Juvenile idiopathic inflammatory myositis: an update on pathophysiology and clinical care
Author:
Publisher
Springer Science and Business Media LLC
Subject
Rheumatology
Link
https://www.nature.com/articles/s41584-023-00967-9.pdf
Reference232 articles.
1. Lundberg, I. E. et al. European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups. Arthritis Rheumatol. 69, 2271–2282 (2017).
2. Patel, B., Khan, N. & Werth, V. P. Applicability of EULAR/ACR classification criteria for dermatomyositis to amyopathic disease. J. Am. Acad. Dermatol. 79, 77–83.e1 (2018).
3. Bohan, A. & Peter, J. B. Polymyositis and dermatomyositis (second of two parts). N. Engl. J. Med. 292, 403–407 (1975).
4. Tansley, S. L. et al. Autoantibodies in juvenile-onset myositis: their diagnostic value and associated clinical phenotype in a large UK cohort. J. Autoimmun. 84, 55–64 (2017).
5. Rider, L. G. et al. The myositis autoantibody phenotypes of the juvenile idiopathic inflammatory myopathies. Medicine 92, 223–243 (2013).
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