Objective. To investigate comprehensively the relationships between Behçet's disease (BD)
clinical features and HLA-B51 or HLA-B5 (HLA-B51/B5) status using meta-analyses …

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 …

The aim of this study was to compare the efficacy of immunosuppressive therapy alone with
that of combination therapy involving immunosuppressants and anticoagulation for the …

Behçet's disease is characterized by recurrent aphthous stomatitis, uveitis, genital ulcers,
and skin lesions. The role of the HLA-B* 51 gene has been confirmed in recent years …

Objectives. To analyze demographic, clinical and genetic features of Behçet's disease (BD)
in Tunisia and to'compare them with other ethnic and geographic groups. Methods. Two …

Introduction There is good evidence that specific autoimmune rheumatic diseases (RDs), for
example, rheumatoid arthritis and systemic lupus erythematosus (SLE), are associated with …

OBJECTIVES: Budd–Chiari syndrome is a rare and serious complication of Behçet's
disease, and is the result of occlusion of the major hepatic veins, the adjacent inferior vena …

Herein, we report 3 cases of Behçet syndrome that were accompanied by intracardiac
thrombus. The 1st patient was a 30-year-old man who presented with dyspnea; a right atrial …

Objective. Vascular lesions can involve both arterial and venous systems which are often the
major causes complicating the disease course of Behçet's disease (BD). Vascular …

Background and aim Behçet's syndrome (BS) is a known cause of Budd-Chiari syndrome
(BCS). We aimed at identifying the prevalence of BS in patients with BCS, analyzing different …