DISASTER PREVENTION SUPPORT SYSTEM von FURUTO TAKASHI, NAITO KAZUHIRO, ICHINOSE YOSHIHISA, SASAKI MITSUAKI, GOTO SHIGEO, OKI TAKEHIRO, KAKUMOTO SHIGERU, YAMADA HIROYUKI

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RFC1 repeat expansion in Japanese patients with late-onset cerebellar ataxia von Tsuchiya, Mai, Nan, Haitian, Koh, Kishin, Ichinose, Yuta, Gao, Lihua, Shimozono, Keisuke, Hata, Takanori, Kim, Yeon-Jeong, Ohtsuka, Toshihisa, Cortese, Andrea, Takiyama, Yoshihisa

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Hydrophilic amorphous crosslinked membranes with subnanometer pores prepared by plasma-enhanced chemical vapor deposition and their shape-selective alcohol permeation von Samitsu, Sadaki, Ismail, Edhuan, Fujii, Yoshihisa, Ichinose, Izumi

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Flash freezing route to mesoporous polymer nanofibre networks von Samitsu, Sadaki, Zhang, Rui, Peng, Xinsheng, Krishnan, Mohan Raj, Fujii, Yoshihisa, Ichinose, Izumi

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Variants in saposin D domain of prosaposin gene linked to Parkinson's disease von Oji, Yutaka, Hatano, Taku, Ueno, Shin-Ichi, Funayama, Manabu, Ishikawa, Kei-Ichi, Okuzumi, Ayami, Noda, Sachiko, Sato, Shigeto, Satake, Wataru, Toda, Tatsushi, Li, Yuanzhe, Hino-Takai, Tomoko, Kakuta, Soichiro, Tsunemi, Taiji, Yoshino, Hiroyo, Nishioka, Kenya, Hattori, Tatsuya, Mizutani, Yasuaki, Mutoh, Tatsuro, Yokochi, Fusako, Ichinose, Yuta, Koh, Kishin, Shindo, Kazumasa, Takiyama, Yoshihisa, Hamaguchi, Tsuyoshi, Yamada, Masahito, Farrer, Matthew J, Uchiyama, Yasuo, Akamatsu, Wado, Wu, Yih-Ru, Matsuda, Junko, Hattori, Nobutaka

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Mechanically Induced Opening–Closing Action of Binaphthyl Molecular Pliers: Digital Phase Transition versus Continuous Conformational Change von Mori, Taizo, Ishikawa, Daisuke, Yonamine, Yusuke, Fujii, Yoshihisa, Hill, Jonathan P., Ichinose, Izumi, Ariga, Katsuhiko, Nakanishi, Waka

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Clinical and Genetic Study of the First Japanese FTDP-17 Patient with a Mutation of +3 in Intron 10 in the MAPT Gene von Nan, Haitian, Takaki, Ryusuke, Shimozono, Keisuke, Ichinose, Yuta, Koh, Kishin, Takiyama, Yoshihisa

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Clinical characteristics and outcomes of acquired hemophilia A: experience at a single center in Japan von Ogawa, Yoshiyuki, Yanagisawa, Kunio, Uchiumi, Hideki, Ishizaki, Takuma, Mitsui, Takeki, Gouda, Fumito, Ieko, Masahiro, Ichinose, Akitada, Nojima, Yoshihisa, Handa, Hiroshi

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A Japanese SPG4 Patient with a Confirmed De Novo Mutation of the SPAST Gene von Nan, Haitian, Okamoto, Kensho, Gao, Lihua, Morishima, Yuto, Ichinose, Yuta, Koh, Kishin, Hashiyada, Masaki, Adachi, Noboru, Takiyama, Yoshihisa

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Ultrathin free-standing membranes from metal hydroxide nanostrands von Karan, Santanu, Wang, Qifeng, Samitsu, Sadaki, Fujii, Yoshihisa, Ichinose, Izumi

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Dopamine or biopterin deficiency potentiates phosphorylation at 40Ser and ubiquitination of tyrosine hydroxylase to be degraded by the ubiquitin proteasome system von Kawahata, Ichiro, Ohtaku, Shiori, Tomioka, Yoshihisa, Ichinose, Hiroshi, Yamakuni, Tohru

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Exome Sequencing Reveals a Novel Homozygous Frameshift Mutation in the CYP7B1 Gene in a Japanese Patient with SPG5 von Nan, Haitian, Shimozono, Keisuke, Ichinose, Yuta, Tsuchiya, Mai, Koh, Kishin, Hiraide, Masaki, Takiyama, Yoshihisa

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Hydrophilic polymer nanofibre networks for rapid removal of aromatic compounds from water von Krishnan, Mohan Raj, Samitsu, Sadaki, Fujii, Yoshihisa, Ichinose, Izumi

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Impact of the Oral Adsorbent AST-120 on Organ-Specific Accumulation of Uremic Toxins: LC-MS/MS and MS Imaging Techniques von Sato, Emiko, Saigusa, Daisuke, Mishima, Eikan, Uchida, Taeko, Miura, Daisuke, Morikawa-Ichinose, Tomomi, Kisu, Kiyomi, Sekimoto, Akiyo, Saito, Ritsumi, Oe, Yuji, Matsumoto, Yotaro, Tomioka, Yoshihisa, Mori, Takefumi, Takahashi, Nobuyuki, Sato, Hiroshi, Abe, Takaaki, Niwa, Toshimitsu, Ito, Sadayoshi

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Novel GARS mutation presenting as autosomal dominant intermediate Charcot‐Marie‐Tooth disease von Nan, Haitian, Takaki, Ryusuke, Hata, Takanori, Ichinose, Yuta, Tsuchiya, Mai, Koh, Kishin, Takiyama, Yoshihisa

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Increased production of inflammatory cytokines and activation of microglia in the fetal brain of preeclamptic mice induced by angiotensin II von Katoh, Yoshihisa, Iriyama, Takayuki, Yano, Eriko, Sayama, Seisuke, Seyama, Takahiro, Kotajima-Murakami, Hiroko, Sato, Atsushi, Sakuma, Hiroshi, Iguchi, Yoshinobu, Yoshikawa, Midori, Inaoka, Naoko, Ichinose, Mari, Toshimitsu, Masatake, Sone, Kenbun, Kumasawa, Keiichi, Nagamatsu, Takeshi, Ikeda, Kazutaka, Osuga, Yutaka

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Conjugal multiple system atrophy: Computing chance or investigating real patients? von Nan, Haitian, Natori, Takahiro, Ichinose, Yuta, Koh, Kishin, Takiyama, Yoshihisa

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Conjugal multiple system atrophy: Be cautious when calculating numbers of probability von Nan, Haitian, Natori, Takahiro, Ichinose, Yuta, Koh, Kishin, Takiyama, Yoshihisa

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Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment von Koh, Kishin, Ishiura, Hiroyuki, Beppu, Minako, Shimazaki, Haruo, Ichinose, Yuta, Mitsui, Jun, Kuwabara, Satoshi, Tsuji, Shoji, Takiyama, Yoshihisa

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VPS13D‐related disorders presenting as a pure and complicated form of hereditary spastic paraplegia von Koh, Kishin, Ishiura, Hiroyuki, Shimazaki, Haruo, Tsutsumiuchi, Michiko, Ichinose, Yuta, Nan, Haitian, Hamada, Shun, Ohtsuka, Toshihisa, Tsuji, Shoji, Takiyama, Yoshihisa

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