Mitochondrial dysfunction in anti-3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) immune-mediated necrotising myopathy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference11 articles.
1. Immune-mediated necrotizing myopathy: clinical features and pathogenesis;Allenbach;Nat Rev Rheumatol,2020
2. Nonimmune mechanisms in idiopathic inflammatory myopathies;Loredo Martinez;Curr Opin Rheumatol,2020
3. Myositis non-inflammatory mechanisms: an up-dated review;Manole;J Immunoass Immunochem,2017
4. Mitophagy in three cases of immune-mediated necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase autoantibodies: ultrastructural and immunohistochemical studies;Matsubara;Neuromuscul Disord,2018
5. Sequestosome-1 (p62) expression reveals chaperone-assisted selective autophagy in immune-mediated necrotizing myopathies;Fischer;Brain Pathol,2020
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Effects of HMGCR deficiency on skeletal muscle development;2024-05-08
2. Comprehensive transcriptomic analysis and machine learning reveal unique gene expression profiles in patients with immune‐mediated necrotizing myopathy;The Journal of Gene Medicine;2023-09-25
3. Clinicopathological and circulating cell‐free DNA profile in myositis associated with anti‐mitochondrial antibody;Annals of Clinical and Translational Neurology;2023-09-18
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