Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yasushi Oya

Showing results (31-40 of 95) with videos related to

Pageof 10
Sort By:
Neuromuscular Disorders : NMD|November 7, 2012
Respiratory dysfunction in patients severely affected by GNE myopathy (distal myopathy with rimmed vacuoles)Madoka Mori-Yoshimura, Yasushi Oya, Yukiko K Hayashi, et al.
Clinical Neurology and Neurosurgery|May 19, 2019
Chronic sarcoid myopathy mimicking sporadic inclusion body myositisMasayuki Miyazaki, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 13, 2013
Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy)Anna Cho, Yukiko K Hayashi, Kazunari Monma, et al.
Journal of the Neurological Sciences|March 16, 2020
Obstruction-related dysphagia in inclusion body myositis: Cricopharyngeal bar on videofluoroscopy indicates risk of aspirationKenichiro Taira, Toshiyuki Yamamoto, Madoka Mori-Yoshimura, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 5, 2014
[Beneficial effects of 3,4-diaminopyridine in a 26-year-old woman with DOK7 congenital myasthenic syndrome who was originally diagnosed with facioscapulohumeral dystrophy]Atsuko Nishikawa, Madoka Mori-Yoshimura, Tomoko Okamoto, et al.
BMJ Neurology Open|December 9, 2022
Long-term evaluation parameters in GNE myopathy: a 5-year observational follow-up natural history studyMadoka Mori-Yoshimura, Hiroyuki Yajima, Yasushi Oya, et al.
Environmental Health and Preventive Medicine|August 25, 2014
Three novel serum biomarkers, miR-1, miR-133a, and miR-206 for Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, and Becker muscular dystrophyYasunari Matsuzaka, Soichiro Kishi, Yoshitsugu Aoki, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 29, 2017
A case of chronic sarcoid myopathy with Basedow's disease and Sjogren's syndrome: A case series of sarcoid myopathyTakashi Isobe, Madoka Mori-Yoshimura, Yasushi Oya, et al.
Annals of Nuclear Medicine|August 29, 2013
Massive accumulation of 11C-Pittsburg compound B in the occipital lobes of a patient with early-onset dementia accompanied by muscle weakness and hypertonicityKimiteru Ito, Terunori Sano, Kouhei Kamiya, et al.
European Journal of Medical Genetics|April 28, 2026
COL12A1-related myopathic Ehlers-Danlos syndrome with Chiari I malformation: A clinical reportJun Shinmi, Hotake Takizawa, Yoshihiko Saito, et al.
Pageof 10

Showing results (31-40 of 95) with videos related to

Sort By:
Pageof 10
Neuromuscular Disorders : NMD|November 7, 2012
Respiratory dysfunction in patients severely affected by GNE myopathy (distal myopathy with rimmed vacuoles)Madoka Mori-Yoshimura, Yasushi Oya, Yukiko K Hayashi, et al.
Clinical Neurology and Neurosurgery|May 19, 2019
Chronic sarcoid myopathy mimicking sporadic inclusion body myositisMasayuki Miyazaki, Madoka Mori-Yoshimura, Toshiyuki Yamamoto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 13, 2013
Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy)Anna Cho, Yukiko K Hayashi, Kazunari Monma, et al.
Journal of the Neurological Sciences|March 16, 2020
Obstruction-related dysphagia in inclusion body myositis: Cricopharyngeal bar on videofluoroscopy indicates risk of aspirationKenichiro Taira, Toshiyuki Yamamoto, Madoka Mori-Yoshimura, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 5, 2014
[Beneficial effects of 3,4-diaminopyridine in a 26-year-old woman with DOK7 congenital myasthenic syndrome who was originally diagnosed with facioscapulohumeral dystrophy]Atsuko Nishikawa, Madoka Mori-Yoshimura, Tomoko Okamoto, et al.
BMJ Neurology Open|December 9, 2022
Long-term evaluation parameters in GNE myopathy: a 5-year observational follow-up natural history studyMadoka Mori-Yoshimura, Hiroyuki Yajima, Yasushi Oya, et al.
Environmental Health and Preventive Medicine|August 25, 2014
Three novel serum biomarkers, miR-1, miR-133a, and miR-206 for Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, and Becker muscular dystrophyYasunari Matsuzaka, Soichiro Kishi, Yoshitsugu Aoki, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 29, 2017
A case of chronic sarcoid myopathy with Basedow's disease and Sjogren's syndrome: A case series of sarcoid myopathyTakashi Isobe, Madoka Mori-Yoshimura, Yasushi Oya, et al.
Annals of Nuclear Medicine|August 29, 2013
Massive accumulation of 11C-Pittsburg compound B in the occipital lobes of a patient with early-onset dementia accompanied by muscle weakness and hypertonicityKimiteru Ito, Terunori Sano, Kouhei Kamiya, et al.
European Journal of Medical Genetics|April 28, 2026
COL12A1-related myopathic Ehlers-Danlos syndrome with Chiari I malformation: A clinical reportJun Shinmi, Hotake Takizawa, Yoshihiko Saito, et al.
Pageof 10