Behçet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic vasculitis
characterized by recurrent oral and genital aphthous ulcers, ocular disease and skin lesions …

Behçet's disease is a systemic vasculitis characterized by attacks of acute inflammation,
which can affect almost every vascularized area of the body. There is a close correlation …

The current proposal for cerebral venous thrombosis guideline followed the Grading of
Recommendations, Assessment, Development, and Evaluation system, formulating relevant …

Background Oral ulcers, the hallmark of Behçet's syndrome, can be resistant to conventional
treatment; therefore, alternative agents are needed. Apremilast is an oral phosphodiesterase …

Objective To report the efficacy and safety of anti-TNF agents in patients with severe and/or
refractory manifestations of Behçet's disease (BD). Methods We performed a multicenter …

Objectives Behçet's disease (BD) is a chronic systemic vasculitis. Thrombosis is a frequent
and life-threatening complication. The pathogenesis of BD is poorly understood and …

Behçet's disease is a multisystem disorder with unknown etiology and a unique geographic
distribution. The disease is characterized by recurrent skin–mucosa lesions and sight …

Behçet disease is currently considered an “autoinflammatory disease” triggered by infection
and environmental factors in genetically predisposed individuals. Although the disease is …

Objective To investigate and describe the long‐term outcome of venous thrombosis in
patients with Behçet's disease (BD). Methods In a retrospective cohort of 807 BD patients, a …

Behçet disease is a chronic inflammatory systemic disorder, characterized by a relapsing
and remitting course. It manifests with oral and genital ulcerations, skin lesions, uveitis, and …