Results 91 to 100 of about 1,238,132 (184)
New and future perspectives in Behçet's syndrome
The Turkish Journal of GastroenterologyBehçet's syndrome is a variable vessel vasculitis characterized by a diverse range of clinical manifestations resulting from inflammation involving several organs and systems.
Bercemhan Sulu, Gulen Hatemi
doaj
Interdisciplinary Approaches to Diagnostic Analysis in Behcet’s Disease
Journal of Indian Academy of Oral Medicine and RadiologyThe exploration of Behçet’s disease challenges the idea that “the oral cavity reflects systemic diseases.” This chronic systemic vasculitis, characterized by oral and genital ulcers, cutaneous lesions, and multi-organ involvement, poses diagnostic ...
Arun Dev Sharma +3 more
doaj +1 more source
Behcet’s disease (BD) is a variable-vessel vasculitis commonly presenting in early adulthood with painful oral aphthous ulcers, genital ulcers, uveitis, pathergy, and skin lesions.
Anders, Casey +3 more
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Could be serum uric acid a risk factor for thrombosis and/or uveitis in Behcet’s disease?
, 2018 IntroductionSerum uric acid level increases in many inflammatory conditions. Uric acid triggers the vascular inflammation and artery damage, which causes to an increased risk of endothelial dysfunction and atherosclerosis.
Avcı Atıl, Avcı Deniz
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Antioxidant Defense System in Behcet’S Disease [PDF]
, 2015 Behcet’s disease (BD), first described by the Turkish dermatologist Hulusi Behcet in 1937, is characterized by triad of symptoms that include oral aphthous lesions, genital ulcerations and iritis with hypopyon.
Şahin, Mustafa +3 more
core +1 more source
Symptom management in Behcet’s disease
, 2018 Objective: To determine the symptoms experienced by patients diagnosed with Behcet’s Disease and how they cope with them. Methods: The qualitative study was conducted from September 2013 to March 2014 at Ege University Medical Faculty Hospital, Turkey ...
Türeyen A.E., Özel F., Aykar F.S.
core
The Study of Ophthalmologic Involvement in 28 Behcet’s Syndrome Patients
پزشکی بالینی ابن سینا, 2004 Behcet’s syndrome is a generalized vasculitis with unknown cause. Acute recurrent iritis , retinal vasculitis , retinal hemorrhage , macular edema , retinal necrosis , ischemic optic neuropathy and vitritis are the most common ophthalmologic involvement.
Mohammad Masoud Panahi
doaj
A Changed Man: A Rare Case of Behcet’s Disease Autoimmune Encephalitis
Behcet’s disease (BD) is characterized by recurrent oral ulcers with concomitant systemic multi-organ involvement, which may include neurological disease, ocular disease, vascular disease, genital ulcers, skin lesions, and arthritis.
London, Jonathan +5 more
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Journal of International Medical ResearchBehçet’s disease, also known as the oral–ocular–genital syndrome, is a chronic systemic vasculitis characterized by recurrent oral and genital ulcers as well as ocular manifestations such as uveitis and conjunctivitis.
Dou Yuan
doaj +1 more source
Neurological Behcet’s disease with transverse myelitis in an adolescent: A case report
Neurological Behcet’s disease is a rare systemic vasculitis marked by recurrent oral or genital ulcers, eye manifestations of uveitis or retinal vasculitis, and skin lesions.
Jeanine McColl +2 more
core +1 more source