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 immune-mediated vasculitis of unclear origin. Major
symptoms include oral aphthous ulcers, genital ulcerations, skin lesions, and ocular lesions …

Behcet's Disease (BD) is a systemic vasculitis of unknown etiology. Increasing studies find
that a sophisticated interlacing cytokine network is closely implicated in the onset, evolution …

The study objective was to report treatment with an interleukin (IL)-1 receptor antagonist,
anakinra, in patients with multiorgan Behcet's disease (BD). Comparison of clinical …

Increased cerebrospinal fluid (CSF) IL-6 has been reported in patients with Behçet's disease
(BD) and neurological involvement. To elucidate the value of IL-6 as a marker of disease …

Behçet's disease (BD) is a systemic inflammatory disease characterized by recurrent oral
ulcers, genital ulcers, cutaneous inflammation, and uveitis. In addition, other potentially life …

Purpose To study the intraocular and serum cytokine and chemokine profile in patients with
intermediate uveitis (IU) at various stages of inflammatory activity. Methods Institutional …

Background Genetic factors that predispose individuals to Behçet's disease (BD) are
considered to play an important role in development of the disease. The tumour necrosis …

Behçet's disease (BD) is a chronic systemic vasculitis characterized by recurrent oral and
genital ulcers, skin lesions, articular, neurological, vascular and sight-threatening ocular …

Interleukin 37 has been found to play a significant regulatory role in the innate immune
response. It is not yet known whether IL-37 has also been involved in the development of …