Behçet disease is an idiopathic, multisystem, chronic, and recurrent disease characterized
by exacerbations alternating with phases of quiescence, episodic panuveitis, and …

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 …

Behçet syndrome : Current Opinion in Rheumatology Behçet syndrome : Current Opinion in
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Behçet's disease (BD) is a multisystemic inflammatory disorder. Although the cause and
pathogenesis of BD are still unclear, there is evidence for genetic, immunologic and …

OBJECTIVES Increased homocysteine contributes to the pathophysiology of several chronic
inflammatory diseases. Whether homocysteine could participate in mucosal inflammation in …

The past year has seen some notable publications in the field of vasculitis epidemiology.
The appearance of reports from several different parts of the world has permitted …

Moderate hyperhomocysteinemia is associated with an increased risk of atherosclerosis,
thrombosis and neurodegenerative diseases. Homocysteine accumulation in the blood can …

Behcet's disease (BD) is the only systemic vasculitis involving both arteries and vein in any
sizes. It frequently encounters in rheumatology clinics. It has some major morbidities and …

Behcet's disease (BD) is a multisystemic inflammatory disorder of unknown etiology that is
sometimes associated with thrombosis in addition to systemic manifestations. However, the …

Background Pigmentary dilution is observed in patients with homocystinuria. Therefore, it is
possible that an increase of local homocysteine (Hcy) interferes with normal melanogenesis …