A Childhood Inflammatory Myopathy with Cytochrome Oxidase Deficiency: Which Came First, the Chicken or the Egg?
Author:
Publisher
Galenos Yayinevi
Subject
General Medicine
Reference9 articles.
1. 1. Rider LG, Nistala K. The juvenile idiopathic inflammatory myopathies: pathogenesis, clinical and autoantibody phenotypes, and outcomes. J Intern Med. 2016;280(1):24-38. doi: 10.1111/joim.12444
2. 2. Stenzel W, Goebel HH, Bader-Meunier B, Gitiaux C. Inflammatory myopathies in childhood. Neuromuscul Disord. 2021;31(10):1051-61. doi: 10.1016/j.nmd.2021.08.007
3. 3. Papadimas GK, Kokkinis C, Xirou S, Chrysanthou M, Kararizou E, Papadopoulos C. Polymyositis with mitochondrial pathology or atypical form of sporadic inclusion body myositis: case series and review of the literature. Rheumatol Int. 2019;39(8):1459-66. doi: 10.1007/s00296-019-04314-8
4. 4. Kleefeld F, Uruha A, Schänzer A, Nishimura A, Roos A, Schneider U, et al. Morphologic and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body Myositis. Neurology. 2022;99(20):2212-22. doi: 10.1212/WNL.0000000000201103
5. 5. Schänzer A, Rager L, Dahlhaus I, Dittmayer C, Preusse C, Della Marina A, et al. Morphological Characteristics of Idiopathic Inflammatory Myopathies in Juvenile Patients. Cells. 2022;11(1):109. doi: 10.3390/cells11010109
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