Behçet syndrome is a rare, chronic inflammatory disease of unknown aetiopathogenesis,
most commonly presenting with mucocutaneous and ocular manifestations. Vascular …

Behçet's disease (BD) is a rare systemic vasculitis characterized by oral aphthous ulcers,
genital ulcers, ocular lesions and other systemic manifestations. BD occurs most frequently …

Behçet's disease (BD) is a chronic vasculitis characterized by systemic immune aberrations.
However, a comprehensive understanding of immune disturbances in BD and how they …

Behçet's disease (BD) is a systemic inflammatory disease with a chronic, relapsing-remitting
course of unknown etiology hallmarked predominantly by mucocutaneous lesions and …

Behçet’s Syndrome | New England Journal of Medicine Skip to main content Access provided
byKuopion Yliopistollinen Sairaala The New England Journal of Medicine homepage Advanced …

Background The small-molecule phosphodiesterase 4 inhibitor apremilast modulates
cytokines that are up-regulated in Behçet's syndrome. In a phase 2 trial involving patients …

Behçet's syndrome (BS) is a systemic vasculitis characterized by a relapsing and remitting
course. It can involve the skin, mucosa, joints, vessels (arteries and/or veins), eyes, and …

Introduction Behcet's syndrome (BS) is a complex, heterogeneous disorder. However,
classification of its subgroups is still debated. The purpose of this study was to investigate …

Behçet syndrome is a systemic vasculitis with an unknown aetiology affecting the small and
large vessels of the venous and arterial systems. The presence of symptom clusters …

Behçet syndrome (BS) is a multi-systemic complex disorder with unknown etiology and a
unique geographic distribution. It could not be possible to include it into specific …