New insights into the pathogenesis of Behcet's disease

MP de Chambrun, B Wechsler, G Geri, P Cacoub… - Autoimmunity …, 2012 - Elsevier
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 …

Immunopathogenesis of Behcet's disease

B Tong, X Liu, J Xiao, G Su - Frontiers in immunology, 2019 - frontiersin.org
Behcet's disease (BD) is a chronic systemic inflammatory vasculitis of unknown etiology
characterized by recurrent episodes of oral aphthous ulcers, genital ulcers, skin lesions …

Behçet's disease: an overview of etiopathogenesis

P Leccese, E Alpsoy - Frontiers in immunology, 2019 - frontiersin.org
Behçet's disease (BD) is a systemic inflammatory disease with a chronic, relapsing-remitting
course of unknown etiology hallmarked predominantly by mucocutaneous lesions and …

Etiopathogenesis of Behçet's disease with emphasison the role of immunological aberrations

VD Kapsimali, MA Kanakis, GA Vaiopoulos… - Clinical …, 2010 - Springer
Behçet's disease (BD) is a chronic multisystemic inflammatory disorder of unknown origin
consisting of oral aphthous ulcers, ocular symptoms, skin lesions, and genital ulcerations. It …

The immunogenetics of Behçet's disease: A comprehensive review

M Takeuchi, DL Kastner, EF Remmers - Journal of autoimmunity, 2015 - Elsevier
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's disease–a contemporary review

D Mendes, M Correia, M Barbedo, T Vaio, M Mota… - Journal of …, 2009 - Elsevier
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 …

Pathogenesis of Behçet's disease: autoinflammatory features and beyond

A Gül - Seminars in immunopathology, 2015 - Springer
Behçet's disease (BD) is an inflammatory disorder of unknown aetiology characterised by
recurrent attacks affecting the mucocutaneous tissues, eyes, joints, blood vessels, brain and …

Behçet's disease

SE Marshall - Best Practice & Research Clinical Rheumatology, 2004 - Elsevier
Behçet's disease is a systemic vasculitis characterized by recurrent oral and genital ulcers,
and ocular inflammation, and which may involve the joints, skin, central nervous system and …

Behçet's disease as an autoinflammatory disorder

A Gul - Current Drug Targets-Inflammation & Allergy, 2005 - ingentaconnect.com
Autoinflammatory diseases are a group of heritable disorders that are characterized by
seemingly unprovoked episodes of inflammation at certain locations and and relative lack of …

[PDF][PDF] Behçet's disease: familial clustering and immunogenetics

P Fietta - Clinical and experimental rheumatology, 2005 - clinexprheumatol.org
Behçet's disease (BD) is a relapsing, multisystemic inflammatory disorder, characterized by
major symptoms consisting of recurrent orogenital ulcerations, eye and skin lesions. Other …