu, Yoshio

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Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17 von KOBAYASHI, Tomonori, MORI, Hideo, NARABAYASHI, Hirotaro, MIZUNO, Yoshikuni, OKUMA, Yasuyuki, DICKSON, Dennis W, COOKSON, Natalie, TSUBOI, Yoshio, MOTOI, Yumiko, TANAKA, Ryota, MIYASHITA, Nobuo, ANNO, Midori

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A case of frontotemporal dementia with tau P301L mutation in the Far East von Tanaka, R, Kobayashi, T, Motoi, Y, Anno, M, Mizuno, Y, Mori, H

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Effects of paraquat on mitochondria of rat skeletal muscle von Yamamoto, Takeshi, Anno, Midori, Sato, Takeshi

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