Secondary Causes of Myositis
Author:
Funder
The Peter and Carmen Lucia Buck Foundation
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology
Link
https://link.springer.com/content/pdf/10.1007/s11940-020-00646-0.pdf
Reference103 articles.
1. Greenberg SA. Inclusion body myositis: clinical features and pathogenesis. Nat Rev Rheumatol. 2019;15(5):257–72.
2. •• Allenbach Y, Mammen AL, Benveniste O, et al. 224th ENMC International Workshop: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14–16 October 2016. Neuromuscul Disord. 2018;28(1):87–99. This paper has recent expert consensus guidelines for treatment of anti-HMGCR antibody myopathy.
3. Mammen AL, Allenbach Y, Stenzel W, Benveniste O, Allenbach DY, Benveniste DO, et al. 239th ENMC International Workshop: classification of dermatomyositis, Amsterdam, the Netherlands, 14-16 December 2018. Neuromuscul Disord. 2020;30(1):70–92.
4. Noguchi E, Uruha A, Suzuki S, Hamanaka K, Ohnuki Y, Tsugawa J, et al. Skeletal muscle involvement in antisynthetase syndrome. JAMA Neurol. 2017;74(8):992–9.
5. Lloyd TE, Mammen AL, Amato AA, Weiss MD, Needham M, Greenberg SA. Evaluation and construction of diagnostic criteria for inclusion body myositis. Neurology. 2014;83(5):426–33.
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