Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability
Li, Jialin, Suda, Kojiro, Ueoka, Ibuki, Tanaka, Ryo, Yoshida, Hideki, Okada, Yasushi, Okamoto, Yuji, Hiramatsu, Yu, Takashima, Hiroshi, Yamaguchi, Masamitsu
Published in Experimental cell research (15.06.2019)
Published in Experimental cell research (15.06.2019)
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Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes
Hiramatsu, Yu, Okamoto, Yuji, Yoshimura, Akiko, Yuan, Jun-Hui, Ando, Masahiro, Higuchi, Yujiro, Hashiguchi, Akihiro, Matsuura, Eiji, Nozaki, Fumihito, Kumada, Tomohiro, Murayama, Kei, Suzuki, Mikiya, Yamamoto, Yuki, Matsui, Naoko, Miyazaki, Yoshimichi, Yamaguchi, Masamitsu, Suzuki, Youji, Mitsui, Jun, Ishiura, Hiroyuki, Tanaka, Masaki, Morishita, Shinichi, Nishino, Ichizo, Tsuji, Shoji, Takashima, Hiroshi
Published in Journal of neurology (01.08.2022)
Published in Journal of neurology (01.08.2022)
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Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan
Yuan, Jun-Hui, Higuchi, Yujiro, Hashiguchi, Akihiro, Ando, Masahiro, Yoshimura, Akiko, Nakamura, Tomonori, Hiramatsu, Yu, Sakiyama, Yusuke, Takashima, Hiroshi
Published in Frontiers in neurology (26.01.2023)
Published in Frontiers in neurology (26.01.2023)
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An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families
Ando, Masahiro, Higuchi, Yujiro, Okamoto, Yuji, Yuan, Junhui, Yoshimura, Akiko, Takei, Jun, Taniguchi, Takaki, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Matsuura, Eiji, Nakagawa, Hiroto, Sonoda, Ken, Yamashita, Toru, Tamura, Akiko, Terasawa, Hideo, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi
Published in Journal of human genetics (01.07.2022)
Published in Journal of human genetics (01.07.2022)
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Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan
Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui H., Yoshimura, Akiko, Higashi, Shuntaro, Takeuchi, Mika, Hobara, Takahiro, Kojima, Fumikazu, Noguchi, Yutaka, Takei, Jun, Hiramatsu, Yu, Nozuma, Satoshi, Sakiyama, Yusuke, Hashiguchi, Akihiro, Matsuura, Eiji, Okamoto, Yuji, Nagai, Masahiro, Takashima, Hiroshi
Published in Frontiers in neurology (10.08.2022)
Published in Frontiers in neurology (10.08.2022)
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Neuron-specific knockdown of Drosophila PDHB induces reduction of lifespan, deficient locomotive ability, abnormal morphology of motor neuron terminals and photoreceptor axon targeting
Dung, Vuu My, Suong, Dang Ngoc Anh, Okamaoto, Yuji, Hiramatsu, Yu, Thao, Dang Thi Phuong, Yoshida, Hideki, Takashima, Hiroshi, Yamaguchi, Masamitsu
Published in Experimental cell research (15.05.2018)
Published in Experimental cell research (15.05.2018)
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Anti-ganglionic acetylcholine receptor antibodies in functional neurological symptom disorder/conversion disorder
Nagata, Ryusei, Matsuura, Eiji, Nozuma, Satoshi, Dozono, Mika, Noguchi, Yutaka, Ando, Masahiro, Hiramatsu, Yu, Kodama, Daisuke, Tanaka, Masakazu, Kubota, Ryuji, Yamakuchi, Munekazu, Higuchi, Yujiro, Sakiyama, Yusuke, Arata, Hitoshi, Higashi, Keiko, Hashiguchi, Teruto, Nakane, Shunya, Takashima, Hiroshi
Published in Frontiers in neurology (13.02.2023)
Published in Frontiers in neurology (13.02.2023)
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Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan
Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui, Yoshimura, Akiko, Kojima, Fumikazu, Yamanishi, Yuki, Aso, Yasuhiro, Izumi, Kotaro, Imada, Minako, Maki, Yoshimitsu, Nakagawa, Hiroto, Hobara, Takahiro, Noguchi, Yutaka, Takei, Jun, Hiramatsu, Yu, Nozuma, Satoshi, Sakiyama, Yusuke, Hashiguchi, Akihiro, Matsuura, Eiji, Okamoto, Yuji, Takashima, Hiroshi
Published in Annals of clinical and translational neurology (01.01.2024)
Published in Annals of clinical and translational neurology (01.01.2024)
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Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible
Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui, Yoshimura, Akiko, Taniguchi, Takaki, Kojima, Fumikazu, Noguchi, Yutaka, Hobara, Takahiro, Takeuchi, Mika, Takei, Jun, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Okamoto, Yuji, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi
Published in Biomedicines (29.06.2022)
Published in Biomedicines (29.06.2022)
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Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan
Ando, Masahiro, Higuchi, Yujiro, Yuan, Jun‐Hui, Yoshimura, Akiko, Kitao, Ruriko, Morimoto, Takehiko, Taniguchi, Takaki, Takeuchi, Mika, Takei, Jun, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Okamoto, Yuji, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi
Published in Annals of clinical and translational neurology (01.05.2022)
Published in Annals of clinical and translational neurology (01.05.2022)
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Efficacy of l‐Arginine treatment in patients with HTLV‐1‐associated neurological disease
Nozuma, Satoshi, Matsuura, Eiji, Tashiro, Yuichi, Nagata, Ryusei, Ando, Masahiro, Hiramatsu, Yu, Higuchi, Yujiro, Sakiyama, Yusuke, Hashiguchi, Akihiro, Michizono, Kumiko, Higashi, Keiko, Matsuzaki, Toshio, Kodama, Daisuke, Tanaka, Masakazu, Yamano, Yoshihisa, Moritoyo, Takashi, Kubota, Ryuji, Takashima, Hiroshi
Published in Annals of clinical and translational neurology (01.02.2023)
Published in Annals of clinical and translational neurology (01.02.2023)
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Toxocara canis myelitis involving the lumbosacral region: a case report
Hiramatsu, Yu, Yoshimura, Michiyoshi, Saigo, Ryuji, Arata, Hitoshi, Okamoto, Yuji, Matsuura, Eiji, Maruyama, Haruhiko, Takashima, Hiroshi
Published in The journal of spinal cord medicine (04.03.2017)
Published in The journal of spinal cord medicine (04.03.2017)
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Cerebral Infarction Associated with Accessory Middle Cerebral Arteries: Two Case Reports
Hiramatsu, Yu, Wakita, Masayuki, Matsuoka, Hideki, Kasuya, Jyunji, Hamada, Rikuzo, Takashima, Hiroshi
Published in Internal Medicine (01.01.2014)
Published in Internal Medicine (01.01.2014)
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Clinical diversity caused by novel IGHMBP2 variants
Yuan, Jun-Hui, Hashiguchi, Akihiro, Yoshimura, Akiko, Yaguchi, Hiroshi, Tsuzaki, Koji, Ikeda, Azusa, Wada-Isoe, Kenji, Ando, Masahiro, Nakamura, Tomonori, Higuchi, Yujiro, Hiramatsu, Yu, Okamoto, Yuji, Takashima, Hiroshi
Published in Journal of human genetics (01.06.2017)
Published in Journal of human genetics (01.06.2017)
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Novel heterozygous variants of SLC12A6 in Japanese families with Charcot–Marie–Tooth disease
Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui, Yoshimura, Akiko, Taniguchi, Takaki, Takei, Jun, Takeuchi, Mika, Hiramatsu, Yu, Shimizu, Fumitaka, Kubota, Masaya, Takeshima, Akari, Ueda, Takehiro, Koh, Kishin, Nagaoka, Utako, Tokashiki, Takashi, Sawai, Setsu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Sato, Ryota, Kanda, Takashi, Okamoto, Yuji, Takashima, Hiroshi
Published in Annals of clinical and translational neurology (01.07.2022)
Published in Annals of clinical and translational neurology (01.07.2022)
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Mitochondrial trifunctional protein deficiency: an adult patient with similar progress to Charcot-Marie-Tooth disease
Yamamoto, Yuki, Matsui, Naoko, Hiramatsu, Yu, Miyazaki, Yoshimichi, Nodera, Hiroyuki, Izumi, Yuishin, Takashima, Hiroshi, Kaji, Ryuji
Published in Rinsho Shinkeigaku (25.02.2017)
Published in Rinsho Shinkeigaku (25.02.2017)
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