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Diagnosing neuro-Behçet’s disease [PDF]
Romanian Journal of Neurology, 2021 Behçet’s disease is a rare systemic vasculitis characterized by uveitis, recurrent oral and genital ulcers, firstly described by the turkish dermatologist Hulusi Behçet. The etiology is unknown, although autoimmune mechanisms are described.
Catalina Elena Bistriceanu +2 more
doaj +1 more source
Clinical Medicine, 2017 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 arteries and veins of all sizes, resulting in significant organ-threatening morbidity and mortality.
Nair, Jagdish R, Moots, Robert J
openaire +4 more sources
Uveitis and Retinal Vasculitis—Harbingers of Neuro-Behcet’s Disease: A Case Report [PDF]
Bengal Physician Journal, 2023 We report this case of Neuro-Behcet’s disease who initially had recurrent episodes of uveitis over a period of 14 years and was under ophthalmological follow-up. Recently, she developed retinal vasculitis and multiple stroke-like episodes.
Pramod Kumar Samala +6 more
doaj +1 more source
Gazi Medical Journal, 2019 Behcet's Disease (BD) was first described by Hulusi Behcet in 1937 as a disease characterized by recurrent aphthous ulceration in the mouth and genital area and hypopyon iridocyclitis. Diagnostic criteria developed by the International Working Group in 1990 were generally accepted among dermatologists.
ADIŞEN, ESRA, Temel, Berkay
+8 more sources
Genetics of Behçet's Disease: Functional Genetic Analysis and Estimating Disease Heritability
Frontiers in Medicine, 2021 Behçet's disease is a chronic multisystemic inflammatory disorder characterized by recurrent oral and genital ulcers. Although its etiology remains unclear, it is thought that both genetic and environmental factors contribute to the onset and progression
Lourdes Ortiz-Fernández +4 more
doaj +1 more source
Evaluation of disease activity in uveoretinitis associated with Behçet’s disease
Immunological Medicine, 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
doaj +1 more source
Cerebral pseudotumoral form of Behçet’s disease: About 3 cases
Interdisciplinary Neurosurgery, 2020 Behçet’s disease is a multisystem vasculitis which can involve the nervous system known as Neuro-Behçet’s disease. Neurological involvement is uncommon in Behçet’s disease, and has a highly variable prevalence.
Malek Mansour +4 more
doaj +1 more source
Clinical and Experimental Medicine, 2004 Behcet's disease (BD) is a systemic disorder of recurrent acute inflammation, characterized by major symptoms of oral aphthous ulcers, uveitis, skin lesions and genital ulcers. Involvement of intestines, vessels, and central nervous system (CNS) sometimes leads to a poor prognosis.
M, Suzuki Kurokawa, N, Suzuki
+7 more sources
Blepharoptosis in Behçet's Disease [PDF]
Archives of Aesthetic Plastic Surgery, 2016 Behçet's disease is a systemic chronic disease that occurs in tissues such as eyes, joints, organs and nerves, and it has been noted that symptoms may be observed in a variety of tissues.
So-Min Hwang +4 more
doaj +1 more source
eComment. Behcet's disease or Adamantiades-Behcet's disease? [PDF]
Interactive CardioVascular and Thoracic Surgery, 2012 Memetoglu and Kalkan, in their well-written manuscript have reported on the successful percutaneous treatment of an aneurysm in a patient with Behcet's disease [1]. We agree with the consideration of a percutaneous therapeutic modality instead of conventional surgical treatment for the management of aneurysms in Behcet's disease and would like to add a
Georgios, Dimitrakakis +1 more
openaire +2 more sources