Adult-onset Still disease: a rare disorder with a potentially fatal outcome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Rheumatology
Link
http://link.springer.com/content/pdf/10.1007/s13317-010-0009-1.pdf
Reference62 articles.
1. Ohta A, Yamaguchi M, Kaneoka H et al (1987) Adult Still’s disease: review of 228 cases from the literature. J Rheumatol 14:1139–1146
2. Ohta A, Yamaguchi M, Tsunematsu T et al (1990) Adult Still’s disease: a multicenter survey of Japanese patients. J Rheumatol 17:1058–1063
3. Efthimiou P, Paik PK, Bielory L (2006) Diagnosis and management of adult onset Still’s disease. Ann Rheum Dis 65:564–572
4. Kàdàr J, Petrovicz E (2004) Adult-onset Still’s disease. Best Practice & Research Clinical Rheumatology 18:663–676
5. Chen DY, Lan JL, Lin FJ et al (2004) Predominance of Th1 cytokine in peripheral blood and pathological tissues of patients with active untreated adult onset Still’s disease. Ann Rheum Dis 63:1300–1306
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1. Bibliometrics analysis on the research status and trends of adult-onset Still’s disease: 1921-2021;Frontiers in Immunology;2022-07-18
2. Biomarker screening and validation for the differentiation of bloodstream infection from adult-onset Still’s disease: A prospective cohort study;Cytokine;2021-10
3. Combination value of biomarkers in discriminating adult onset Still’s disease and sepsis;Wiener klinische Wochenschrift;2020-05-20
4. AA amyloidosis secondary to adult onset Still's disease: About 19 cases;Seminars in Arthritis and Rheumatism;2020-02
5. Anakinra Drug Retention Rate and Predictive Factors of Long-Term Response in Systemic Juvenile Idiopathic Arthritis and Adult Onset Still Disease;Frontiers in Pharmacology;2019-08-23
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