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Jun Mitsui

Showing results (121-130 of 163) with videos related to

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Journal of the Neurological Sciences|April 8, 2025
Clinical, neuroimaging and genetic findings in the Japanese case series of CLCN2-related leukoencephalopathyKenta Orimo, Takashi Matsukawa, Akihiko Mitsutake, et al.
Biomedicines|July 27, 2022
Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis PossibleMasahiro Ando, Yujiro Higuchi, Junhui Yuan, et al.
Scientific Reports|July 21, 2020
Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosisHiroki Hongo, Satoru Miyawaki, Hideaki Imai, et al.
Acta Neuropathologica Communications|September 26, 2023
Meningiomas in patients with neurofibromatosis type 2 predominantly comprise 'immunogenic subtype' tumours characterised by macrophage infiltrationYu Teranishi, Satoru Miyawaki, Masahiro Nakatochi, et al.
Muscle & Nerve|June 20, 2015
Respiratory and cardiac function in japanese patients with dysferlinopathyAtsuko Nishikawa, Madoka Mori-Yoshimura, Kazuhiko Segawa, et al.
European Journal of Human Genetics : EJHG|February 12, 2026
Delineating the Genetic Basis of RNF213-related vasculopathies: The association of PKHD1 variants with bilateral cerebral vasculopathyDaiichiro Ishigami, Shinichi Namba, Satoru Miyawaki, et al.
Journal of Human Genetics|January 14, 2022
Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatmentsTakaki Taniguchi, Masahiro Ando, Yuji Okamoto, et al.
Neurology|January 28, 2014
Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in JapanMegumi Yamada, Masaki Tanaka, Mari Takagi, et al.
Journal of Human Genetics|January 29, 2022
An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese familiesMasahiro Ando, Yujiro Higuchi, Yuji Okamoto, et al.
Scientific Reports|October 10, 2025
RNF213 c.14429G > A (p.Arg4810Lys) is associated with non-arteritic retinal artery occlusionDaisuke Shimada, Satoru Miyawaki, Kaoru Nakanishi, et al.
Pageof 17

Showing results (121-130 of 163) with videos related to

Sort By:
Pageof 17
Journal of the Neurological Sciences|April 8, 2025
Clinical, neuroimaging and genetic findings in the Japanese case series of CLCN2-related leukoencephalopathyKenta Orimo, Takashi Matsukawa, Akihiko Mitsutake, et al.
Biomedicines|July 27, 2022
Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis PossibleMasahiro Ando, Yujiro Higuchi, Junhui Yuan, et al.
Scientific Reports|July 21, 2020
Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosisHiroki Hongo, Satoru Miyawaki, Hideaki Imai, et al.
Acta Neuropathologica Communications|September 26, 2023
Meningiomas in patients with neurofibromatosis type 2 predominantly comprise 'immunogenic subtype' tumours characterised by macrophage infiltrationYu Teranishi, Satoru Miyawaki, Masahiro Nakatochi, et al.
Muscle & Nerve|June 20, 2015
Respiratory and cardiac function in japanese patients with dysferlinopathyAtsuko Nishikawa, Madoka Mori-Yoshimura, Kazuhiko Segawa, et al.
European Journal of Human Genetics : EJHG|February 12, 2026
Delineating the Genetic Basis of RNF213-related vasculopathies: The association of PKHD1 variants with bilateral cerebral vasculopathyDaiichiro Ishigami, Shinichi Namba, Satoru Miyawaki, et al.
Journal of Human Genetics|January 14, 2022
Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatmentsTakaki Taniguchi, Masahiro Ando, Yuji Okamoto, et al.
Neurology|January 28, 2014
Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in JapanMegumi Yamada, Masaki Tanaka, Mari Takagi, et al.
Journal of Human Genetics|January 29, 2022
An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese familiesMasahiro Ando, Yujiro Higuchi, Yuji Okamoto, et al.
Scientific Reports|October 10, 2025
RNF213 c.14429G > A (p.Arg4810Lys) is associated with non-arteritic retinal artery occlusionDaisuke Shimada, Satoru Miyawaki, Kaoru Nakanishi, et al.
Pageof 17