Performance of diagnostic criteria in pediatric Behçet’s disease

Author:

Kurt TubaORCID,Aydın FatmaORCID,Sezer MügeORCID,Tekgöz P. NilüferORCID,Tekin Zahide EkiciORCID,Çelikel ElifORCID,Karagöl CüneytORCID,Coşkun SerkanORCID,Acar BanuORCID

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy,Rheumatology

Reference18 articles.

1. Hatemi G, Seyahi E, Fresko I, Talarico R, Hamuryudan V (2019) One year in review 2019: Behçet’s syndrome. Clin Exp Rheumatol 37(Suppl 121):3–17

2. Shahram F, Nadji A, Akhlaghi M, Faezi ST, Chams-Davatchi C, Shams H et al (2018) Pediatric Behçet’s disease in Iran: report of 204 cases. Clin Exp Rheumatol 36(6 Suppl 115):135–140

3. Ishido T, Horita N, Takeuchi M, Kawagoe T, Shibuya E, Yamane T et al (2017) Clinical manifestations of Behçet’s disease depending on sex and age: results from Japanese nationwide registration. Rheumatology (Oxford) 56(11):1918–1927

4. Karincaoglu Y, Borlu M, Toker SC, Akman A, Onder M, Gunastı S et al (2008) Demographic and clinical properties of juvenile-onset Behçet’s disease: a controlled multicenter study. J Am Acad Dermatol 58(4):579–584

5. Rodríguez-Carballeira M, Solans R, Larrañaga JR, García-Hernández FJ, Rios-Fernández R, Nieto J et al (2018) Venous thrombosis, and relapses in patients with Behçet’s disease. Descriptive analysis from Spanish network of Behçet’s disease (REGEB cohort). Clin Exp Rheumatol. 36(6 Suppl):40–44

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