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: 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 …

[HTML][HTML] Immunopathogenesis of Behçet's disease and treatment modalities

TB Van der Houwen, PM van Hagen… - Seminars in Arthritis and …, 2022 - Elsevier
Introduction Behçet's disease (BD) is an auto-inflammatory disease, primarily characterized
by recurrent painful mucocutaneous ulcerations. Methods A literature search was performed …

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 …

Understanding Behçet's disease in the context of innate immunity activation

SF Perazzio, LEC Andrade, AWS De Souza - Frontiers in immunology, 2020 - frontiersin.org
Behçet´ s disease (BD) is a heterogeneous condition consisting of idiopathic systemic
vasculitis affecting large and small blood vessels of different types (ie, arteries, veins, or …

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 …

Pathogenesis of Behçet's syndrome: genetic, environmental and immunological factors

I Mattioli, A Bettiol, G Saruhan-Direskeneli… - Frontiers in …, 2021 - frontiersin.org
Behçet's syndrome (BS) is a rare systemic vasculitis, characterized by a wide range of
different clinical involvements and unpredictable phases of recurrence and remission. BS …

[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 …

Behçet's disease: An immunogenetic perspective

A Salmaninejad, MR Zamani… - Journal of Cellular …, 2019 - Wiley Online Library
Behçet's disease (BD) is a chronic and rare multisystemic disorder defined by autoimmunity
and inflammatory characteristics, manifested by ocular lesions, recurrent genital and oral …

[HTML][HTML] Behcet's disease

JR Nair, RJ Moots - Clinical medicine, 2017 - Elsevier
Behçet's disease (BD) is a chronic relapsing and remitting vasculitis of unknown aetiology. It
has the capacity to affect almost all organ systems because of its potential to involve both …