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Yasushi Oya

Showing results (51-60 of 95) with videos related to

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Journal of Human Genetics|January 17, 2014
Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2Takahiro Nakayama, Harumasa Nakamura, Yasushi Oya, et al.
Brain & Development|April 17, 2010
Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infectionSae Hanai, Hirofumi Komaki, Hiroshi Sakuma, et al.
Medicine|October 20, 2017
Cardiac conduction disturbances and aging in patients with Duchenne muscular dystrophyKazuhiko Segawa, Hirofumi Komaki, Madoka Mori-Yoshimura, et al.
Journal of Neurology|September 27, 2020
Cricopharyngeal bar on videofluoroscopy: high specificity for inclusion body myositisKenichiro Taira, Toshiyuki Yamamoto, Madoka Mori-Yoshimura, et al.
Journal of Human Genetics|June 7, 2020
Severe cardiac involvement with preserved truncated dystrophin expression in Becker muscular dystrophy by +1G>A DMD splice-site mutation: a case reportRyouhei Komaki, Yasumasa Hashimoto, Madoka Mori-Yoshimura, et al.
Muscle & Nerve|April 14, 2026
Spatiotemporal Patterns of Fat Replacement in SELENON-Related Myopathy: A Whole-Body Imaging StudyRui Shimazaki, Satoru Noguchi, Wakako Yoshioka, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|November 19, 2008
Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathyTakuro Arimura, Yukiko K Hayashi, Terumi Murakami, et al.
Neuromuscular Disorders : NMD|December 27, 2011
Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathologyRie S Tsuburaya, Kazunari Monma, Yasushi Oya, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Neuromuscular Disorders : NMD|March 25, 2014
GNE myopathy: a prospective natural history study of disease progressionMadoka Mori-Yoshimura, Yasushi Oya, Hiroyuki Yajima, et al.
Pageof 10

Showing results (51-60 of 95) with videos related to

Sort By:
Pageof 10
Journal of Human Genetics|January 17, 2014
Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2Takahiro Nakayama, Harumasa Nakamura, Yasushi Oya, et al.
Brain & Development|April 17, 2010
Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infectionSae Hanai, Hirofumi Komaki, Hiroshi Sakuma, et al.
Medicine|October 20, 2017
Cardiac conduction disturbances and aging in patients with Duchenne muscular dystrophyKazuhiko Segawa, Hirofumi Komaki, Madoka Mori-Yoshimura, et al.
Journal of Neurology|September 27, 2020
Cricopharyngeal bar on videofluoroscopy: high specificity for inclusion body myositisKenichiro Taira, Toshiyuki Yamamoto, Madoka Mori-Yoshimura, et al.
Journal of Human Genetics|June 7, 2020
Severe cardiac involvement with preserved truncated dystrophin expression in Becker muscular dystrophy by +1G>A DMD splice-site mutation: a case reportRyouhei Komaki, Yasumasa Hashimoto, Madoka Mori-Yoshimura, et al.
Muscle & Nerve|April 14, 2026
Spatiotemporal Patterns of Fat Replacement in SELENON-Related Myopathy: A Whole-Body Imaging StudyRui Shimazaki, Satoru Noguchi, Wakako Yoshioka, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|November 19, 2008
Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathyTakuro Arimura, Yukiko K Hayashi, Terumi Murakami, et al.
Neuromuscular Disorders : NMD|December 27, 2011
Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathologyRie S Tsuburaya, Kazunari Monma, Yasushi Oya, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Neuromuscular Disorders : NMD|March 25, 2014
GNE myopathy: a prospective natural history study of disease progressionMadoka Mori-Yoshimura, Yasushi Oya, Hiroyuki Yajima, et al.
Pageof 10