1. Davatchi F, Chams-Davatchi C, Shams H, et al. Behcet's disease: epidemiology, clinical manifestations, and diagnosis. Expert Rev ClinImmunol. 2017;13(1):57-65. [
DOI:10.1080/1744666X.2016.1205486]
2. Alpsoy E. Behcet's disease: A comprehensive review with a focus on epidemiology, etiology and clinical features, and management of mucocutaneous lesions. J Dermatol. 2016;43(6):620-32. [
DOI:10.1111/1346-8138.13381]
3. Esatoglu SN, Kutlubay Z, Ucar D, et al. Behcet's syndrome: providing integrated care. J Multidiscip Health Care2017;10:309-19. [
DOI:10.2147/JMDH.S93681]
4. Khabbazi A, KarkonShayan F, Ghojazadeh M, et al. Adherence to treatment in patients with Behcet's disease. Int J Rheumat Dis. 2018;21(12):2158-66. [
DOI:10.1111/1756-185X.13109]
5. Kilian NC, Sawalha AH. Behcet's disease in the United States: A single center descriptive and comparative study. Europ J Rheumatol. 2017;4(4):239-44. [
DOI:10.5152/eurjrheum.2017.17112]
6. Mat MC, Sevim A, Fresko I, Tuzun Y. Behcet's disease as a systemic disease. ClinDermatol. 2014;32(3):435-42. [
DOI:10.1016/j.clindermatol.2013.11.012]
7. Shahriyari E, Bonyadi M, JabbarpoorBonyadi MH, Soheilian M, Yaseri M, Ebrahimiadib N. Ubiquitin associated and SH3 domain containing B (UBASH3B) gene association with Behcet's disease in Iranian population. Curr Eye Res. 2019;44(2):200-5. [
DOI:10.1080/02713683.2018.1524913]
8. Scherrer MAR, Rocha VB, Garcia LC. Behcet's disease: review with emphasis on dermatological aspects. Anais brasileiros de dermatologia. 2017;92(4):452-64. [
DOI:10.1590/abd1806-4841.20177359]
9. Davari P, Rogers RS, Chan B, Nagler TH, Fazel N. Clinical features of Behcet's disease: A retrospective chart review of 26 patients. J Dermatol Treat. 2016;27(1):70-4. [
DOI:10.3109/09546634.2015.1054781]
10. Kiss E, Dohan J, Nemeth J, Poor G. Behcet's disease: a rarely recognized orphan disorder. Orvosihetilap. 2013;154(3):93-101. [
DOI:10.1556/OH.2013.29528]
11. Saccucci M, Di Carlo G, Bossu M, Giovarruscio F, Salucci A, Polimeni A. Autoimmune diseases and their manifestations on oral cavity: diagnosis and clinical management. J Immunol Res. 2018;2018:6061825. [
DOI:10.1155/2018/6061825]
12. Munoz SA, Orden AO, Kostianovsky A, et al. The HLA-B*51 allele is strongly associated with Behcet disease in an argentinean population. ReumatolClin. 2020;16(4):282-85 [
DOI:10.1016/j.reuma.2018.07.002]
13. Maldini C, Lavalley MP, Cheminant M, de Menthon M, Mahr A. Relationships of HLA-B51 or B5 genotype with Behcet's disease clinical characteristics: systematic review and meta-analyses of observational studies. Rheumatol (Oxford, England). 2012;51(5):887-900. [
DOI:10.1093/rheumatology/ker428]
14. Ryu HJ, Seo MR, Choi HJ, Baek HJ. Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51. Korean J Int Med. 2018;33(5):1025-31. [
DOI:10.3904/kjim.2016.202]
15. Hamzaoui A, Houman MH, Massouadia M, et al. Contribution of Hla-B51 in the susceptibility and specific clinical features of Behcet's disease in Tunisian patients. Europ J IntMed. 2012;23(4):347-9. [
DOI:10.1016/j.ejim.2011.12.011]
16. Demirseren DD, Ceylan GG, Akoglu G, et al. HLA-B51 subtypes in Turkish patients with Behcet's disease and their correlation with clinical manifestations. Genet Molec Res. 2014;13(3):4788-96. [
DOI:10.4238/2014.July.2.8]
17. The International Criteria for Behcet's Disease (ICBD): a collaborative study of 27 countries on the sensitivity and specificity of the new criteria. J EuropAcadDermatolVenereol . 2014;28(3):338-47. [
DOI:10.1111/jdv.12107]
18. Kanecki K, Nitsch-Osuch A, Gorynski P, Tarka P, Kutera A, Tyszko P. Behcet disease: a rare systemic vasculitis in Poland. Polish archives of internal medicine. 2017;127(10):652-6. [
DOI:10.20452/pamw.4160]
19. Wang ZK, Shi H, Wang SD, et al. Confusing untypical intestinal Behcet's disease: Skip ulcers with severe lower gastrointestinal hemorrhage. World J GastrointestEndoscop. 2014;6(1):27-31. [
DOI:10.4253/wjge.v6.i1.27]
20. Zeidan MJ, Saadoun D, Garrido M, Klatzmann D, Six A, Cacoub P. Behcet's disease physiopathology: a contemporary review. Auto Immun Highlights. 2016;7(1):4. [
DOI:10.1007/s13317-016-0074-1]
21. Taylor J, Glenny AM, Walsh T, et al. Interventions for the management of oral ulcers in Behcet's disease. Cochrane Database System Rev. 2014(9):Cd011018. [
DOI:10.1002/14651858.CD011018]
22. Tunes RS, Anjos TC, Martins GB, Barreto ER, Santiago MB. Prevalence of Behcet's syndrome in patients with recurrent aphthous ulcerations in Brazil. Rheumatol Int. 2009;29(8):875-8. [
DOI:10.1007/s00296-008-0787-1]
23. Lennikov A, Alekberova Z, Goloeva R, et al. Single center study on ethnic and clinical features of Behcet's disease in Moscow, Russia. ClinRheumatol. 2015;34(2):321-7. [
DOI:10.1007/s10067-013-2442-9]
24. Ghembaza ME, Bouabdallah N, Lounici A. Behcet disease in Western Algeria. Medecine et santetropicales. 2017;27(1):101-4. [
DOI:10.1684/mst.2017.0656]
25. Bergamo S, di Meo N, Stinco G, Bonin S, Trevisini S, Trevisan G. Adamantiades-Behcet disease at the beginning of the silk route: North-East Italian Experience. ActadermatovenerolCroatica : ADC. 2017;25(4):295-7.
26. Suzuki T, Horita N, Takeuchi M, et al. Clinical features of early-stage possible Behcet's disease patients with a variant-type major organ involvement in Japan. Modern Rheumatol. 2018:1-7.
27. Kim JN, Kwak SG, Choe JY, Kim SK. The prevalence of Behcet's disease in Korea: data from health insurance review and assessment service from 2011 to 2015. Clin Experiment Rheumatol. 2017;35Suppl 108(6):38-42.
28. Sibley C, Yazici Y, Tascilar K, et al. Behcet syndrome manifestations and activity in the United States versus Turkey -- a cross-sectional cohort comparison. J Rheumatol. 2014;41(7):1379-84. [
DOI:10.3899/jrheum.131227]
29. Calamia KT, Wilson FC, Icen M, Crowson CS, Gabriel SE, Kremers HM. Epidemiology and clinical characteristics of Behcet's disease in the US: a population-based study. Arthritis Rheumatism. 2009;61(5):600-4. [
DOI:10.1002/art.24423]
30. Ugurlu N, Bozkurt S, Bacanli A, Akman-Karakas A, Uzun S, Alpsoy E. The natural course and factors affecting severity of Behcet's disease: a single-center cohort of 368 patients. Rheumatol Int. 2015;35(12):2103-7. [
DOI:10.1007/s00296-015-3310-5]
31. Cansu DU, Kasifoglu T, Korkmaz C. Do clinical findings of Behcet's disease vary by gender?: A single-center experience from 329 patients. Europ J Rheumatol. 2016;3(4):157-60. [
DOI:10.5152/eurjrheum.2016.038]
32. Ozyurt K, Colgecen E, Baykan H. Does familial occurrence or family history of recurrent oral ulcers influence clinical characteristics of Behcet's disease? ActadermatovenerologicaCroatica : ADC. 2013;21(3):168-73.
33. Sula B, Batmaz I, Ucmak D, Yolbas I, Akdeniz S. Demographical and clin characteristics of Behcet's disease in Southeastern Turkey. J Clin Med Res. 2014;6(6):476-81. [
DOI:10.14740/jocmr1952w]