Behcet's disease: A comprehensive review with a focus on epidemiology, etiology and clinical features, and management of mucocutaneous lesions

E Alpsoy - The Journal of dermatology, 2016 - Wiley Online Library
Behçet's disease (BD) is a chronic, relapsing, inflammatory multisystem disease of unknown
etiology. Oral ulcers, genital ulcers, cutaneous lesions, and ocular and articular involvement …

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 …

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease

EF Remmers, F Cosan, Y Kirino, MJ Ombrello… - Nature …, 2010 - nature.com
Behçet's disease is a genetically complex disease of unknown etiology characterized by
recurrent inflammatory attacks affecting the orogenital mucosa, eyes and skin. We performed …

Behçet's disease physiopathology: a contemporary review

MJ Zeidan, D Saadoun, M Garrido, D Klatzmann… - Autoimmunity …, 2016 - Springer
Behçet's disease, also known as the Silk Road Disease, is a rare systemic vasculitis
disorder of unknown etiology. Recurrent attacks of acute inflammation characterize Behçet's …

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 …

Current concepts in the etiology and treatment of Behçet disease

C Evereklioglu - Survey of ophthalmology, 2005 - Elsevier
Behçet disease is an idiopathic, multisystem, chronic, and recurrent disease characterized
by exacerbations alternating with phases of quiescence, episodic panuveitis, and …

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 …

Behçet's disease: infectious aetiology, new autoantigens, and HLA-B51

H Direskeneli - Annals of the rheumatic diseases, 2001 - ard.bmj.com
Neutrophils are mature immune cells with a very short life in vitro and have a pivotal role in
innate immune responses. As typical BD lesions such as pustular folliculitis, pathergy …

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 …

[PDF][PDF] Behcet's disease: an update on the pathogenesis

A Gul - Clinical and experimental rheumatology, 2001 - clinexprheumatol.org
Behçet's disease is a chronic inflammatory disorder of unknown etiology. It has long been
postulated that immunological abnormalities, which are possibly induced by microbial …