Female dystrophinopathy: Review of current literature von Ishizaki, Masatoshi, Kobayashi, Michio, Adachi, Katsuhito, Matsumura, Tsuyoshi, Kimura, En

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Detection and management of cardiomyopathy in female dystrophinopathy carriers von Adachi, Katsuhito, Hashiguchi, Shuji, Saito, Miho, Kashiwagi, Setsuko, Miyazaki, Tatsushi, Kawai, Hisaomi, Yamada, Hirotsugu, Iwase, Takashi, Akaike, Masashi, Takao, Shoichiro, Kobayashi, Michio, Ishizaki, Masatoshi, Matsumura, Tuyoshi, Mori-Yoshimura, Madoka, Kimura, En

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Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan von Kobayashi, Michio, Hatakeyama, Tomoyuki, Ishizaki, Masatoshi, Adachi, Katsuhito, Morita, Mizuki, Yonemoto, Naohiro, Matsumura, Tsuyoshi, Toyoshima, Itaru, Kimura, En

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Voltage-gated potassium channel complex antibodies in Creutzfeldt-Jakob disease von Fujita, Koji, Yuasa, Tatsuhiko, Watanabe, Osamu, Takahashi, Yukitoshi, Hashiguchi, Shuji, Adachi, Katsuhito, Izumi, Yuishin, Kaji, Ryuji

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Prolonged apnea/hypopnea during water swallowing in patients with amyotrophic lateral sclerosis von Nozaki, Sonoko, Sugishita, Shuhei, Saito, Toshio, Umaki, Yoshifumi, Adachi, Katsuhito, Shinno, Susumu

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Voltage-gated potassium channel complex antibodies in Creutzfeldt-Jakob disease von Fujita, Koji, Yuasa, Tatsuhiko, Watanabe, Osamu, Takahashi, Yukitoshi, Hashiguchi, Shuji, Adachi, Katsuhito, Izumi, Yuishin, Kaji, Ryuji

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Survey on genetic counseling and health management for symptomatic and asymptomatic female dystrophinopathy carriers in Japan today von Kobayashi, Michio, Ishizaki, Masatoshi, Adachi, Katsuhito, Yonemoto, Naohiro, Matsumura, Tsuyoshi, Toyoshima, Itaru, Kimura, En

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Detection of anti-glutamate receptor [epsi]2 and anti-N-methyl-d-aspartate receptor antibodies in a patient with sporadic Creutzfeldt-Jakob disease von Fujita, Koji, Yuasa, Tatsuhiko, Takahashi, Yukitoshi, Tanaka, Keiko, Hashiguchi, Shuji, Adachi, Katsuhito, Izumi, Yuishin, Kaji, Ryuji

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Detection of anti-glutamate receptor ε2 and anti-N-methyl-d-aspartate receptor antibodies in a patient with sporadic Creutzfeldt–Jakob disease von Fujita, Koji, Yuasa, Tatsuhiko, Takahashi, Yukitoshi, Tanaka, Keiko, Hashiguchi, Shuji, Adachi, Katsuhito, Izumi, Yuishin, Kaji, Ryuji

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Disorders of Skeletal and Cardiac Muscle, and Central Nervous System in Female Gene Carriers of Duchenne Muscular Dystrophy von ADACHI, Katsuhito

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Different manners of sarcoglycan expression in genetically proven α-sarcoglycan deficiency and γ-sarcoglycan deficiency von HIGUCHI, I, KAWAI, H, UMAKI, Y, KAWAJIRI, M, ADACHI, K, FUKUNAGA, H, NAKAGAWA, M, ARIMURA, K, OSAME, M

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Second Opinion Clinic in Tokushima National Hospital for Neuro-Muscular Diseases von ADACHI, Katsuhito, KAWAI, Hisaomi

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Proteolysis of β-dystroglycan in muscular diseases von Matsumura, Kiichiro, Zhong, Di, Saito, Fumiaki, Arai, Ken, Adachi, Katsuhito, Kawai, Hisaomi, Higuchi, Itsuro, Nishino, Ichizo, Shimizu, Teruo

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Plasma Levels of Brain Natriuretic Peptide as an Index for Evaluation of Cardiac Function in Female Gene Carriers of Duchenne Muscular Dystrophy von ADACHI, Katsuhito, KAWAI, Hisaomi, SAITO, Miho, NARUO, Takako, KIMURA, Chiyomi, MINE, Hideki, INUI, Toshio, KASHIWAGI, Setsuko, AKAIKE, Masashi

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Cardiac dysfunction with Becker muscular dystrophy von Saito, Miho, Kawai, Hisaomi, Akaike, Masashi, Adachi, Katsuhito, Nishida, Yoshihito, Saito, Shiro

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Is an oral disintegrating tablets a formulation that is easy to ingest for patients experiencing difficulty with eating and swallowing? von Umaki, Yoshifumi, Nozaki, Sonoko, Sugishita, Shuhei, Shiimoto, Kumiko, Hashiguchi, Shuji, Inui, Toshio, Adachi, Katsuhito

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ジストロフィン異常症保因者の遺伝カウンセリング・健康管理の実態に関する調査 von 小林, 道雄, 石崎, 雅俊, 足立, 克仁, 米本, 直裕, 松村, 剛, 豊島, 至, 木村, 円

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Diagnostic utility of cardiac magnetic resonance for detection of cardiac involvement in female carriers of Duchenne muscular dystrophy von Iwase, Takashi, Takao, Shoichiro, Akaike, Masashi, Adachi, Katsuhito, Sumitomo-Ueda, Yuka, Yagi, Shusuke, Niki, Toshiyuki, Kusunose, Kenya, Tomita, Noriko, Hirata, Yoichiro, Yamaguchi, Koji, Koshiba, Kunihiko, Taketani, Yoshio, Yamada, Hirotsugu, Soeki, Takeshi, Wakatsuki, Tetsuzo, Aihara, Ken-ichi, Harada, Masafumi, Nishitani, Hiromu, Sata, Masataka

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Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families von Kawai, Hisaomi, Akaike, Masashi, Kunishige, Makoto, Inui, Toshio, Adachi, Katsuhito, Kimura, Chiyomi, Kawajiri, Masakazu, Nishida, Yoshihiko, Endo, Itsuro, Kashiwagi, Setsuko, Nishino, Hiroshi, Fujiwara, Tsutomu, Okuno, Shiro, Roudaut, Carinne, Richard, Isabelle, Beckmann, Jacques S., Miyoshi, Kazuo, Matsumoto, Toshio

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Is an oral disintegrating tablets a formulation that is easy to ingest for patients experiencing difficulty with eating and swallowing? von Umaki, Yoshifumi, Nozaki, Sonoko, Sugishita, Shuhei, Shiimoto, Kumiko, Hashiguchi, Shuji, Inui, Toshio, Adachi, Katsuhito

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