Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy von Katsuno, Masahisa, Adachi, Hiroaki, Doyu, Manabu, Minamiyama, Makoto, Sang, Chen, Kobayashi, Yasushi, Inukai, Akira, Sobue, Gen

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Analysis of medication and prescription background risk factors contributing to oral medication administration errors by nurses: A case–control study von Suzuki, Ryohei, Sakai, Takamasa, Kato, Mariyo, Takahashi, Masaaki, Inukai, Akira, Ohtsu, Fumiko

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Myopathy in thiamine deficiency: Analysis of a case von Koike, Haruki, Watanabe, Hirohisa, Inukai, Akira, Iijima, Masahiro, Mori, Keiko, Hattori, Naoki, Sobue, Gen

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17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration von Waza, Masahiro, Adachi, Hiroaki, Katsuno, Masahisa, Minamiyama, Makoto, Sang, Chen, Tanaka, Fumiaki, Inukai, Akira, Doyu, Manabu, Sobue, Gen

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A case of M232R genetic Creutzfeldt-Jakob disease with Lewy bodies von Akagi, Akio, Iwasaki, Yasushi, Hashimoto, Rina, Aiba, Ikuko, Inukai, Akira, Mimuro, Maya, Riku, Yuichi, Miyahara, Hiroaki, Kitamoto, Tetsuyuki, Yoshida, Mari

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Tissue-Specific Somatic Mosaicism in Spinal and Bulbar Muscular Atrophy Is Dependent on CAG-Repeat Length and Androgen Receptor–Gene Expression Level von Tanaka, Fumiaki, Reeves, Matthew F., Ito, Yasuhiro, Matsumoto, Michiyo, Li, Mei, Miwa, Shigeru, Inukai, Akira, Yamamoto, Masahiko, Doyu, Manabu, Yoshida, Mari, Hashizume, Yoshio, Terao, Shin-ichi, Mitsuma, Terunori, Sobue, Gen

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Clinical and imaging findings of progressive supranuclear palsy with predominant cerebellar ataxia von Shimohata, Takayoshi, Kanazawa, Masato, Yoshida, Mari, Saito, Yufuko, Iwai, Katsushige, Yasuda, Takeshi, Inukai, Akira, Takahashi, Hitoshi, Nishizawa, Masatoyo, Aiba, Ikuko

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Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy von Katsuno, Masahisa, Adachi, Hiroaki, Doyu, Manabu, Minamiyama, Makoto, Sang, Chen, Kobayashi, Yasushi, Inukai, Akira, Sobue, Gen

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The role of lymphotoxin in pathogenesis of polymyositis von YIDENG LIANG, INUKAI, A, KURU, S, KATO, T, DOYU, M, SOBUE, G

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Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan von Sobue, Gen, Koike, Haruki, Misu, Ken-ichiro, Hattori, Naoki, Yamamoto, Masahiko, Ikeda, Shu-ichi, Ando, Yukio, Nakazato, Masamitsu, Inukai, Akira

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Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients von Adachi, Hiroaki, Katsuno, Masahisa, Minamiyama, Makoto, Waza, Masahiro, Sang, Chen, Nakagomi, Yuji, Kobayashi, Yasushi, Tanaka, Fumiaki, Doyu, Manabu, Inukai, Akira, Yoshida, Mari, Hashizume, Yoshio, Sobue, Gen

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High titer of ADAMTS13 inhibitor associated with thrombotic microangiopathy of the gut and skeletal muscle after allogeneic hematopoietic stem cell transplantation von Adachi, Tatsuya, Matsushita, Tadashi, Ichihashi, Ryoichi, Hirashima, Kanji, Ito, Masafumi, Inukai, Akira, Yokozawa, Toshiya, Nishida, Tetsuya, Murata, Makoto, Hayashi, Mutsuharu, Katsumi, Akira, Kojima, Tetsuhito, Saito, Hidehiko, Naoe, Tomoki

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An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy von Iwasaki, Yasushi, Hashimoto, Rina, Saito, Yufuko, Aiba, Ikuko, Inukai, Akira, Akagi, Akio, Mimuro, Maya, Miyahara, Hiroaki, Kitamoto, Tetsuyuki, Yoshida, Mari

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The characteristics of camptocormia in patients with Parkinson's disease: A large cross-sectional multicenter study in Japan von Nakane, Shunya, Yoshioka, Masaru, Oda, Nobuhito, Tani, Takashi, Chida, Keiji, Suzuki, Mikiya, Funakawa, Itaru, Inukai, Akira, Hasegawa, Kazuko, Kuroda, Kenji, Mizoguchi, Kouichi, Shioya, Keiichi, Sonoda, Yoshito, Matsuo, Hidenori

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Expression of HLA-DR and its enhancing molecules in muscle fibers in polymyositis von Inukai, Akira, Kuru, Satosi, Liang, Yideng, Takano, Akemi, Kobayashi, Yasushi, Sakai, Motoko, Doyu, Manabu, Sobue, Gen

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Transdermal rotigotine in early stage Parkinson's disease: A randomized, double-blind, placebo-controlled trial von Mizuno, Yoshikuni, Nomoto, Masahiro, Kondo, Tomoyoshi, Hasegawa, Kazuko, Murata, Miho, Takeuchi, Masahiro, Ikeda, Junji, Tomida, Takayuki, Hattori, Nobutaka

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Expression of tumor necrosis factor-α in regenerating muscle fibers in inflammatory and non-inflammatory myopathies von KURU, Satoshi, INUKAI, Akira, KATO, Takashi, YIDENG LIANG, KIMURA, Seigo, SOBUE, Gen

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Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy von Minamiyama, Makoto, Katsuno, Masahisa, Adachi, Hiroaki, Waza, Masahiro, Sang, Chen, Kobayashi, Yasushi, Tanaka, Fumiaki, Doyu, Manabu, Inukai, Akira, Sobue, Gen

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Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan : Clinicopathological and gen... von MISU, K.-I, HATTORI, N, HARADA, T, INUKAI, A, HASHIZUME, Y, SOBUE, G, NAGAMATSU, M, IKEDA, S.-I, ANDO, Y, NAKAZATO, M, TAKEI, Y.-I, HANYU, N, USUI, Y, TANAKA, F

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A case of rapidly progressive syringomyelia due to a spinal hemangioblastoma von Sakakibara, Satoko, Tamura, Takuya, Katayama, Taiji, Saito, Yufuko, Aiba, Ikuko, Inukai, Akira

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