Adult-Onset Still’s Disease (AOSD): Advances in Understanding Pathophysiology, Genetics and Emerging Treatment Options
Author:
Funder
Università degli Studi di Padova
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s40265-024-01993-x.pdf
Reference165 articles.
1. Sfriso P, Bindoli S, Galozzi P. Adult-Onset still’s disease: molecular pathophysiology and therapeutic advances. Drugs. 2018;78:1187–95. https://doi.org/10.1007/s40265-018-0956-9.
2. Nirmala N, Brachat A, Feist E, et al. Gene-expression analysis of adult-onset Still’s disease and systemic juvenile idiopathic arthritis is consistent with a continuum of a single disease entity. Pediatr Rheumatol. 2015;13:50. https://doi.org/10.1186/s12969-015-0047-3.
3. Kudela H, Drynda S, Lux A, et al. Comparative study of Interleukin-18 (IL-18) serum levels in adult onset Still’s disease (AOSD) and systemic onset juvenile idiopathic arthritis (sJIA) and its use as a biomarker for diagnosis and evaluation of disease activity. BMC Rheumatol. 2019;3:4. https://doi.org/10.1186/s41927-019-0053-z.
4. Pay S, Türkçapar N, Kalyoncu M, et al. A multicenter study of patients with adult-onset Still’s disease compared with systemic juvenile idiopathic arthritis. Clin Rheumatol. 2006;25:639–44. https://doi.org/10.1007/s10067-005-0138-5.
5. Li S, Ying S, Bai J, et al. Clinical characteristics and outcome of elderly onset adult-onset Still’s disease: a 10-year retrospective study. J Transl Autoimmun. 2023;6: 100196. https://doi.org/10.1016/j.jtauto.2023.100196.
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