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

Abstract Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disorder
characterised by acute attacks of fever and serosal inflammation. FMF primarily affects …

Objectives FMF is the most common periodic fever syndrome, characterized by recurrent
episodes of fever and serosal inflammation accompanied with high acute phase reactants …

Mutations in the MEFV gene, which encodes the protein named pyrin (also called
marenostrin or TRIM20), are associated with the autoinflammatory disease familial …

Familial Mediterranean fever (FMF) is characterized by recurrent short-lived/self-limiting
inflammatory attacks. Besides these, a substantial number of patients with FMF present with …

Monogenic autoinflammatory syndromes (MAISs) are caused by innate immune system
dysregulation leading to aberrant inflammasome activation and episodes of fever and …

Introduction: Colchicine has been successfully used for the treatment of neutrophilic
disorders such as familial Mediterranean fever (FMF), Behçet disease (BD) and gout. There …

Familial Mediterranean fever (FMF) is A common periodic fever syndrome. The causative
gene of the FMF is named Mediterranean Fever gene (MEFV). Increased inflammation in …

Certain types of vasculitis occur more frequently and present differently in patients with
familial Mediterranean fever (FMF). We assessed the characteristics of patients with FMF …

Polyarteritis nodosa (PAN) is a rare form of primary systemic vasculitis with heterogeneous
presentations, treatments and disease course. Historical approaches to classification and …