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Vascular involvement in Behçet’s disease
Abstract
Introduction Behçet’s disease is a chronic recurrent inflammatory disorder usually affecting many organs. The disease derives its name from Hulusi Behçet,1 a Turkish dermatologist, who in 1936 described the symptomatic triad of oral and genital ulcers, and uveitis. The clinical manifestations include a variety of skin and mucosal lesions, uveitis that may result in blindness, a wide range of central nervous system abnormalities, major vessel disease, musculoskeletal problems, and gastrointestinal symptoms. Patients are usually 20-30 years old at the time of onset of the disease.2
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Cited by
Kural-Seyahi, E., Fresko, I., Seyahi, N., Ozyazgan, Y., Mat, C., Hamuryudan, V., Yurdakul, S., & Yazici, H. (2003) · Medicine · doi:10.1097/00005792-200301000-00006 · Cited by 768
Gender differences in Behçet’s disease associated uveitis
Ucar-Comlekoglu, D., Fox, A., & Sen, H. N. (2014) · Journal of Ophthalmology · doi:10.1155/2014/820710 · Cited by 37
Metadata
- Venue
- Textbook of Peripheral Vascular Interventions
- Publisher
- CRC Press
- Published
- 2008-06-02
- Pages
- 763-768
- OpenAlex
- W4256577359
- Cited by
- 435
- References
- 0
- FWCI
- 180.36
- Type
- book chapter
- Language
- en
- Open access
- closed
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- Vascular involvement in Behçet’s disease. (2008). Textbook of Peripheral Vascular Interventions. https://doi.org/10.3109/9781439801970-100
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
