A bibliometric analysis of idiopathic inflammatory myopathies from 1982 to 2021
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Rheumatology
Link
https://link.springer.com/content/pdf/10.1007/s10067-022-06437-z.pdf
Reference47 articles.
1. Mariampillai K, Granger B, Amelin D, Guiguet M, Hachulla E, Maurier F et al (2018) Development of a new classification system for idiopathic inflammatory myopathies based on clinical manifestations and myositis-specific autoantibodies. JAMA Neurol 75(12):1528–1537. https://doi.org/10.1001/jamaneurol.2018.2598
2. Lundberg IE, de Visser M, Werth VP (2018) Classification of myositis. Nat Rev Rheumatol 14(5):269–278. https://doi.org/10.1038/nrrheum.2018.41
3. Selva-O’Callaghan A, Pinal-Fernandez I, Trallero-Araguas E, Milisenda JC, Grau-Junyent JM, Mammen AL (2018) Classification and management of adult inflammatory myopathies. Lancet Neurol 17(9):816–828. https://doi.org/10.1016/S1474-4422(18)30254-0
4. Furst DE, Amato AA, Iorga SR, Gajria K, Fernandes AW (2012) Epidemiology of adult idiopathic inflammatory myopathies in a U.S. managed care plan. Muscle Nerve 45(5):676–683. https://doi.org/10.1002/mus.23302
5. Cho S-K, Kim H, Myung J, Nam E, Jung S-Y, Jang EJ et al (2019) Incidence and prevalence of idiopathic inflammatory myopathies in Korea: a nationwide population-based study. J Korean Med Sci 34(8):e55. https://doi.org/10.3346/jkms.2019.34.e55
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1. Autoimmune inflammatory myopathy biomarkers;Clinica Chimica Acta;2024-01
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