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 (41-50 of 95) with videos related to

Pageof 10
Sort By:
Rinsho Shinkeigaku = Clinical Neurology|October 22, 2010
[Limb-girdle muscular dystrophy type 2M with adult-onset loss of ambulation. A case report]Yoshiyuki Kondo, Madoka Mori-Yoshimura, Yukiko K Hayashi, et al.
European Heart Journal. Case Reports|June 16, 2023
Sick sinus syndrome concomitant with myopathy associated with anti-mitochondrial antibodies: a case reportMaya Ishiguro, Yuji Nagatomo, Kanki Inoue, et al.
Journal of the Neurological Sciences|March 31, 2004
FSHD-like patients without 4q35 deletionGaku Yamanaka, Kanako Goto, Tadayuki Ishihara, et al.
Plos One|December 16, 2016
Characterization and Functional Analysis of Extracellular Vesicles and Muscle-Abundant miRNAs (miR-1, miR-133a, and miR-206) in C2C12 Myocytes and mdx MiceYasunari Matsuzaka, Jun Tanihata, Hirofumi Komaki, et al.
Journal of Neuromuscular Diseases|July 12, 2020
Respiratory Dysfunction in Becker Muscular Dystrophy Patients: A Case Series and Autopsy ReportMadoka Mori-Yoshimura, Yasushi Oya, Hirohumi Komaki, et al.
Muscle & Nerve|August 9, 2016
Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2AMadoka Mori-Yoshimura, Kazuhiko Segawa, Narihiro Minami, et al.
Journal of Neuromuscular Diseases|February 22, 2020
Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature ReviewTomoya Taminato, Madoka Mori-Yoshimura, Jun Miki, et al.
Neuromuscular Disorders : NMD|June 16, 2022
A 78-year-old Japanese male with late-onset PHKA1-associated distal myopathy: Case report and literature reviewMadoka Mori-Yoshimura, Kazutaka Aizawa, Yasushi Oya, et al.
Brain & Development|March 9, 2019
Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutationChihiro Matsumoto, Madoka Mori-Yoshimura, Satoru Noguchi, et al.
Annals of Clinical and Translational Neurology|November 19, 2025
Chronological and Spatial Distribution of Skeletal Muscle Fat Replacement in FHL1-Related MyopathiesRui Shimazaki, Satoru Noguchi, Hotake Takizawa, et al.
Pageof 10

Showing results (41-50 of 95) with videos related to

Sort By:
Pageof 10
Rinsho Shinkeigaku = Clinical Neurology|October 22, 2010
[Limb-girdle muscular dystrophy type 2M with adult-onset loss of ambulation. A case report]Yoshiyuki Kondo, Madoka Mori-Yoshimura, Yukiko K Hayashi, et al.
European Heart Journal. Case Reports|June 16, 2023
Sick sinus syndrome concomitant with myopathy associated with anti-mitochondrial antibodies: a case reportMaya Ishiguro, Yuji Nagatomo, Kanki Inoue, et al.
Journal of the Neurological Sciences|March 31, 2004
FSHD-like patients without 4q35 deletionGaku Yamanaka, Kanako Goto, Tadayuki Ishihara, et al.
Plos One|December 16, 2016
Characterization and Functional Analysis of Extracellular Vesicles and Muscle-Abundant miRNAs (miR-1, miR-133a, and miR-206) in C2C12 Myocytes and mdx MiceYasunari Matsuzaka, Jun Tanihata, Hirofumi Komaki, et al.
Journal of Neuromuscular Diseases|July 12, 2020
Respiratory Dysfunction in Becker Muscular Dystrophy Patients: A Case Series and Autopsy ReportMadoka Mori-Yoshimura, Yasushi Oya, Hirohumi Komaki, et al.
Muscle & Nerve|August 9, 2016
Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2AMadoka Mori-Yoshimura, Kazuhiko Segawa, Narihiro Minami, et al.
Journal of Neuromuscular Diseases|February 22, 2020
Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature ReviewTomoya Taminato, Madoka Mori-Yoshimura, Jun Miki, et al.
Neuromuscular Disorders : NMD|June 16, 2022
A 78-year-old Japanese male with late-onset PHKA1-associated distal myopathy: Case report and literature reviewMadoka Mori-Yoshimura, Kazutaka Aizawa, Yasushi Oya, et al.
Brain & Development|March 9, 2019
Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutationChihiro Matsumoto, Madoka Mori-Yoshimura, Satoru Noguchi, et al.
Annals of Clinical and Translational Neurology|November 19, 2025
Chronological and Spatial Distribution of Skeletal Muscle Fat Replacement in FHL1-Related MyopathiesRui Shimazaki, Satoru Noguchi, Hotake Takizawa, et al.
Pageof 10