Responses
Other content recommended for you
- Behçet's disease
- A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease
- Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease
- Clinical and demographic evaluation of Behçet disease among different paediatric age groups
- Behçet’s disease presenting as recurrent oral aphthosis in a 9-year-old boy from Greece
- Acquired urethral meatal stenosis: a rare sequel of an aggressive form of Behçet's disease
- Familial aggregation of Behçet's disease in Turkey
- Rare presentation of thrombosis with bleeding in Behcet’s disease
- A rare case of Behçet disease with generalised myositis, cardiomyositis and necrotising fasciitis
- Large pulmonary artery pseudoaneurysm in a patient with Behçet’s disease treated with an Amplatzer vascular plug