Risk factors, clinical features and treatment of Behçet's disease uveitis

Z Zhong, G Su, P Yang - Progress in Retinal and Eye Research, 2023 - Elsevier
Behçet's disease is a systemic vasculitis frequently associated with intraocular inflammation.
Recent findings identified independent clinical clusters in Behçet's disease, each involving …

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 …

2018 update of the EULAR recommendations for the management of Behçet's syndrome

G Hatemi, R Christensen, D Bang, B Bodaghi… - Annals of the …, 2018 - ard.bmj.com
Several new treatment modalities with different mechanisms of action have been studied in
patients with Behçet's syndrome (BS). The aim of the current effort was to update the …

[HTML][HTML] Diagnosis and management of Neuro-Behçet's disease: international consensus recommendations

S Kalra, A Silman, G Akman-Demir, S Bohlega… - Journal of …, 2014 - Springer
Neuro-Behçet's disease (NBD) is one of the more serious manifestations of Behçet's disease
(BD), which is a relapsing inflammatory multisystem disease with an interesting …

Neuro-Behçet's disease: epidemiology, clinical characteristics, and management

A Al-Araji, DP Kidd - The Lancet Neurology, 2009 - thelancet.com
Behçet's disease (BD) is a multisystem relapsing inflammatory disorder of unknown cause.
In neuro-BD (NBD), the CNS can be involved in one or both of two ways: first, and most …

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 …

Neutrophilic dermatoses: pathogenesis, Sweet syndrome, neutrophilic eccrine hidradenitis, and Behçet disease

CA Nelson, S Stephen, HJ Ashchyan… - Journal of the American …, 2018 - Elsevier
Neutrophilic dermatoses are a heterogeneous group of inflammatory skin disorders that
present with unique clinical features but are unified by the presence of a sterile …

Efficacy of anti-TNF alpha in severe and/or refractory Behçet's disease: multicenter study of 124 patients

H Vallet, S Riviere, A Sanna, A Deroux, G Moulis… - Journal of …, 2015 - Elsevier
Objective To report the efficacy and safety of anti-TNF agents in patients with severe and/or
refractory manifestations of Behçet's disease (BD). Methods We performed a multicenter …

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 …

[HTML][HTML] Gastrointestinal Behçet's disease: a review

W Skef, MJ Hamilton, T Arayssi - World Journal of …, 2015 - ncbi.nlm.nih.gov
Behçet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic vasculitis
characterized by recurrent oral and genital aphthous ulcers, ocular disease and skin lesions …