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

Hiroyuki Ishiura

Showing results (1-10 of 236) with videos related to

Pageof 24
Sort By:
Rinsho Shinkeigaku = Clinical Neurology|June 26, 2025
[Molecular genetics of benign adult familial myoclonus epilepsy]Hiroyuki Ishiura
Brain and Nerve = Shinkei Kenkyu No Shinpo|May 12, 2025
[Genetics of Motor Neuron Diseases and Hereditary Spastic Paraplegia]Hiroyuki Ishiura
Rinsho Shinkeigaku = Clinical Neurology|February 13, 2015
[Molecular genetics and gene analysis of hereditary spastic paraplegia]Hiroyuki Ishiura
Journal of Neuromuscular Diseases|March 4, 2025
Recent progress in oculopharyngodistal myopathy research from clinical and genetic viewpointsHiroyuki Ishiura
Rinsho Shinkeigaku = Clinical Neurology|January 27, 2012
[Next-generation analysis on hereditary neurodegenerative disorders using next-generation sequencers]Hiroyuki Ishiura, Shoji Tsuji
Rinsho Shinkeigaku = Clinical Neurology|September 17, 2011
[Massively parallel sequence analysis for revealing causes of neuromuscular disorders]Hiroyuki Ishiura, Shoji Tsuji
Rinsho Shinkeigaku = Clinical Neurology|December 3, 2013
[Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is caused by a mutation in TFG]Hiroyuki Ishiura, Shoji Tsuji
Journal of Neurogenetics|November 6, 2015
Epidemiology and molecular mechanism of frontotemporal lobar degeneration/amyotrophic lateral sclerosis with repeat expansion mutation in C9orf72Hiroyuki Ishiura, Shoji Tsuji
Current Opinion in Genetics & Development|August 11, 2020
Advances in repeat expansion diseases and a new concept of repeat motif-phenotype correlationHiroyuki Ishiura, Shoji Tsuji
Journal of Human Genetics|January 20, 2023
Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP) spectrum disorderHiroyuki Ishiura, Shoji Tsuji, Tatsushi Toda
Pageof 24

Showing results (1-10 of 236) with videos related to

Sort By:
Pageof 24
Rinsho Shinkeigaku = Clinical Neurology|June 26, 2025
[Molecular genetics of benign adult familial myoclonus epilepsy]Hiroyuki Ishiura
Brain and Nerve = Shinkei Kenkyu No Shinpo|May 12, 2025
[Genetics of Motor Neuron Diseases and Hereditary Spastic Paraplegia]Hiroyuki Ishiura
Rinsho Shinkeigaku = Clinical Neurology|February 13, 2015
[Molecular genetics and gene analysis of hereditary spastic paraplegia]Hiroyuki Ishiura
Journal of Neuromuscular Diseases|March 4, 2025
Recent progress in oculopharyngodistal myopathy research from clinical and genetic viewpointsHiroyuki Ishiura
Rinsho Shinkeigaku = Clinical Neurology|January 27, 2012
[Next-generation analysis on hereditary neurodegenerative disorders using next-generation sequencers]Hiroyuki Ishiura, Shoji Tsuji
Rinsho Shinkeigaku = Clinical Neurology|September 17, 2011
[Massively parallel sequence analysis for revealing causes of neuromuscular disorders]Hiroyuki Ishiura, Shoji Tsuji
Rinsho Shinkeigaku = Clinical Neurology|December 3, 2013
[Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is caused by a mutation in TFG]Hiroyuki Ishiura, Shoji Tsuji
Journal of Neurogenetics|November 6, 2015
Epidemiology and molecular mechanism of frontotemporal lobar degeneration/amyotrophic lateral sclerosis with repeat expansion mutation in C9orf72Hiroyuki Ishiura, Shoji Tsuji
Current Opinion in Genetics & Development|August 11, 2020
Advances in repeat expansion diseases and a new concept of repeat motif-phenotype correlationHiroyuki Ishiura, Shoji Tsuji
Journal of Human Genetics|January 20, 2023
Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP) spectrum disorderHiroyuki Ishiura, Shoji Tsuji, Tatsushi Toda
Pageof 24