Search research articles
Contact Us
Filters
Showing results (51-60 of 95) with videos related to
Page
of 10
Sort By:
Journal of Human Genetics
|
January 17, 2014
Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2
Takahiro Nakayama, Harumasa Nakamura, Yasushi Oya, et al.
Brain & Development
|
April 17, 2010
Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection
Sae Hanai, Hirofumi Komaki, Hiroshi Sakuma, et al.
Medicine
|
October 20, 2017
Cardiac conduction disturbances and aging in patients with Duchenne muscular dystrophy
Kazuhiko Segawa, Hirofumi Komaki, Madoka Mori-Yoshimura, et al.
Journal of Neurology
|
September 27, 2020
Cricopharyngeal bar on videofluoroscopy: high specificity for inclusion body myositis
Kenichiro 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 report
Ryouhei 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 Study
Rui 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 cardiomyopathy
Takuro 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 pathology
Rie 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 myopathy
Atsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Neuromuscular Disorders : NMD
|
March 25, 2014
GNE myopathy: a prospective natural history study of disease progression
Madoka Mori-Yoshimura, Yasushi Oya, Hiroyuki Yajima, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 95) with videos related to
Sort By:
Page
of 10
Journal of Human Genetics
|
January 17, 2014
Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2
Takahiro Nakayama, Harumasa Nakamura, Yasushi Oya, et al.
Brain & Development
|
April 17, 2010
Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection
Sae Hanai, Hirofumi Komaki, Hiroshi Sakuma, et al.
Medicine
|
October 20, 2017
Cardiac conduction disturbances and aging in patients with Duchenne muscular dystrophy
Kazuhiko Segawa, Hirofumi Komaki, Madoka Mori-Yoshimura, et al.
Journal of Neurology
|
September 27, 2020
Cricopharyngeal bar on videofluoroscopy: high specificity for inclusion body myositis
Kenichiro 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 report
Ryouhei 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 Study
Rui 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 cardiomyopathy
Takuro 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 pathology
Rie 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 myopathy
Atsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Neuromuscular Disorders : NMD
|
March 25, 2014
GNE myopathy: a prospective natural history study of disease progression
Madoka Mori-Yoshimura, Yasushi Oya, Hiroyuki Yajima, et al.
Page
of 10