« Previous
Next »
Best Practice & Research Clinical Rheumatology
Volume 20, Issue 4
, Pages 627-640
, August 2006
A child with a systemic febrile illness – differential diagnosis and management
References
- . Worldwide prevalence of juvenile arthritis: why does it vary so much?. The Journal of Rheumatology. 2002;29:1520–1530
- . Classification of childhood arthritis. Best Practice & Research. Clinical Rheumatology. 2002;16:379–396
- . Comparative epidemiology of the rheumatic diseases in children. Current Opinion in Rheumatology. 2000;12:410
- . The incidence of paediatric rheumatic diseases: results from the Canadian Paediatric Rheumatology Association Disease Registry. The Journal of Rheumatology. 1996;23:1981–1987
- The prevalence of familial Mediterranean fever in the Turkish province of Denizli: a field study with a zero patient design. Clinical and Experimental Rheumatology. 2004;22(supplement 34):S27–S30
- . Juvenile idiopathic arthritides evaluated prospectively in a single center according to the Durban criteria. The Journal of Rheumatology. 2001;28:1083–1090
- . ‘Adolescent-onset Still's disease’: characteristics and outcome in comparison with adult-onset Still's disease. Clinical and Experimental Rheumatology. 2002;19:427–430
- Acute hypoxic respiratory failure as the first manifestation of systemic-onset juvenile rheumatoid arthritis in a child. Pediatric Pulmonology. 2004;38:483–487
- Pediatric Rheumatology European Society clinical guidelines: systemic arthritis. Pediatric Rheumatology Online Journal. 2004;2:336–345
- Efficacy of etanercept for the treatment of juvenile idiopathic arthritis according to the onset type. Arthritis and Rheumatism. 2003;48:1093–1101
- Role of interleukin-1 (IL-1) in the pathogenesis of systemic onset juvenile idiopathic arthritis and clinical response to IL-1 blockade. The Journal of Experimental Medicine. 2005;201:1479–1486
- . Dynamics of fever and the cytokine network in systemic juvenile arthritis. Revue du Rhumatisme (English ed.). 1996;63:163–170
- . Diagnostic value of anti-neutrophil cytoplasmic and anti-endothelial cell antibodies in early Kawasaki disease. The Journal of Pediatrics. 1994;124:917–920
- . Pathogenesis and treatment of Kawasaki's disease. Current Opinion in Rheumatology. 2005;17:617–623
- Criteria for diagnosis of Behcet's disease. International Study Group for Behcet's Disease. Lancet 1990; 335: 1078–1080.
- . Polyarteritis nodosa associated with streptococcus. Archives of Disease in Childhood. 1993;69:685–688
- . Aspects nosologique des formes systémiques d'arthrite juvénile à début très précoce. A propos de 17 cas. La Semaine des Hôpitaux. 1984;60:163–167
- The spectrum of familial Mediterranean fever gene mutations in Arabs: report of a large series. Seminars in Arthritis and Rheumatism. 2005;34:813–818
- Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Medicine (Baltimore). 2005;84:1–11
- A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patients. Scandinavian Journal of Rheumatology. 1987;66(supplement):57–68
- . Chronic infantile neurological cutaneous and articular syndrome -- an early description. The Journal of Rheumatology. 2006;33:822–824
- . Urticaria, deafness and amyloidosis: a new heredo-familial syndrome. The Quarterly Journal of Medicine. 1962;31:235–248
- . A case of cold urticaria with unusual family history. JAMA. 1940;114:1067–1068
- Identification of a locus on chromosome 1q44 for familial cold urticaria. American journal of Human Genetics. 2000;66:1693–1698
- Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes. American Journal of Human Genetics. 2002;71:198–203
- Hyperimmunoglobulinaemia D and periodic fever: a new syndrome. Lancet. 1984;323:1087–1090
- . International Hyper-IgD Study Group. Hyperimmunoglobulinemia D and periodic fever syndrome: the clinical spectrum in a series of 50 patients. Medicine. 1994;73:133–144
- Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome. Nature Genetics. 1999;22:175–177
- International Hyper-IgD Study Group. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. Nature Genetics. 1999;22:178–181
- Familial Hibernian fever. The Quarterly Journal of Medicine. 1982;51:469–480
- Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell. 1999;97:133–144
- Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes. Arthritis and Rheumatism. 2003;48:2632–2644
- . Periodic fever syndrome in children. The Journal of Pediatrics. 1999;135:15–21
- . Paediatric Castleman disease: report of 7 cases and review of the literature. European Journal of Pediatrics. 1999;158:631–637
PII: S1521-6942(06)00042-8
doi: 10.1016/j.berh.2006.04.001
© 2006 Elsevier Ltd. All rights reserved.
« Previous
Next »
Best Practice & Research Clinical Rheumatology
Volume 20, Issue 4
, Pages 627-640
, August 2006
