Novel Therapeutic Options in Treatment of Idiopathic Inflammatory Myopathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical)
Link
http://link.springer.com/article/10.1007/s11940-018-0521-6/fulltext.html
Reference112 articles.
1. •• Allenbach Y, Benveniste O, Goebel HHH, Stenzel W. Review: integrated classification of inflammatory myopathies. Neuropathol Appl Neurobiol. 2017;43(1):62–81. A comprehensive review of new myositis-associated and myositis-specific autoantibodies and their influence on muscle pathology. This review integrates the clinical phenotype, serological findings and histopathological findings into a unified classification of myositis.
2. Findlay AR, Goyal NA, Mozaffar T. An overview of polymyositis and dermatomyositis. Muscle Nerve. 2015;51(5):638–56.
3. Benveniste O, Stenzel W, Allenbach Y. Advances in serological diagnostics of inflammatory myopathies. Curr Opin Neurol. 2016;29(5):662–73.
4. Preuße C, Allenbach Y, Hoffmann O, Goebel H-HH, Pehl D, Radke J, et al. Differential roles of hypoxia and innate immunity in juvenile and adult dermatomyositis. Acta Neuropathol Commun. 2016;4(1):45.
5. • Ladislau L, Suárez-Calvet X, Toquet S, Landon-Cardinal O, Amelin D, Depp M, et al. JAK inhibitor improves type I interferon induced damage: proof of concept in dermatomyositis. Brain. 2018;141(6):1609–21. An important recent paper that highlights the role of interferon and JAK/STAT pathway in DM.
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