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 a rare systemic vasculitis characterized by oral aphthous ulcers,
genital ulcers, ocular lesions and other systemic manifestations. BD occurs most frequently …

Neuro-Behcet's disease (NBD) is defined as a combination of neurologic symptoms and/or
signs in a patient with Behcet's disease (BD). Relevant syndromes include brainstem …

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 …

Introduction Behcet's syndrome (BS) is a complex, heterogeneous disorder. However,
classification of its subgroups is still debated. The purpose of this study was to investigate …

Simple Summary The pathogenesis of autoimmune diseases etiology is still mostly unclear
and probably arises from an interplay between common/rare genetic variants and …

Purpose To review the pathogenesis of uveitis in light of recent advances in our
understanding of innate and adaptive immune responses and their regulation. Design …

Behçet's syndrome (BS) is a multisystemic vasculitis, characterized by different clinical
involvements, including mucocutaneous, ocular, vascular, neurological, and gastrointestinal …

Behçet's syndrome (BS) is a rare systemic vasculitis, characterized by a wide range of
different clinical involvements and unpredictable phases of recurrence and remission. BS …

Abstract Background The diagnosis of Behçet disease (BD) is challenging in many cases.
The purpose of this study was to describe the clinical characteristics of patients at a referral …