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Carotid artery aneurysm as the initial presentation of Behçet's disease: A case report. [PDF]
J Vasc Surg Cases Innov TechBehçet’s disease is a rare systemic vasculitis that may involve arteries and veins. Carotid artery aneurysms are extremely uncommon and can be the initial manifestation.
Bengrad A +7 more
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Erythema nodosum in Behçet’s disease in remission: Think COVID-19? [PDF]
, 2023 The coronavirus disease has several manifestations related to the activation of the immune system. Because of such activation, autoimmune diseases, including vasculitis, have been reported to occur.
Jawad, Ali S.M. +2 more
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Evaluation of disease activity in uveoretinitis associated with Behçet’s disease
, 2021 Behçet’s disease is a multi-organ inflammatory disorder with systemic vasculitis of unknown etiology. Ocular lesions occur in about 70% of patients with Behçet’s disease, and it is more frequent and severe in men.
Hiroshi Keino
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Ocular lesions in Behçet’s disease
, 2022 Behçet’s disease is a rare systemic vasculitis that involves both arteries and veins of various sizes. The main symptoms of the condition are aphthous mouth ulcers and genital ulcers, skin and ocular lesions, neurological disorders, arthritis and ...
Chmielewski, Grzegorz; Department of Rheumatology, School of Medicine, Collegium Medicum, University of Warmia and Mazury, Olsztyn, Poland +2 more
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Behçet’s disease physiopathology: a contemporary review [PDF]
, 2016 International audienceBehçet’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 disease. Frequent oral aphthous ulcers, genital ulcers,
Klatzmann, David +11 more
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Gender Differences in Behçet’s Disease Associated Uveitis [PDF]
, 2014 Behçet’s disease is a systemic vasculitis of unknown etiology, characterized by oral and genital ulceration, skin lesions, and uveitis as well as vascular, central nervous system, and gastrointestinal system involvement.
Didar Ucar-Comlekoglu +2 more
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Contemporary possibilities of the diagnosis and treatment in Behçet’s disease
, 2022 Behçet’s disease (BD – Behçet’s disease/BS – Behçet’s syndrome) is a chronic, systemic inflammatory vasculitis of unknown etiology, characterized by recurrent episodes of variable vessel vasculitis with heterogenous clinical features.
Kiecana, Aleksander, Kołodziej, Joanna
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Behçet’s Disease and Intracardiac Thrombosis: A Report of Three Cases [PDF]
, 2013 We present three patients with Behçet’s disease associated with intracardiac thrombus and pulmonary vascular involvement. One of these patients had also Budd-Chiari syndrome.
Demet Menekşe Gerede +8 more
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Frenemies within: An Endocarditis Case in Behçet’s Disease
, 2021 A 57-year female patient diagnosed with Behçet’s disease, on azathioprine, was noticed to have at a routine examination antinuclear and antiphospholipid antibodies.
Simona Rednic +7 more
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Neutrophil and lymphocyte responses to oral Streptococcus in Adamantiades-Behcet's disease
, 2005 Immune reactions against microorganisms play an important pathogenic role in Adamantiades-Behçet’s disease (ABD). We had previously obtained Streptococcus sanguinis (strain BD113-20) isolated from the oral cavity of patients with ABD.
Oguma, Keiji +7 more
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