Vision-Threatening Behcet’s Disease: Severity of Ocular Involvement Predictors
Journal of Ophthalmology, 2018 Purpose. To examine and spot systemic findings commonly associated with a serious form of ocular Behcet’s disease. This could potentially help ophthalmologists categorize their patients based on future risk and plan treatment accordingly.
Mohammed A. Hussein +2 more
doaj +2 more sources
Treatment of Behcet’s disease [PDF]
Chronic Diseases Journal, 2013 Behcet’s disease is a systemic disease classified among vasculitides. Major manifestations are mucous membrane lesions (oral aphthosis and genital aphthosis), skin manifestations (pseudofolliculitis, erythema nodosum), ocular manifestations (uveitis ...
Fereydoun Davatchi +3 more
doaj +2 more sources
Immunosuppressants in Behcet’s disease: a boon or a bane? [PDF]
, 2022 Adalimumab is a disease-modifying antirheumatic drug and monoclonal antibody that works by antagonising tumour necrosis factor-alpha prescribed in many rheumatological conditions like Rheumatic arthritis, Ankylosing spondylitis and Behcet’s disease ...
Shukla, Dhaiwat +3 more
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Retinal S-antigen Th1 cell epitope mapping in patients with Behcet's disease [PDF]
, 2009 Background - Retinal S-antigen (S-Ag) is a most characterized autoantigen of autoimmune uveitis. The recognized immunodominant epitope of human S-Ag in patients with uveitis has not been identified. In this study, we selected certain patients with active
Yang, P.Z. +6 more
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The oral mucosal and salivary microbial community of Behçet's syndrome and recurrent aphthous stomatitis. [PDF]
, 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is ...
Bergmeier, LA +9 more
core +1 more source
The seroprevalence and salivary shedding of herpesviruses in Behcet's syndrome and recurrent aphthous stomatitis [PDF]
, 2015 This journal is published under the terms of the Creative Commons Attribution-NonCommercial 4.0 Unported ...
Bergmeier, LA +9 more
core +1 more source
Bilateral Hemophthalmus — the First Symptom of Behcet’s Disease (Clinical Case) [PDF]
, 2016 Behcet’s disease (BD) — a systemic chronic idiopathic inflammatory recurrent disease of unknown etiology. The development of the disease involve a combination of various factors, among them the most important is genetic and infectious.
E. N. Panina +5 more
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The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome
Leukemia Research Reports, 2020 A relationship has been reported between myelodysplastic syndrome (MDS) and autoimmune disease. Behçet's disease is a multisystem inflammatory disorder with mucocutaneous, articular, gastrointestinal, neurological, and vascular manifestations.
Satoko Oka, Kazuo Ono, Masaharu Nohgawa
doaj +1 more source
Behcet’s Disease in Southeast Asia. Clinical Features, Genetic Study, and Review of Recent Treatment
Journal of Clinical Rheumatology and Immunology, 2021 Behçet’s disease (BD) is a chronic systemic inflammatory disorder characterized by recurrent oral and genital ulcers, skin lesions, and ocular inflammations.
Worawit Louthrenoo
doaj +1 more source
Low Level Laser Therapy to Reduce Recurrent Oral Ulcers in Behçet’s Disease
Case Reports in Dentistry, 2016 Behçet’s disease (BD) is a chronic, relapsing multisystemic vascular condition. Behçet’s disease was described by Hulusi Behçet in 1937. This rare multisystem relapsing-remitting inflammatory disease is poorly understood but is thought to be an ...
D. B. Gandhi Babu +4 more
doaj +1 more source