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Michio Inoue

Showing results (51-60 of 57) with videos related to

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JAMA Neurology|April 21, 2020
Association of Dermatomyositis Sine Dermatitis With Anti-Nuclear Matrix Protein 2 AutoantibodiesMichio Inoue, Jantima Tanboon, Shinya Hirakawa, et al.
Acta Neuropathologica|October 20, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureConrad C Weihl, Ana Töpf, Rocio Bengoechea, et al.
Acta Neuropathologica Communications|October 30, 2019
Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairmentPascal Laforêt, Michio Inoue, Evelyne Goillot, et al.
Brain : a Journal of Neurology|September 28, 2021
MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline elevated  serum creatine kinaseOsorio Lopes Abath Neto, Livija Medne, Sandra Donkervoort, et al.
Neurology. Genetics|August 17, 2023
Clinical Classification of Variants in the Valosin-Containing Protein Gene Associated With Multisystem ProteinopathyMarianela Schiava, Chiseko Ikenaga, Ana Topf, et al.
Cell Stress & Chaperones|December 21, 2025
J-domain proteins: from molecular mechanisms to diseasesJanine Kirstein, Rina Rosenzweig, Paolo De Los Rios, et al.
Neurology. Genetics|July 18, 2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem ProteinopathyMarianela Schiava, Yolande Parkhurst, Matthew Henderson, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
JAMA Neurology|April 21, 2020
Association of Dermatomyositis Sine Dermatitis With Anti-Nuclear Matrix Protein 2 AutoantibodiesMichio Inoue, Jantima Tanboon, Shinya Hirakawa, et al.
Acta Neuropathologica|October 20, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureConrad C Weihl, Ana Töpf, Rocio Bengoechea, et al.
Acta Neuropathologica Communications|October 30, 2019
Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairmentPascal Laforêt, Michio Inoue, Evelyne Goillot, et al.
Brain : a Journal of Neurology|September 28, 2021
MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline elevated  serum creatine kinaseOsorio Lopes Abath Neto, Livija Medne, Sandra Donkervoort, et al.
Neurology. Genetics|August 17, 2023
Clinical Classification of Variants in the Valosin-Containing Protein Gene Associated With Multisystem ProteinopathyMarianela Schiava, Chiseko Ikenaga, Ana Topf, et al.
Cell Stress & Chaperones|December 21, 2025
J-domain proteins: from molecular mechanisms to diseasesJanine Kirstein, Rina Rosenzweig, Paolo De Los Rios, et al.
Neurology. Genetics|July 18, 2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem ProteinopathyMarianela Schiava, Yolande Parkhurst, Matthew Henderson, et al.
Pageof 6