Behçet disease is an idiopathic, multisystem, chronic, and recurrent disease characterized
by exacerbations alternating with phases of quiescence, episodic panuveitis, and …

Behçet's disease is a chronic inflammatory disorder of unknown aetiology characterised by
recurrent attacks. Although the triple symptom complex of oral and genital ulcerations with …

Autoinflammatory diseases are a group of heritable disorders that are characterized by
seemingly unprovoked episodes of inflammation at certain locations and and relative lack of …

Behçet's disease (BD) is an inflammatory disorder of unknown aetiology characterised by
recurrent attacks affecting the mucocutaneous tissues, eyes, joints, blood vessels, brain and …

Behçet's disease (BD) is a multisystemic inflammatory disorder. Although the cause and
pathogenesis of BD are still unclear, there is evidence for genetic, immunologic and …

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 …

Background Analysis of the T‐cell receptor (TCR)‐Vβ repertoire has been used for studying
selective T‐cell responses in autoimmune disease, alloreactivity in transplantation, and …

Behçet's disease (BD), originally described as oral and genital ulcers and uveitis, 1 is a
vasculitis that can involve any organ system. It is a commonly encountered health problem in …

Background: Heat shock protein (60 kd HSP) has been implicated in the etiology of Behçet's
disease, but its expression at sites of inflammation is unknown. Objective: Our aim was to …

Involvement of excessive Th1 cell functions and heat shock protein expression in the
pathogenesis of Behçet's disease (BD) has been reported. In this study we have …