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

The term “vasculitis” refers to a group of rare immune‐mediated diseases characterized by
the dysregulated immune system attacking blood vessels located in any organ of the body …

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

Systemic vasculitides are autoimmune diseases characterized by inflammation of blood
vessels. Their categorization is based on the size of the preferentially affected blood vessels …

Autoimmune diseases have specific pathophysiologic mechanisms leading to an increased
risk of arterial and venous thrombosis. The risk of venous thromboembolism (VTE) varies …

Behçet Disease is a relapsing and remitting variable vessel vasculitis characterized by
recurrent mucocutaneous ulcers that can involve almost every organ system in the body …

Behçet's disease is a rare and poorly understood vasculitis affecting blood vessels of all
types and sizes. Uveitis and oral and genital ulcers represent the typical clinical triad …

Behçet's disease (BD) is a multifaceted autoimmune disorder affecting multiple organ
systems. Vascular complications, such as venous thromboembolism (VTE), are highly …

Opinion statement• Clinical and imaging data suggest that Behçet's disease (BD) can
present with a variety of neurologic complications, which may be subclassified into two …

To evaluate the intima media thickness of carotid arteries (IMT) and its clinical, laboratory
and treatment correlates in Behcet's disease (BD). Systematic search of EMBASE and …