Results 1 to 10 of about 10,427 (115)
Upper Gastrointestinal Involvement in Behcet’s Disease [PDF]
The Korean Journal of GastroenterologyBackground/Aims: Behcet's disease is an idiopathic, chronic, multisystemic vasculitis characterized by recurrent oral and genital ulcers, ophthalmologic inflammation, and skin lesions.
Hogyung Jun +3 more
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Neurological Behcet’s disease with transverse myelitis in an adolescent: A case report [PDF]
SAGE Open Medical Case ReportsNeurological 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
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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
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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
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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
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Long-Term Outcomes of Behçet’s Syndrome-Related Uveitis: A Monocentric Italian Experience
Mediators of Inflammation, 2020 Objectives. To examine demographic and clinical characteristics and long-term visual outcome in a cohort of Italian patients affected by Behçet’s uveitis (BU). Materials and Methods.
Jurgen Sota +9 more
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Real-Life Data on the Efficacy of Canakinumab in Patients with Adult-Onset Still’s Disease
Mediators of Inflammation, 2020 Background. Interleukin-1 inhibition has revealed to be a successful treatment approach for patients with adult-onset Still’s disease (AOSD). However, real-life experience is focused on the use of anakinra, while data about canakinumab (CAN) are mainly ...
Antonio Vitale +12 more
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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
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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
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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