Resveratrol improves motor function in patients with muscular dystrophies: an open-label, single-arm, phase IIa study von Kawamura, Kentaro, Fukumura, Shinobu, Nikaido, Koki, Tachi, Nobutada, Kozuka, Naoki, Seino, Tsugumi, Hatakeyama, Kingya, Mori, Mitsuru, Ito, Yoichi M., Takami, Akiyoshi, Hinotsu, Shiro, Kuno, Atsushi, Kawasaki, Yukihiko, Horio, Yoshiyuki, Tsutsumi, Hiroyuki

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The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin von Koenig, Michel, Gibson, Toby, Barbot, Clara, Yanagisawa, Takayuki, Mendonça, Pedro, Costa, Manuela, Moreira, Maria-Céu, Aoki, Masashi, Coutinho, Paula, Uchida, Eiji, Ikeda, Yoshio, Watanabe, Mitsunori, Barros, José, Tachi, Nobutada, Sequeiros, Jorge, Kozuka, Naoki, Nagata, Tetsuya

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New mutation of CACNA1A gene in episodic ataxia type 2 von Nikaido, Koki, Tachi, Nobutada, Ohya, Kazuhiro, Wada, Takahito, Tsutsumi, Hiroyuki

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Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity von Moreira, Maria do Céu, Barbot, Clara, Tachi, Nobutada, Kozuka, Naoki, Mendonça, Pedro, Barros, José, Coutinho, Paula, Sequeiros, Jorge, Koenig, Michel

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The acid-sensing ion channel 2 (ASIC2) of ciliated cells in the developing rat nasal septum von Kikuchi, Shin, Ninomiya, Takafumi, Kawamata, Tomoyuki, Ogasawara, Noriko, Kojima, Takashi, Tachi, Nobutada, Tatsumi, Haruyuki

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Carbamazepine-Induced Hemolytic and Aplastic Crises Associated with Reduced Glutathione Peroxidase Activity of Erythrocytes von YAMAMOTO, Masaki, SUZUKI, Nobuhiro, HATAKEYAMA, Naoki, KUBO, Noriaki, TACHI, Nobutada, KANNO, Hitoshi, FUJII, Hisaichi, TSUTSUMI, Hiroyuki

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New Mutation of the PTCH Gene in Nevoid Basal-Cell Carcinoma Syndrome With West Syndrome von Tachi, Nobutada, MD, PhD, Fujii, Katsunori, MD, PhD, Kimura, Mitsugu, MD, Seki, Kouhei, MD, PhD, Hirakai, Masahisa, MD, PhD, Miyashita, Toshiyuki, MD, PhD

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Study of Visual Function Evaluation for People with Severe Motor and Intellectual Disabilities Utilizing Near-Infrared Spectroscopy von Nakamura, Yuji, Sengoku, Yasuhito, Nakajima, Sonomi, Ohyanagi, Toshio, Sugama, Kosuke, Horimoto, Yositaka, Tachi, Nobutada

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De novo mutation of the myelin Po gene in Dejerine–Sottas disease (hereditary motor and sensory neuropathy type III) von Hayasaka, Kiyoshi, Himoro, Masato, Sawaishi, Yukio, Nanao, Kenji, Takahashi, Tsutomu, Takada, Goro, Nicholson, Garth A., Ouvrier, Robert A., Tachi, Nobutada

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The Change of Grip Strength in a Patient with Congenital Myotonic Dystrophy Over a 4-year Period von Kikuchi, Shin, Kozuka, Naoki, Uchida, Eiji, Ninomiya, Takafumi, Tatsumi, Haruyuki, Takeda, Hidekatsu, Tachi, Nobutada

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A myotonic dystrophy 1 patient complicated with placental adherence after miscarriage of one dichorionic diamniotic twin following her tenth in vitro fertilization and embryo trans... von Endo, Toshiaki, Baba, Tsuyoshi, Sugio, Asuka, Morishita, Miyuki, Takahashi, Madoka, Akashi, Yushi, Ishioka, Shinichi, Tachi, Nobutada, Imai, Tomihiro, Tamakawa, Mitsuharu, Saito, Tsuyoshi

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Infant botulism due to Clostridium botulinum type C toxin von Oguma, Keiji, Yokota, Kenji, Hayashi, Shunji, Takeshi, Koichi, Kumagai, Mitsuru, Itoh, Nozomi, Tachi, Nobutada, Chiba, Shunzo

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Molecular and pathological studies in Charcot-Marie-Tooth disease 1A von Kozuka, Naoki, Tachi, Nobutada, Ohya, Kazuhiro, Chiba, Shunzo

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The Change of Grip Strength in a Patient with Congenital Myotonic Dystrophy Over a 4-year Period von Shin KIKUCHI, Naoki KOZUKA, Eiji UCHIDA, Takafumi NINOMIYA, Haruyuki TATSUMI, Hidekatsu TAKEDA, Nobutada TACHI

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Detection of the CTG repeat expansion in congenital myotonic dystrophy von Ohya, Kazuhiro, Tachi, Nobutada, Sato, Toshiya, Kon, Shinichiro, Kikuchi, Kokichi, Chiba, Shunzo

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A new mutation of IGHMBP2 gene in spinal muscular atrophy with respiratory distress type 1 von Tachi, Nobutada, Kikuchi, Sin, Kozuka, Naoki, Nogami, Azusa

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The appearance of aprataxin in rat cultured neuron and glia von Ninomiya, Takafumi, Kikuchi, Shin, Ichikawa, Ryoichi, Kozuka, Naoki, Tachi, Nobutada, Tatsumi, Haruyuki

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Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination von LOPES, J, RAVISE, N, LATOUR, P, RUBERG, M, BRICE, A, LEGUERN, E, VANDENBERGHE, A, PALAU, F, IONASESCU, V, MAYER, M, LEVY, N, WOOD, N, TACHI, N, BOUCHE, P

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Immunocytochemical Localization of Myotonic Dystrophy Protein Kinase in Cultured Muscle von Tachi, Nobutada, Watanabe, Yukie, Kozuka, Naoki, Ohya, Kazuhiro, Chiba, Sunzo

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Clinicopathological and virological analyses of familial human T-lymphotropic virus type I-associated polyneuropathy von Sawa, Hirofumi, Nagashima, Toshiko, Nagashima, Kazuo, Shinihara, Toshiya, Chuma, Takayo, Mano, Yukio, Tachi, Nobutada, Hall, William W

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