First Japanese autopsy case showing LRRK2 mutation G2019S and TDP-43 proteinopathy von Sakuwa, Mayuko, Adachi, Tadashi, Suzuki, Yuki, Yoshida, Kentaro, Fukuda, Hiroki, Miura, Hiroshi, Adachi, Yoshiki, Hanajima, Ristuko

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An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α‐synucleinopathy von Sakuwa, Mayuko, Adachi, Tadashi, Yoshida, Kentaro, Adachi, Yoshiki, Nakano, Toshiya, Hanajima, Ritsuko

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Cognitive and behavioral status in Japanese ALS patients: a multicenter study von Watanabe, Yasuhiro, Raaphorst, Joost, Izumi, Yuishin, Yoshino, Hiide, Ito, Satoru, Adachi, Tadashi, Takigawa, Hiroshi, Masuda, Michihito, Atsuta, Naoki, Adachi, Yoshiki, Isose, Sagiri, Arai, Kimihito, Yokota, Osamu, Oda, Masaya, Ogino, Mieko, Ichikawa, Hiroo, Hasegawa, Kazuko, Kimura, Hideki, Shimizu, Toshio, Aiba, Ikuko, Yabe, Hayato, Kanba, Makoto, Kusumi, Kimiyoshi, Aoki, Tetsuya, Hiroe, Yu, Watanabe, Hirohisa, Nishiyama, Kazutoshi, Nomoto, Masahiro, Sobue, Gen, Beeldman, Emma, Hanajima, Ritsuko, Nakashima, Kenji

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The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins von Sawada, Jun, Katayama, Takayuki, Tokashiki, Takashi, Kikuchi, Shiori, Kano, Kohei, Takahashi, Kae, Saito, Tsukasa, Adachi, Yoshiki, Okamoto, Yuji, Yoshimura, Akiko, Takashima, Hiroshi, Hasebe, Naoyuki

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Autopsy case of spinocerebellar ataxia type 31 with severe dementia at the terminal stage von Adachi, Tadashi, Kitayama, Michio, Nakano, Toshiya, Adachi, Yoshiki, Kato, Shinsuke, Nakashima, Kenji

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A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan von Yasui, Kenichi, Yabe, Ichiro, Yoshida, Kunihiro, Kanai, Kazuaki, Arai, Kimihito, Ito, Mizuki, Onodera, Osamu, Koyano, Shigeru, Isozaki, Eiji, Sawai, Setsu, Adachi, Yoshiki, Sasaki, Hidenao, Kuwabara, Satoshi, Hattori, Takamichi, Sobue, Gen, Mizusawa, Hidehiro, Tsuji, Shoji, Nishizawa, Masatoyo, Nakashima, Kenji

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Japanese version of the ALS-FTD-questionnaire (ALS-FTD-Q-J) von Watanabe, Yasuhiro, Beeldman, Emma, Raaphorst, Joost, Izumi, Yuishin, Yoshino, Hiide, Masuda, Michihito, Atsuta, Naoki, Ito, Satoru, Adachi, Tadashi, Adachi, Yoshiki, Yokota, Osamu, Oda, Masaya, Hanashima, Ritsuko, Ogino, Mieko, Ichikawa, Hiroo, Hasegawa, Kazuko, Kimura, Hideki, Shimizu, Toshio, Aiba, Ikuko, Yabe, Hayato, Kanba, Makoto, Kusumi, Kimiyoshi, Aoki, Tetsuya, Hiroe, Yu, Watanabe, Hirohisa, Nishiyama, Kazutoshi, Nomoto, Masahiro, Sobue, Gen, Nakashima, Kenji

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Repeated Encephalopathy and Hemicerebral Atrophy in a Patient with Familial Hemiplegic Migraine Type 1 von Tashiro, Yuichi, Yamazaki, Tsuneo, Nagamine, Shun, Mizuno, Yuji, Yoshiki, Adachi, Okamoto, Koichi

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Hemiconvulsion-Hemiplegia-Epilepsy Syndrome Associated With CACNA1A S218L Mutation von Yamazaki, Sawako, MD, Ikeno, Kanju, MD, Abe, Tokinari, MD, Tohyama, Jun, MD, Adachi, Yoshiki, MD

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ALS-Parkinsonism-Dementia complex of Kii and other related diseases in Japan von Kaji, Ryuji, Izumi, Yishin, Adachi, Yoshiki, Kuzuhara, Shigeki

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Population-Based Door-to-Door Survey of Migraine in Japan: The Daisen Study von Takeshima, Takao, Ishizaki, Kumiko, Fukuhara, Yoko, Ijiri, Tamami, Kusumi, Masayoshi, Wakutani, Yosuke, Mori, Masatada, Kawashima, Mika, Kowa, Hisanori, Adachi, Yoshiki, Urakami, Katsuya, Nakashima, Kenji

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Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA von Nakaso, Kazuhiro, Adachi, Yoshiki, Fusayasu, Emi, Doi, Koji, Imamura, Keiko, Yasui, Kenichi, Nakashima, Kenji

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Prevalence of Dementia in the Rural Island Town of Ama-cho, Japan von Wada-Isoe, Kenji, Uemura, Yusuke, Suto, Yutaka, Doi, Koji, Imamura, Keiko, Hayashi, Ai, Kitayama, Michio, Watanabe, Yasuhiro, Adachi, Yoshiki, Nakashima, Kenji

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Prevalence of progressive supranuclear palsy in Yonago, Japan von Kawashima, Mika, Miyake, Masahiro, Kusumi, Masayoshi, Adachi, Yoshiki, Nakashima, Kenji

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Corticobasal degeneration with visual hallucination as an initial symptom: A case report von Yoshida, Kentaro, Adachi, Tadashi, Suzuki, Yuki, Sakuwa, Mayuko, Fukuda, Hiroki, Hasegawa, Masato, Adachi, Yoshiki, Miura, Hiroshi, Hanajima, Ritsuko

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Morphological Alterations of the Sarcotubular System in Permanent Myopathy of Hereditary Hypokalemic Periodic Paralysis with a Mutation in the CACNA1S Gene von Nagasaka, Takamura, Hata, Takanori, Shindo, Kazumasa, Adachi, Yoshiki, Takeuchi, Megumi, Saito, Kayoko, Takiyama, Yoshihisa

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Cerebrospinal fluid tau in dementia disorders: a large scale multicenter study by a Japanese study group von Shoji, Mikio, Matsubara, Etsuro, Murakami, Tetsuro, Manabe, Yasuhiro, Abe, Koji, Kanai, Mitsuyasu, Ikeda, Masaki, Tomidokoro, Yasushi, Shizuka, Masami, Watanabe, Mitsunori, Amari, Masakuni, Ishiguro, Koji, Kawarabayashi, Takeshi, Harigaya, Yasuo, Okamoto, Koichi, Nishimura, Tsuyosi, Nakamura, Yu, Takeda, Masatoshi, Urakami, Katsuya, Adachi, Yoshiki, Nakashima, Kenji, Arai, Hiroyuki, Sasaki, Hidetada, Kanemaru, Kazutomi, Yamanouchi, Hiroshi, Yoshida, Yasuji, Ichise, Kunihiro, Tanaka, Kuniaki, Hamamoto, Makoto, Yamamoto, Hideki, Matsubayashi, Takeyuki, Yoshida, Hiroshi, Toji, Hiromasa, Nakamura, Shigenobu, Hirai, Shunsaku

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An Unusual Case of Elderly-Onset Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) With Multiple Cerebrovascular Risk Factors von Watanabe, Mitsunori, MD, PhD, Adachi, Yoshiki, MD, PhD, Jackson, Mandy, DPhil, Yamamoto-Watanabe, Yukiko, MD, Wakasaya, Yasuhito, MD, Shirahama, Ikumi, Takamura, Ayumi, PhD, Matsubara, Etsuro, MD, PhD, Kawarabayashi, Takeshi, MD, PhD, Shoji, Mikio, MD, PhD

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Genetic Analysis of Vascular Factors in Alzheimer's Disease von WAKUTANI, YOSUKE, KOWA, HISANORI, KUSUMI, MASAYOSHI, YAMAGATA, KAORU, WADA-ISOE, KENJI, ADACHI, YOSHIKI, TAKESHIMA, TAKAO, URAKAMI, KATSUYA, NAKASHIMA, KENJI

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Longitudinal changes in the prevalence of dementia in a Japanese rural area von WAKUTANI, Yosuke, KUSUMI, Masayoshi, WADA, Kenji, KAWASHIMA, Mika, ISHIZAKI, Kumiko, MORI, Masatada, MORI, Nozomi, IJIRI, Tamami, ADACHI, Yoshiki, ASHIDA, Yasushi, KUNO, Nobutoshi, URAKAMI, Katsuya, TAKESHIMA, Takao, NAKASHIMA, Kenji

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