Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kana Yatabe"'
Autor:
Narihiro Minami, Madoka Mori-Yoshimura, Hotake Takizawa, Ichizo Nishino, Yoshitsugu Aoki, Yuji Takahashi, Kenichiro Taira, Yasumasa Hashimoto, Kana Yatabe, Nobuyuki Murakami
Publikováno v:
Neuromuscular Disorders. 31:666-672
Duchenne and Becker muscular dystrophy (DMD/BMD) are commonly inherited muscle disorders. We report a 31-year-old male who had muscle symptoms with left-right differences and intellectual disability. He was diagnosed with BMD at age 15 primarily base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6d9aa413ad3a30451d277baaa81c5e0
https://doi.org/10.1016/j.nmd.2021.04.006
https://doi.org/10.1016/j.nmd.2021.04.006
Autor:
Eriko Koshimizu, Satomi Mitsuhashi, Masaaki Shiina, Ikuya Nonaka, Satoshi Kuru, Takeshi Mizuguchi, Mikiya Suzuki, Hirotomo Saitsu, Naomichi Matsumoto, Noriko Miyake, Yukiko K. Hayashi, Ichizo Nishino, Satoko Miyatake, Yuzo Tanaka, Yoshinori Tsurusaki, Mitsuko Nakashima, Atsuko Nishikawa, Jeffrey A. Towbin, Mitsuru Kawai, Enkhsaikhan Purevjav, Kazuhiro Ogata, Kana Yatabe, Katsuhisa Ogata
Publikováno v:
The American Journal of Human Genetics. 100:169-178
Nemaline myopathy (NM) is a common form of congenital nondystrophic skeletal muscle disease characterized by muscular weakness of proximal dominance, hypotonia, and respiratory insufficiency but typically not cardiac dysfunction. Wide variation in se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daaf3705934b2771a09649e931763406
https://doi.org/10.1016/j.ajhg.2016.11.017
https://doi.org/10.1016/j.ajhg.2016.11.017
Publikováno v:
Neuromuscular Disorders. 30:S147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ee32df659c038211d9aa944be5f1127
https://doi.org/10.1016/j.nmd.2020.08.342
https://doi.org/10.1016/j.nmd.2020.08.342
Autor:
Satoko Miyatake, Masashi Suzuki, Katsuhisa Ogata, Satomi Mitsuhashi, Satoshi Kuru, Kana Yatabe, Atsuko Nishikawa, Ikuya Nonaka, Ichizo Nishino, Yuichi Hayashi, Y. Tanaka, Naomichi Matsumoto
Publikováno v:
Journal of the Neurological Sciences. 381:58-59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::962c91c37be691e4a6f8d6ab131404e6
https://doi.org/10.1016/j.jns.2017.08.224
https://doi.org/10.1016/j.jns.2017.08.224
Autor:
Katsuhisa Ogata, Hitoshi Mochizuki, Toshiki Shigeyama, Kana Yatabe, Takuhisa Tamura, Mikiya Suzuki, Satoko Miyatake, Mitsuru Kawai
Publikováno v:
Internal Medicine. 47:1207-1210
Objective This study investigated the relationship between mental retardation and lifetime events in patients with Duchenne muscular dystrophy (DMD). Methods The data on mental retardation and ages of lifetime events (first walking, loss of ambulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9980c835d346b4b943d8ab665bcf237d
https://doi.org/10.2169/internalmedicine.47.0907
https://doi.org/10.2169/internalmedicine.47.0907
Autor:
Kiyoshi Ishikawa, Kyoko Maruta, Shigehiro Imamura, Masaaki Konagaya, Hiroo Watanabe, Takashi Nakajima, Hirofumi Komaki, Yasuko Tokita, Toshio Saito, Satoko Takanoha, Kenji Kuroda, Tetsuro Konishi, Shigeo Mamiya, Rie Shimazaki, Kana Yatabe, Susumu Shinno, Masayuki Sasaki, Katsunori Tatara, Tomoko Mizuno, M. Yoshioka, Kiyokaku Kon, Tadayuki Ishihara, Takashi Mikata, Maki Mitani, Kiyotaka Fukuda
Publikováno v:
Braindevelopment. 34(9)
Although muscular dystrophy patients often have feeding difficulty and need long-term enteral nutrition, only a few reports have described gastrostomy feeding in these patients. This study was designed to evaluate the efficacy and tolerance of gastro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::830594a6336ab68e9840aff39cbe1e0e
https://pubmed.ncbi.nlm.nih.gov/22204944
https://pubmed.ncbi.nlm.nih.gov/22204944
Autor:
Mitsuru Kawai, Kana Yatabe
Publikováno v:
Journal of neurology. 244(8)
Ulex europaeus agglutinin I (UEA I) binding was studied in 83 patients with various neuromuscular disorders. UEA I labelled endomysial capillaries and endothelial cells of perimysial blood vessels in all the examined muscles. There was no UEA I bindi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::319b050ec3613f9185836bcda037f253
https://pubmed.ncbi.nlm.nih.gov/9309554
https://pubmed.ncbi.nlm.nih.gov/9309554
Autor:
Masashi Suzuki, Ikuya Nonaka, K. Momma, R. Akatani, Yutaka Honma, Y. Tanaka, T. Shigeyama, T. Tamura, Katsuhisa Ogata, Kana Yatabe, Mitsuru Kawai
Publikováno v:
Journal of the Neurological Sciences. 333:e446
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473b1b4186308b7a802193b8bd3d5ac0
https://doi.org/10.1016/j.jns.2013.07.1596
https://doi.org/10.1016/j.jns.2013.07.1596
Autor:
T. Shigeyama, Kana Yatabe, A. Noju, Yutaka Honma, M. Takata, Mitsuru Kawai, Katsuhisa Ogata, K. Nagata, Ikuya Nonaka, Mikiya Suzuki, K. Momma, Takuhisa Tamura, Yuzo Tanaka
Publikováno v:
Neuromuscular Disorders. 22:900
Myotonic dystrophy (DM) is an autosomal dominant disorder with dysfunction of multiple systems. Concurrent features of skeletal muscles, myotonia and weakness, do not make difficulties with DM patients in early and mild stage, and progress slowly. Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9a03c6c87cb47aca1dc1ee0b57eef84
https://doi.org/10.1016/j.nmd.2012.06.318
https://doi.org/10.1016/j.nmd.2012.06.318