Although inflammation-induced thrombosis is a well-known entity, its pathogenesis remains
complicated. There are complex interactions between inflammation and hemostasis …

Familial Mediterranean fever (FMF) is the most frequent hereditary inflammatory disease
characterized by self-limited recurrent attacks of fever and serositis. It is transmitted in an …

Behçet's disease (BD) is a recurrent systemic inflammatory disorder of unknown origin
characterized by oral and genital mucous ulcer, uveitis, and skin lesions. Involvement of …

Summary Familial Mediterranean Fever (FMF) is the oldest and the most frequent of all
described hereditary periodic fever syndromes. The populations originating from …

Bechet's disease (BD) is an inflammatory, multi systemic disease with spontaneous
remissions and relapses similar to various autoimmune diseases. BD leads to organ …

Behcet's disease (BD) is a systemic inflammatory disorder with a diverse spectrum of clinical
manifestations including mucocutaneous, ocular, vascular, gastrointestinal, musculoskeletal …

Autoinflammatory diseases area group of clinical conditions other than autoimmune
diseases, characterized by recurrent inflammatory episodes. From apathogenetic point of …

Familial Mediterranean fever (FMF) is an inherited autosomal recessive disorder, ethnically
restricted and commonly found among individuals of Mediterranean descent, caused by …

The identification of the genes and proteins mutated in many of the autoinflammatory
diseases has broadened our understanding of the regulation of inflammation and the …

Because of earlier recognition, aggressive medical treatment, and novel surgical
procedures, the morbidity and mortality of large vessel vasculitis in Behçet disease are …