Behçet disease is an idiopathic, multisystem, chronic, and recurrent disease characterized
by exacerbations alternating with phases of quiescence, episodic panuveitis, and …

Behçet's disease (BD) is a systemic vasculitis disorder of unknown etiology, characterized
by relapsing episodes of oral aphthous ulcers, genital ulcers, skin lesions and ocular …

Several new treatment modalities with different mechanisms of action have been studied in
patients with Behçet's syndrome (BS). The aim of the current effort was to update the …

Objectives: To develop evidence-based European League Against Rheumatism (EULAR)
recommendations for the management of Behçet disease (BD) supplemented where …

T-helper type 17 cells (TH17) are implicated in rodent models of immune-mediated
diseases. Here we report their involvement in human uveitis and scleritis, and validate our …

Topic An international, expert-led consensus initiative to develop systematic, evidence-
based recommendations for the treatment of noninfectious uveitis in the era of biologics …

Behçet's disease (BD) is a systemic disorder characterized by recurrent attacks of acute
inflammation. Major symptoms are oral aphthous ulcers, uveitis, skin lesions, and genital …

Objective To assess the efficacy and safety of treatment modalities for major organ
involvement of Behçet's syndrome (BS), in order to inform the update of the EULAR …

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 …

Behçet's disease (BD) is a chronic, relapsing inflammatory, multisystem disease of unknown
etiology. The disease has a wide clinical spectrum of mucocutaneous lesions and ocular …