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Jun Shimizu

Showing results (181-190 of 225) with videos related to

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Neurology(R) Neuroimmunology & Neuroinflammation|January 31, 2019
Inflammatory myopathy with myasthenia gravis: Thymoma association and polymyositis pathologyNaohiro Uchio, Kenichiro Taira, Chiseko Ikenaga, et al.
Journal of Molecular Neuroscience : MN|January 12, 2021
Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the LiteratureJunko Kanda Kikuchi, Yu Nagashima, Tatsuo Mano, et al.
ESC Heart Failure|September 6, 2022
The effect of immunosuppressive therapy on cardiac involvements in anti-mitochondrial antibody-positive myositisSatoshi Bujo, Eisuke Amiya, Meiko Hashimoto Maeda, et al.
Neurology. Genetics|September 3, 2025
Vanishing White Matter Disease With <i>EIF2B2</i> c.254 >A Variant: Mild Clinical and MRI FindingsToshiyuki Kakumoto, Takashi Matsukawa, Ryo Tokimura, et al.
Journal of Neuroimmunology|November 18, 2016
IgG4 anti-neurofascin155 antibodies in chronic inflammatory demyelinating polyradiculoneuropathy: Clinical significance and diagnostic utility of a conventional assayMasato Kadoya, Kenichi Kaida, Haruki Koike, et al.
Internal Medicine (Tokyo, Japan)|August 9, 2023
Late-onset Myoclonic Seizure in a 78-year-old Woman with Gaucher DiseaseNanaka Yamaguchi-Takegami, Akiko Takahashi, Jun Mitsui, et al.
Journal of the Neurological Sciences|December 27, 2016
Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencingTakashi Matsukawa, Kagari Mano Koshi, Jun Mitsui, et al.
Neurology. Genetics|October 27, 2025
Erratum: Vanishing White Matter Disease With <i>EIF2B2</i> c.254T>A Variant: Mild Clinical and MRI FindingsToshiyuki Kakumoto, Takashi Matsukawa, Ryo Tokimura, et al.
Mbio|June 23, 2025
Evolutionary dynamics of heparan sulfate utilization by SARS-CoV-2Shuhei Higuchi, Yafei Liu, Jun Shimizu, et al.
Cerebellum (London, England)|September 13, 2017
Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and DystoniaMasanori Kurihara, Hiroyuki Ishiura, Takuya Sasaki, et al.
Pageof 23

Showing results (181-190 of 225) with videos related to

Sort By:
Pageof 23
Neurology(R) Neuroimmunology & Neuroinflammation|January 31, 2019
Inflammatory myopathy with myasthenia gravis: Thymoma association and polymyositis pathologyNaohiro Uchio, Kenichiro Taira, Chiseko Ikenaga, et al.
Journal of Molecular Neuroscience : MN|January 12, 2021
Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the LiteratureJunko Kanda Kikuchi, Yu Nagashima, Tatsuo Mano, et al.
ESC Heart Failure|September 6, 2022
The effect of immunosuppressive therapy on cardiac involvements in anti-mitochondrial antibody-positive myositisSatoshi Bujo, Eisuke Amiya, Meiko Hashimoto Maeda, et al.
Neurology. Genetics|September 3, 2025
Vanishing White Matter Disease With <i>EIF2B2</i> c.254 >A Variant: Mild Clinical and MRI FindingsToshiyuki Kakumoto, Takashi Matsukawa, Ryo Tokimura, et al.
Journal of Neuroimmunology|November 18, 2016
IgG4 anti-neurofascin155 antibodies in chronic inflammatory demyelinating polyradiculoneuropathy: Clinical significance and diagnostic utility of a conventional assayMasato Kadoya, Kenichi Kaida, Haruki Koike, et al.
Internal Medicine (Tokyo, Japan)|August 9, 2023
Late-onset Myoclonic Seizure in a 78-year-old Woman with Gaucher DiseaseNanaka Yamaguchi-Takegami, Akiko Takahashi, Jun Mitsui, et al.
Journal of the Neurological Sciences|December 27, 2016
Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencingTakashi Matsukawa, Kagari Mano Koshi, Jun Mitsui, et al.
Neurology. Genetics|October 27, 2025
Erratum: Vanishing White Matter Disease With <i>EIF2B2</i> c.254T>A Variant: Mild Clinical and MRI FindingsToshiyuki Kakumoto, Takashi Matsukawa, Ryo Tokimura, et al.
Mbio|June 23, 2025
Evolutionary dynamics of heparan sulfate utilization by SARS-CoV-2Shuhei Higuchi, Yafei Liu, Jun Shimizu, et al.
Cerebellum (London, England)|September 13, 2017
Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and DystoniaMasanori Kurihara, Hiroyuki Ishiura, Takuya Sasaki, et al.
Pageof 23