Adamantiades-Behçet's disease is a universal disorder with varying prevalence, ie 80-370
patients per 100,000 inhabitants in Turkey, 2-30 patients per 100,000 inhabitants in Asia …

The German Registry of Adamantiades-BehÇet's disease was founded in 1990 in Berlin and
it provides current data on the epidemiology, the clinical manifestations and the course of …

Abstract Background and Objective: Adamantiades-Behçet disease is a rare entity at a
juvenile age. We aimed to enlighten epidemiological and clinical characteristics of juvenile …

In his third book of “Epidimion” Hippocrates of Kos (460–377 BC) described a disease with
symptoms comparable to the cardinal symptoms of Adamantiades-Behçet disease …

Objectives. To examine the onset signs, clinical cours e, p rog nosis, t re at ment and
outcome of A damantiades-B ehç et's disease in adult Greek pat ients during a 10-year …

Background: Interleukin 8 (IL-8) has recently been under focused investigation because of
its possible participation in the evolution of Adamantiades-Behçet's disease. Objective: The …

Abstract The aetiology of Adamantiades-Behçet's disease remains unknown and its
pathogenesis is not fully understood. Linked intrinsic and extrinsic factors are thought to …

Objective. We investigated the effect of gender on the clinical Adamantiades–Behçet's
disease (ABD) phenotype with data from the German ABD registry and a meta-analysis from …

Behçet's disease (BD) is a systemic vasculitis disorder of unknown etiology, characterized
by relapsing episodes of oral aphthous ulcers, genital ulcers, skin lesions and ocular …

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 …