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Jun Mitsui

Showing results (111-120 of 163) with videos related to

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Acta Neuropathologica Communications|May 15, 2022
Clinical significance of NF2 alteration in grade I meningiomas revisited; prognostic impact integrated with extent of resection, tumour location, and Ki-67 indexYu Teranishi, Atsushi Okano, Satoru Miyawaki, et al.
Internal Medicine (Tokyo, Japan)|February 15, 2023
The Myocardial Accumulation of Aggregated Desmin Protein in a Case of Desminopathy with a de novo DES p.R406W MutationNaoki Takegami, Akihiko Mitsutake, Tatsuo Mano, et al.
Journal of Neurology|February 11, 2025
SOD1-related inherited peripheral neuropathies in a Japanese cohort: genetic variants and clinical insightsMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Annals of Clinical and Translational Neurology|April 28, 2022
Novel de novo POLR3B mutations responsible for demyelinating Charcot-Marie-Tooth disease in JapanMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Clinical Genetics|December 27, 2021
Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencingYumi Enomoto, Takayuki Yokoi, Yoshinori Tsurusaki, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 6, 2012
CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathyJun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Journal of the Neurological Sciences|October 1, 2025
Two Japanese families with adult-onset leukoencephalopathy caused by pathogenic variants in CST3Kenta Orimo, Takashi Matsukawa, Kazutaka Shiomi, et al.
Neurobiology of Aging|October 17, 2017
Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Parkinsonism & Related Disorders|December 12, 2018
Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletionYuta Ichinose, Hiroyuki Ishiura, Masaki Tanaka, et al.
Neurosurgery|May 15, 2025
Genetic Analysis of Intracranial Schwannomas: Differential NF2 Alteration Frequencies in Nonvestibular Schwannomas Versus Vestibular SchwannomasKenta Ohara, Satoru Miyawaki, Yu Teranishi, et al.
Pageof 17

Showing results (111-120 of 163) with videos related to

Sort By:
Pageof 17
Acta Neuropathologica Communications|May 15, 2022
Clinical significance of NF2 alteration in grade I meningiomas revisited; prognostic impact integrated with extent of resection, tumour location, and Ki-67 indexYu Teranishi, Atsushi Okano, Satoru Miyawaki, et al.
Internal Medicine (Tokyo, Japan)|February 15, 2023
The Myocardial Accumulation of Aggregated Desmin Protein in a Case of Desminopathy with a de novo DES p.R406W MutationNaoki Takegami, Akihiko Mitsutake, Tatsuo Mano, et al.
Journal of Neurology|February 11, 2025
SOD1-related inherited peripheral neuropathies in a Japanese cohort: genetic variants and clinical insightsMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Annals of Clinical and Translational Neurology|April 28, 2022
Novel de novo POLR3B mutations responsible for demyelinating Charcot-Marie-Tooth disease in JapanMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Clinical Genetics|December 27, 2021
Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencingYumi Enomoto, Takayuki Yokoi, Yoshinori Tsurusaki, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 6, 2012
CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathyJun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Journal of the Neurological Sciences|October 1, 2025
Two Japanese families with adult-onset leukoencephalopathy caused by pathogenic variants in CST3Kenta Orimo, Takashi Matsukawa, Kazutaka Shiomi, et al.
Neurobiology of Aging|October 17, 2017
Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Parkinsonism & Related Disorders|December 12, 2018
Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletionYuta Ichinose, Hiroyuki Ishiura, Masaki Tanaka, et al.
Neurosurgery|May 15, 2025
Genetic Analysis of Intracranial Schwannomas: Differential NF2 Alteration Frequencies in Nonvestibular Schwannomas Versus Vestibular SchwannomasKenta Ohara, Satoru Miyawaki, Yu Teranishi, et al.
Pageof 17