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

Hiroya Naruse

Showing results (1-10 of 32) with videos related to

Pageof 4
Sort By:
Neurocase|July 23, 2025
<i>VCP</i> p.Arg191Gln mutation in a patient with semantic dementia: a case reportRyota Kobayashi, Hiroya Naruse, Akihito Suzuki, et al.
Internal Medicine (Tokyo, Japan)|June 19, 2010
A case of osteoarthropathy due to Erdheim-Chester disease with overlapping Langerhans' cell infiltrationHiroya Naruse, Hirofumi Shoda, Akiko Okamoto, et al.
Rinsho Shinkeigaku = Clinical Neurology|October 30, 2015
[A patient with familial amyotrophic lateral sclerosis associated with a new valosin-containing protein (VCP) gene mutation]Mari Segawa, Akihiko Hoshi, Hiroya Naruse, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 15, 2025
An Autopsy Case of ALS Which Clinically Presented Sporadic Adult-Onset Lower Motor Neuron Disease and Genetically Had p. Leu127Ser (L126S) Variant in SOD1 and SMN2 DeletionKimiko Inoue, Harutoshi Fujimura, Kayo Ueda, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 2, 2020
Juvenile amyotrophic lateral sclerosis with complex phenotypes associated with novel <i>SYNE1</i> mutationsHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Neuropathology and Applied Neurobiology|July 10, 2026
Frontotemporal Lobar Degeneration-TDP Type C With Striatal Glial Cytoplasmic Inclusions and Motor Neuron DegenerationAkiko Uchino, Kazutomi Kanemaru, Airi Tarutani, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 3, 2013
Successful treatment of infliximab-associated immune-mediated sensory polyradiculopathy with intravenous immunoglobulinHiroya Naruse, Yu Nagashima, Risa Maekawa, et al.
Journal of the Peripheral Nervous System : JPNS|May 30, 2023
Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1Hiroya Naruse, So Okubo, Atsushi Sudo, et al.
Neurogenetics|March 9, 2019
Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populationsHiroya Naruse, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Auris, Nasus, Larynx|March 4, 2022
Clinical and electrophysiological findings of facial palsy in a case of hereditary gelsolin amyloidosisKaoru Yamakawa, Hironobu Nishijima, Akatsuki Kubota, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Neurocase|July 23, 2025
<i>VCP</i> p.Arg191Gln mutation in a patient with semantic dementia: a case reportRyota Kobayashi, Hiroya Naruse, Akihito Suzuki, et al.
Internal Medicine (Tokyo, Japan)|June 19, 2010
A case of osteoarthropathy due to Erdheim-Chester disease with overlapping Langerhans' cell infiltrationHiroya Naruse, Hirofumi Shoda, Akiko Okamoto, et al.
Rinsho Shinkeigaku = Clinical Neurology|October 30, 2015
[A patient with familial amyotrophic lateral sclerosis associated with a new valosin-containing protein (VCP) gene mutation]Mari Segawa, Akihiko Hoshi, Hiroya Naruse, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 15, 2025
An Autopsy Case of ALS Which Clinically Presented Sporadic Adult-Onset Lower Motor Neuron Disease and Genetically Had p. Leu127Ser (L126S) Variant in SOD1 and SMN2 DeletionKimiko Inoue, Harutoshi Fujimura, Kayo Ueda, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 2, 2020
Juvenile amyotrophic lateral sclerosis with complex phenotypes associated with novel <i>SYNE1</i> mutationsHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Neuropathology and Applied Neurobiology|July 10, 2026
Frontotemporal Lobar Degeneration-TDP Type C With Striatal Glial Cytoplasmic Inclusions and Motor Neuron DegenerationAkiko Uchino, Kazutomi Kanemaru, Airi Tarutani, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 3, 2013
Successful treatment of infliximab-associated immune-mediated sensory polyradiculopathy with intravenous immunoglobulinHiroya Naruse, Yu Nagashima, Risa Maekawa, et al.
Journal of the Peripheral Nervous System : JPNS|May 30, 2023
Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1Hiroya Naruse, So Okubo, Atsushi Sudo, et al.
Neurogenetics|March 9, 2019
Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populationsHiroya Naruse, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Auris, Nasus, Larynx|March 4, 2022
Clinical and electrophysiological findings of facial palsy in a case of hereditary gelsolin amyloidosisKaoru Yamakawa, Hironobu Nishijima, Akatsuki Kubota, et al.
Pageof 4