Global epidemiology of vasculitis

RA Watts, G Hatemi, JC Burns… - Nature reviews …, 2022 - nature.com
The many forms of vasculitis are characterized by inflammation of blood vessels, leading to
potentially long-term sequelae including vision loss, aneurysm formation and kidney failure …

IL-1 and autoinflammatory disease: biology, pathogenesis and therapeutic targeting

L Broderick, HM Hoffman - Nature Reviews Rheumatology, 2022 - nature.com
Over 20 years ago, it was first proposed that autoinflammation underpins a handful of rare
monogenic disorders characterized by recurrent fever and systemic inflammation. The …

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 …

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 Syndrome

D Saadoun, B Bodaghi, P Cacoub - New England Journal of …, 2024 - Mass Medical Soc
Behçet’s Syndrome | New England Journal of Medicine Skip to main content Access provided
byKuopion Yliopistollinen Sairaala The New England Journal of Medicine homepage Advanced …

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1

Y Kirino, G Bertsias, Y Ishigatsubo, N Mizuki… - Nature …, 2013 - nature.com
Individuals with Behçet's disease suffer from episodic inflammation often affecting the
orogenital mucosa, skin and eyes. To discover new susceptibility loci for Behçet's disease …

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 …

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 …