A Pilot Study of A2NTX, a Novel Low-Molecular-Weight Neurotoxin Derived from Subtype A2 for Post-Stroke Lower Limb Spasticity: Comparison with OnabotulinumtoxinA von Kaji, Ryuji, Miyashiro, Ai, Sato, Nori, Furumoto, Taiki, Takeuchi, Toshiaki, Miyamoto, Ryosuke, Kohda, Tomoko, Izumi, Yuishin, Kozaki, Shunji

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Clinical Safety and Tolerability of A2NTX, a Novel Low-Molecular-Weight Neurotoxin Derived from Botulinum Neurotoxin Subtype A2, in Comparison with Subtype A1 Toxins von Takeuchi, Toshiaki, Okuno, Tsuyoshi, Miyashiro, Ai, Kohda, Tomoko, Miyamoto, Ryosuke, Izumi, Yuishin, Kozaki, Shunji, Kaji, Ryuji

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MR Spectroscopy in Patients with Hereditary Diffuse Leukoencephalopathy with Spheroids and Asymptomatic Carriers of Colony-stimulating Factor 1 Receptor Mutation von Abe, Takashi, Kawarai, Toshitaka, Fujita, Koji, Sako, Wataru, Terasawa, Yuka, Matsuda, Tsuyoshi, Sakai, Waka, Tsukamoto-Miyashiro, Ai, Matsui, Naoko, Izumi, Yuishin, Kaji, Ryuji, Harada, Masafumi

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Are multifocal motor neuropathy patients underdiagnosed? An epidemiological survey in Japan von Miyashiro, Ai, Matsui, Naoko, Shimatani, Yoshimitsu, Nodera, Hiroyuki, Izumi, Yuishin, Kuwabara, Satoshi, Imai, Tomihiro, Baba, Masayuki, Komori, Tetsuo, Sonoo, Masahiro, Mezaki, Takahiro, Kawamata, Jun, Hitomi, Takefumi, Kohara, Nobuo, Arimura, Kimiyoshi, Hashimoto, Shuji, Arisawa, Kokichi, Kusunoki, Susumu, Kaji, Ryuji

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Treatment and indication of botulinum toxin type A for limb spasticity -Can we break the 6 months barrier? von Miyashiro, Ai

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DYT6 in Japan-genetic screening and clinical characteristics of the patients von Miyamoto, Ryosuke, Koizumi, Hidetaka, Morino, Hiroyuki, Kawarai, Toshitaka, Maruyama, Hirofumi, Mukai, Yohei, Miyashiro, Ai, Sako, Wataru, Izumi, Yuishin, Kawakami, Hideshi, Kaji, Ryuji

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Hyperexcitability as a potential cause for diffuse lower motor neuron loss in Isaacs’ syndrome von Furukawa, Takahiro, Nodera, Hiroyuki, Shimatani, Yoshimitsu, Watanabe, Osamu, Miyashiro, Ai, Mori, Atsuko, Matsui, Naoko, Nishida, Yoshihiko, Izumi, Yuishin, Kaji, Ryuji

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A novel AIFM1 missense mutation in a Japanese patient with ataxic sensory neuronopathy and hearing impairment von Kawarai, Toshitaka, Yamazaki, Hiroki, Yamakami, Kei, Tsukamoto-Miyashiro, Ai, Kodama, Mizuki, Rumore, Roberto, Caltagirone, Carlo, Nishino, Ichizo, Orlacchio, Antonio

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Takotsubo syndrome complicated with amyotrophic lateral sclerosis (P4.056) von Izumi, Yuishin, Miyashiro, Ai, Nodera, Hiroyuki, Nishinaka, Kazuto, Udaka, Fukashi, Nishida, Yoshihiko, Murayama, Shigeo, Kaji, Ryuji

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Diagnostic spectrum of multifocal motor neuropathy von Matsui, Naoko, Miyashiro, Ai, Shimatani, Yoshimitsu, Nodera, Hiroyuki, Izumi, Yuishin, Kuwabara, Satoshi, Baba, Masayuki, Komori, Tetsuo, Sonoo, Masahiro, Mezaki, Takahiro, Kawamata, Jun, Hitomi, Takefumi, Imai, Tomihiro, Kohara, Nobuo, Arimura, Kimiyoshi, Arisawa, Kokichi, Kusunoki, Susumu, Kaji, Ryuji

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Sera from patients with multifocal motor neuropathy disrupt the blood-nerve barrier von Shimizu, Fumitaka, Omoto, Masatoshi, Sano, Yasuteru, Mastui, Naoko, Miyashiro, Ai, Tasaki, Ayako, Maeda, Toshihiko, Koga, Michiaki, Kaji, Ryuji, Kanda, Takashi

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Increased proinflammatory cytokines in sera of patients with multifocal motor neuropathy von Furukawa, Takahiro, Matsui, Naoko, Fujita, Koji, Miyashiro, Ai, Nodera, Hiroyuki, Izumi, Yuishin, Shimizu, Fumitaka, Miyamoto, Katsuichi, Takahashi, Yukitoshi, Kanda, Takashi, Kusunoki, Susumu, Kaji, Ryuji

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Randomised double-blind clinical trial of botulinum toxin subtype A2 (A2NTX) in comparison with subtype A1 (onabotulinumtoxinA) (ClinicalTrials.gov NCT01910363) (P4.333) von Kaji, Ryuji, Miyashiro, Ai, Sato, Nori, Takeuchi, Toshiaki, Kaji, Seiji, Furumoto, Taiki

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Oromandibular dystonia associated with SCA36 von Miyashiro, Ai, Sugihara, Katsunobu, Kawarai, Toshitaka, Miyamoto, Ryosuke, Izumi, Yuishin, Morino, Hiroyuki, Maruyama, Hirofumi, Orlacchio, Antonio, Kawakami, Hideshi, Kaji, Ryuji

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Treatment of spasticity with botulinum toxin von Miyashiro, Ai

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Late-onset spastic paraplegia: Aberrant SPG11 transcripts generated by a novel splice site donor mutation von Kawarai, Toshitaka, Miyamoto, Ryosuke, Mori, Atsuko, Oki, Ryosuke, Tsukamoto-Miyashiro, Ai, Matsui, Naoko, Miyazaki, Yoshimichi, Orlacchio, Antonio, Izumi, Yuishin, Nishida, Yoshihiko, Kaji, Ryuji

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P2-4 Time course of hypertrophy in cervical nerve roots and peripheral nerves and high-echoic structure signs in cervical nerve roots of CIDP patients von Ai Miyashiro

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Generalized dystonia in a patient with a novel mutation in the GLUD1 gene von Miyamoto, Ryosuke, Goto, Satoshi, Sako, Wataru, Miyashiro, Ai, Kim, Isabelle, Escande, Fabienne, Harada, Masafumi, Morigaki, Ryoma, Asanuma, Kotaro, Mizobuchi, Yoshifumi, Nagahiro, Shinji, Izumi, Yuishin, Kaji, Ryuji

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A case of cerebral air embolism developed during pleural lavage von Miyashiro, Ai, Terasawa, Yuka, Yamamoto, Nobuaki, Izumi, Yuishin, Kaji, Ryuji

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A case of sarcoidosis detected by muscle ultrasonography von TAKAMATSU, Naoko, TERASAWA, Yuka, SAKAI, Waka, MIYAMOTO, Ryosuke, MIYASHIRO, Ai, SHIMATANI, Yoshimitsu, SATOU, Kenta, MATSUI, Naoko, IZUMI, Yuishin, KAJI, Ryuji

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