Behçet's disease is a systemic vasculitis frequently associated with intraocular inflammation.
Recent findings identified independent clinical clusters in Behçet's disease, each involving …

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

To identify new genetic risk factors for Vogt-Koyanagi-Harada (VKH) syndrome, we
conducted a genome-wide association study of 2,208,258 SNPs in 774 cases and 2,009 …

GWAS data established a major step forward by providing insights into the underlying
mechanisms in Behçet's disease with the discovery of new susceptibility genes. These …

Neutrophils constitute essential players in inflammatory responses and are the first line of
defence against harmful stimuli. However, dysregulation of neutrophil homeostasis can …

Behçet's disease (BD) is universally recognized as a multisystemic inflammatory disease of
unknown etiology with chronic course and unpredictable exacerbations: its clinical spectrum …

Behçet's disease is a chronic multisystemic inflammatory disorder characterized by recurrent
oral and genital ulcers. Although its etiology remains unclear, it is thought that both genetic …

Introduction The etiology of Behçet's disease (BD) is unknown, but widely considered an
excessive T-cell mediated inflammatory response in a genetically susceptible host. Recent …

Background: Lymphedema (LE) is a frequent complication following breast cancer
treatment. While progress is being made in the identification of phenotypic risk factors for the …

Introduction According to genome wide association (GWA) studies as well as candidate
gene approaches, Behçet's disease (BD) is associated with human leukocyte antigen (HLA) …