Behçet′ s disease (BD) is a systemic inflammatory disorder characterized mainly by
recurrent oral and genital ulcers and eye involvement. Although the pathogenesis remains …

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

Behçet disease is a multi-system disease associated with human leukocyte antigen (HLA)
class I polymorphism. High-resolution next-generation sequencing (NGS) with haplotype …

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

Objectives. To analyze demographic, clinical and genetic features of Behçet's disease (BD)
in Tunisia and to'compare them with other ethnic and geographic groups. Methods. Two …

Behçet's disease (BD) is a multifactorial disease with a strong genetic background. Higher
frequencies of patients with a positive family history for BD were reported from the Middle …

Behcet syndrome (BS) is a multisystemic perivasculitis whose genetic susceptibility is linked
to HLA region. We first meta‐analysed all HLA class I and II genes involved in BS …

Behçet's disease is a genetically complex disease of unknown etiology characterized by
recurrent inflammatory attacks affecting the orogenital mucosa, eyes and skin. We performed …

Objective. To review the progress in the field of MHC-related genetic susceptibility to
Behçet's disease (BD). Method. Systematic review of the English literature between 1 …

Objective. To define the contribution of HLA genes and extended HLA haplotypes to the
susceptibility to Behçet's disease (BD) in Sardinia. Methods. Forty-five unrelated Sardinian …