Michio Inoue
Tokyo, Japan
Last Updated: 09/26/2026
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Found 45 publications
VMA21 deficiency leads to autophagic dysregulation and altered vesicle trafficking in X-linked myopathy with excessive autophagy.
Journal: Acta neuropathologica
Published: March 26, 2026
Molecular genetics of J-domain protein-related chaperonopathies in skeletal muscle.
Journal: Journal of human genetics
Published: July 06, 2025
Myofibrillar myopathy: towards a mechanism-based definition as a Z-disk-opathy.
Journal: Current opinion in neurology
Published: June 09, 2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy.
Journal: Neurology. Genetics
Published: November 26, 2024
Genotype-phenotype correlation in recessive DNAJB4 myopathy.
Journal: Research square
Published: November 01, 2024
Genotype‒phenotype correlation in recessive DNAJB4 myopathy.
Journal: Acta neuropathologica communications
Published: August 14, 2024
Association Between HLA Alleles and Autoantibodies in Dermatomyositis Defined by Sarcoplasmic Expression of Myxovirus Resistance Protein A.
Journal: The Journal of rheumatology
Published: May 19, 2023
A Case of Cardiogenic Stroke With a Novel LMNA Variant (c. 1135C>A; p.Leu379Ile).
Journal: Cureus
Published: April 19, 2023
Mechanistic characterization of disulfide bond reduction of an ERAD substrate mediated by cooperation between ERdj5 and BiP.
Journal: The Journal of biological chemistry
Published: March 10, 2023
A 53-year-old man with a 16-year history of asymmetrical proximal muscle weakness, facial muscle weakness, and scapular winging.
Journal: Brain pathology (Zurich, Switzerland)
Published: November 29, 2022
Last Updated: 09/26/2026