Behçet's disease (BD) is a chronic, relapsing, inflammatory multisystem disease of unknown
etiology. Oral ulcers, genital ulcers, cutaneous lesions, and ocular and articular involvement …

Behçet's disease (BD) is a systemic inflammatory disease with a chronic, relapsing-remitting
course of unknown etiology hallmarked predominantly by mucocutaneous lesions and …

Since 2010, next‐generation sequencing platforms have laid the foundation to an exciting
phase of discovery in oral microbiology as it relates to oral and systemic health and disease …

The spondyloarthropathies comprise ankylosing spondylitis (AS), reactive arthritis, psoriatic
arthritis (PsA) and arthritis associated with inflammatory bowel disease. In this Perspectives …

Behçet's disease is a chronic multisystem inflammatory disorder characterized mainly by
recurrent oral ulcers, ocular involvement, genital ulcers, and skin lesions, presenting with …

Abstract We analyzed 1,900 Turkish Behçet's disease cases and 1,779 controls genotyped
with the Immunochip. The most significantly associated SNP was rs1050502, a tag SNP for …

Takayasu arteritis is a rare inflammatory disease of large arteries. The etiology of Takayasu
arteritis remains poorly understood, but genetic contribution to the disease pathogenesis is …

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 …

The HLA protein, HLA-B* 51, encoded by HLA-B in MHC, is the strongest known genetic risk
factor for Behçet disease (BD). Associations between BD and other factors within the MHC …

Behçet disease is a chronic inflammatory systemic disorder, characterized by a relapsing
and remitting course. It manifests with oral and genital ulcerations, skin lesions, uveitis, and …