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

Yujiro Higuchi

Showing results (111-120 of 154) with videos related to

Pageof 16
Sort By:
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|April 3, 2026
Arginine ameliorates motor and survival deficits in MFN2-Deficient Drosophila modelsMasahiro Ando, Yuji Okamoto, Yujiro Higuchi, et al.
Acta Neuropathologica Communications|August 23, 2024
Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implicationsTakahiro Hobara, Yujiro Higuchi, Mari Yoshida, et al.
Journal of Human Genetics|February 17, 2017
Clinical diversity caused by novel IGHMBP2 variantsJun-Hui Yuan, Akihiro Hashiguchi, Akiko Yoshimura, et al.
Cerebellum (London, England)|September 9, 2021
Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in JapanYujiro Higuchi, Masahiro Ando, Akiko Yoshimura, et al.
Neurology. Genetics|October 30, 2025
Frameshift and Copy Number Variants in <i>SACS</i>-Related NeuropathyJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Journal of Neurology|June 29, 2026
Genetic spectrum and clinical features of PMP22 point mutations in Japanese Charcot-Marie-Tooth diseaseChikashi Yano, Masahiro Ando, Yujiro Higuchi, et al.
Annals of Clinical and Translational Neurology|October 1, 2025
Nationwide Characterization of MFN2-Related CMT in 176 Japanese Patients: Clinical and Genetic InsightsMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Brain & Development|September 19, 2015
A mild case of giant axonal neuropathy without central nervous system manifestationReiko Koichihara, Takashi Saito, Akihiko Ishiyama, et al.
Orphanet Journal of Rare Diseases|April 2, 2026
Six novel SACS mutations expand the autosomal recessive spastic ataxia of Charlevoix-Saguenay spectrumSusumu Ikenoshita, Toshiya Nomura, Haruo Shimazaki, et al.
Journal of Neurology|August 13, 2025
Systemic mitochondrial involvement in mitochondrial myopathy with episodic hyper-creatine kinase-emia: insights from an autopsy caseRisa Nagatomo, Yu Hiramatsu, Yusuke Sakiyama, et al.
Pageof 16

Showing results (111-120 of 154) with videos related to

Sort By:
Pageof 16
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|April 3, 2026
Arginine ameliorates motor and survival deficits in MFN2-Deficient Drosophila modelsMasahiro Ando, Yuji Okamoto, Yujiro Higuchi, et al.
Acta Neuropathologica Communications|August 23, 2024
Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implicationsTakahiro Hobara, Yujiro Higuchi, Mari Yoshida, et al.
Journal of Human Genetics|February 17, 2017
Clinical diversity caused by novel IGHMBP2 variantsJun-Hui Yuan, Akihiro Hashiguchi, Akiko Yoshimura, et al.
Cerebellum (London, England)|September 9, 2021
Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in JapanYujiro Higuchi, Masahiro Ando, Akiko Yoshimura, et al.
Neurology. Genetics|October 30, 2025
Frameshift and Copy Number Variants in <i>SACS</i>-Related NeuropathyJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Journal of Neurology|June 29, 2026
Genetic spectrum and clinical features of PMP22 point mutations in Japanese Charcot-Marie-Tooth diseaseChikashi Yano, Masahiro Ando, Yujiro Higuchi, et al.
Annals of Clinical and Translational Neurology|October 1, 2025
Nationwide Characterization of MFN2-Related CMT in 176 Japanese Patients: Clinical and Genetic InsightsMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Brain & Development|September 19, 2015
A mild case of giant axonal neuropathy without central nervous system manifestationReiko Koichihara, Takashi Saito, Akihiko Ishiyama, et al.
Orphanet Journal of Rare Diseases|April 2, 2026
Six novel SACS mutations expand the autosomal recessive spastic ataxia of Charlevoix-Saguenay spectrumSusumu Ikenoshita, Toshiya Nomura, Haruo Shimazaki, et al.
Journal of Neurology|August 13, 2025
Systemic mitochondrial involvement in mitochondrial myopathy with episodic hyper-creatine kinase-emia: insights from an autopsy caseRisa Nagatomo, Yu Hiramatsu, Yusuke Sakiyama, et al.
Pageof 16