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 characterised by recurrent episodes of orogenital aphthae,
systemic vasculitis, and systemic and retinal venous thrombosis. An association between …

Behçet syndrome is a multisystem vasculitis charac-terized by recurrent aphthous ulcers of
the mouth and genitalia, hyperreactivity of the skin to penetrating trauma (pathergy reaction) …

Behçet's disease (BD) is a multi-systemic inflammatory disorder which can affect all types
and sizes of blood vessels. This study aims to evaluate the prevalence and characteristics of …

Behcet's Disease (BD) is a systemic vasculitis characterized by the triad of recurrent mouth
and genital ulcers with eye involvement. To date there are no laboratory tests specific for the …

Objective. We investigated the effect of gender on the clinical Adamantiades–Behçet's
disease (ABD) phenotype with data from the German ABD registry and a meta-analysis from …

Behcet's disease (BD) is a chronic systemic inflammatory disorder characterized by
underlying chronic vasculitis of both large-and small-caliber vessels. Thoracic involvement …

The past year has seen some notable publications in the field of vasculitis epidemiology.
The appearance of reports from several different parts of the world has permitted …

Objectives.–To describe the features, prognosis, and treatment of vascular involvement in
Behçet's disease (BD). Patients.–Among 140 patients with BD seen at the Hôtel-Dieu …

The relationship between Behçet's disease (BD) and platelet aggregation has not sufficiently
been investigated yet. Mean platelet volume (MPV) is a marker of platelet function, and the …