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

Behçet's syndrome (BS) is a complex vasculitis, characterised by peculiar histological,
pathogenetic and clinical features. Superficial venous thrombosis (SVT) and deep vein …

Behçet syndrome (BS) is a multisystem vasculitis with unknown etiology and a unique
geographic distribution. The disease course is characterized by exacerbations and …

Behçet's syndrome is a systemic vasculitis of unknown etiology involving the small and large
vessels of both the venous and arterial systems. Distinct clusters of disease expression have …

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's disease (BD) is a chronic inflammatory disease of unknown aetiology characterized
by recurrent oral, genital aphthous ulcerations, uveitis, skin lesions and other multisystem …

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 …

Behçet's syndrome is a variable vessel vasculitis with multi-system involvement that shows
important heterogeneity among patients regarding demographic features, organ …

Behçet's syndrome (BS) is a systemic vasculitis, clinically characterized by different organ
involvement and often complicated by thrombosis which occurs in vessels of all sizes …

Abstract Objective. Some features of Behçet's syndrome (BS) tend to go together. We aimed
to explore the association and timing of various vascular events in both the venous and the …