Ichizo Nishino - Dissemin

Papers authored by Ichizo Nishino

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2016 Keisuke Ikemoto, Shigeaki Suzuki, Akinori Uruha, Yurika Watanabe, Jin Nakahara, Ichizo Nishino

, Norihiro Suzuki

Enzyme-linked immunosorbent assays for diagnosis of immune-mediated necrotizing myopathy

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Ryuji Yajima

, Tetsuya Takahashi, Yo Higuchi, Masanori Ishikawa, Satomi Mitsuhashi, Ichizo Nishino

, Masatoyo Nishizawa

Japanese case of Emery-Dreifuss muscular dystrophy with a novelLMNAmissense mutation

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Kohei Hamanaka, Kanako Goto, Mami Arai, Koji Nagao, Chikashi Obuse, Satoru Noguchi, Yukiko K. Hayashi, Satomi Mitsuhashi, Ichizo Nishino

Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations

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Shinsuke Narumi, Tatsunori Natori, Haruna Miyazawa, Tadayoshi Kato, Hisashi Yonezawa, Ichizo Nishino

, Masayuki Nakamura, Akira Sano, Yasuo Terayama

Case of McLeod syndrome with a novel genetic mutation

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Wen-Chen Liang, Po-Ching Chou, Chia-Cheng Hung, Yi-Ning Su, Tsu-Min Kan, Wan-Zi Chen, Yukiko K. Hayashi, Ichizo Nishino

, Yuh-Jyh Jong

Probable high prevalence of limb-girdle muscular dystrophy type 2D in Taiwan

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Kohei Hamanaka, Ikuhiro Inami, Takahito Wada, Satomi Mitsuhashi, Satoru Noguchi, Yukiko K. Hayashi, Ichizo Nishino

Muscle from a 20-week-old myotubular myopathy fetus is not myotubular

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Mariko Okubo, Narihiro Minami, Kanako Goto, Yuichi Goto, Satoru Noguchi, Satomi Mitsuhashi, Ichizo Nishino

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations

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Atsuko Nishikawa, Madoka Mori-Yoshimura, Kazuhiko Segawa, Yukiko K. Hayashi, Toshiaki Takahashi, Yuko Saito, Ikuya Nonaka, Martin Krahn, Nicolas Levy, Jun Shimizu, Jun Mitsui, En Kimura, Jun Goto, Naohiro Yonemoto, Masashi Aoki and 3 other authors

Respiratory and cardiac function in japanese patients with dysferlinopathy

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Yukio Mizuno, Madoka Mori-Yoshimura, Tomoko Okamoto, Yasushi Oya, Ichizo Nishino

, Miho Murata

Two cases of sporadic late onset nemaline myopathy effectively treated with immunotherapy

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2015 Akinori Uruha, Satoru Noguchi, Yukiko K. Hayashi, Rie S. Tsuburaya, Takahiro Yonekawa, Ikuya Nonaka, Ichizo Nishino

Hepatitis C virus infection in inclusion body myositis

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Koya Kawase, Ichizo Nishino

, Mari Sugimoto, Takao Togawa, Tokio Sugiura, Masanori Kouwaki, Tetsuya Kibe, Norihisa Koyama, Kenji Yokochi

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state

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Yimeng Zhao, Haruo Ogawa, Shin-Ichiro Yonekura, Hiroaki Mitsuhashi, Satomi Mitsuhashi, Ichizo Nishino

, Chikashi Toyoshima, Shoichi Ishiura

Functional analysis of SERCA1b, a highly expressed SERCA1 variant in myotonic dystrophy type 1 muscle

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This paper is made freely available by the publisher.

Wen-Chen Liang, Wenhua Zhu, Satomi Mitsuhashi, Satoru Noguchi, Michael Sacher, Megumu Ogawa, Hsiang-Hung Shih, Yuh-Jyh Jong, Ichizo Nishino

Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations: broadening of the phenotype

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Jantima Tanboon, Sorawit Viravan, Yukiko K. Hayashi, Ichizo Nishino

, Tumtip Sangruchi

2 Month-Old Male with Hypotonia

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Hesham Montassir, Yoshihiro Maegaki, Kei Murayama, Taro Yamazaki, Masakazu Kohda, Akira Ohtake, Hiroyasu Iwasa, Yukiko Yatsuka, Yasushi Okazaki, Chitose Sugiura, Ikuo Nagata, Mitsuo Toyoshima, Yoshiaki Saito

, Masayuki Itoh, Ichizo Nishino

and 1 other authors

Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological report

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Tetsuya Oda, Hui Xiong, Kazuhiro Kobayashi, Shuo Wang, Wataru Satake, Hui Jiao, Yanling Yang, Pei-Chieng Cha

, Yukiko K. Hayashi, Ichizo Nishino

, Yutaka Suzuki, Sumio Sugano, Xiru Wu, Tatsushi Toda

A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy

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Akinori Uruha, Satoru Noguchi, Wakiro Sato, Hiroaki Nishimura, Satomi Mitsuhashi, Takashi Yamamura, Ichizo Nishino

Plasma IP-10 level distinguishes inflammatory myopathy

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Akiko Furuta, Hisae Kikuchi, Hiromi Fujita, Daisuke Yamada, Yuuki Fujiwara, Tomohiro Kabuta, Ichizo Nishino

, Keiji Wada, Yasuo Uchiyama

Property of Lysosomal Storage Disease Associated with Midbrain Pathology in the Central Nervous System of Lamp-2–Deficient Mice

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Shigeaki Suzuki, Atsuko Nishikawa, Masataka Kuwana, Hiroaki Nishimura, Yurika Watanabe, Jin Nakahara, Yukiko K. Hayashi, Norihiro Suzuki, Ichizo Nishino

Inflammatory myopathy with anti-signal recognition particle antibodies: case series of 100 patients

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Oranee Sanmaneechai, Surachai Likasitwattanakul, Tumtip Sangruchi, Ichizo Nishino

Ophthalmoplegia in congenital neuromuscular disease with uniform type 1 fiber

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Papers authored by Ichizo Nishino