Diagnosing macrophage activation syndrome in systemic JIA
Author:
Publisher
Springer Science and Business Media LLC
Subject
Rheumatology
Link
http://www.nature.com/articles/nrrheum.2014.143.pdf
Reference10 articles.
1. Davi, S. et al. Performance of current guidelines for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis. Arthritis Rheum. http://dx.doi.org/10.1002/art.38769 .
2. Janka, G. E. Familial and acquired hemophagocytic lymphohistiocytosis. Annu. Rev. Med. 63, 233–246 (2012).
3. Mellins, E. D., Macaubas, C. & Grom, A. A. Pathogenesis of systemic juvenile idiopathic arthritis: some answers, more questions. Nat. Rev. Rheumatol. 7, 416–426 (2011).
4. de Jager, W. et al. Defective phosphorylation of interleukin-18 receptor β causes impaired natural killer cell function in systemic-onset juvenile idiopathic arthritis. Arthritis Rheum. 60, 2782–2793 (2009).
5. Henter, J. I. et al. HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr. Blood Cancer 48, 124–131 (2007).
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