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Page 1
Behcet disease: New aspects.
Bulur I, Onder M. Bulur I, et al. Clin Dermatol. 2017 Sep-Oct;35(5):421-434. doi: 10.1016/j.clindermatol.2017.06.004. Epub 2017 Jun 27. Clin Dermatol. 2017. PMID: 28916023 Review.
Behcet disease is currently considered an "autoinflammatory disease" triggered by infection and environmental factors in genetically predisposed individuals. ...It is important to evaluate the patient with complex aphthosis for Behcet disease an …
Behcet disease is currently considered an "autoinflammatory disease" triggered by infection and environmental factors i …
Gastrointestinal Behcet's disease: a review.
Skef W, Hamilton MJ, Arayssi T. Skef W, et al. World J Gastroenterol. 2015 Apr 7;21(13):3801-12. doi: 10.3748/wjg.v21.i13.3801. World J Gastroenterol. 2015. PMID: 25852265 Free PMC article. Review.
Behcet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic vasculitis characterized by recurrent oral and genital aphthous ulcers, ocular disease and skin lesions. ...By comparison, the prevalence in North American and Northern European countr …
Behcet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic vasculitis characterized by recurrent oral and geni …
Immunopathogenesis of Behcet Disease.
Nieto IG, Alabau JLC. Nieto IG, et al. Curr Rheumatol Rev. 2020;16(1):12-20. doi: 10.2174/1573397115666190415142426. Curr Rheumatol Rev. 2020. PMID: 30987569 Review.
BACKGROUND: Behcet's Disease (BD, OMIM 109650) is a chronic relapsing inflammatory disease of unknown etiology with unpredictable exacerbations and remissions. First described in 1937 by the Turkish dermatologist HulusiBehcet, as a trisympton complex (oral an …
BACKGROUND: Behcet's Disease (BD, OMIM 109650) is a chronic relapsing inflammatory disease of unknown etiology with unp …
Classification Criteria for Behcet Disease Uveitis.
Standardization of Uveitis Nomenclature (SUN) Working Group. Standardization of Uveitis Nomenclature (SUN) Working Group. Am J Ophthalmol. 2021 Aug;228:80-88. doi: 10.1016/j.ajo.2021.03.058. Epub 2021 May 11. Am J Ophthalmol. 2021. PMID: 33845008 Free PMC article.
PURPOSE: To determine classification criteria for Behcet disease uveitis. DESIGN: Machine learning of cases with Behcet disease and 5 other panuveitides. ...Key criteria for Behcet disease uveitis were a diagnosis of Behcet dise …
PURPOSE: To determine classification criteria for Behcet disease uveitis. DESIGN: Machine learning of cases with Behcet …
Behcet disease: an undifferentiating and complex vasculitis.
Pak D, Park HJ. Pak D, et al. Postgrad Med. 2023 Jan;135(sup1):33-43. doi: 10.1080/00325481.2022.2159205. Epub 2022 Dec 29. Postgrad Med. 2023. PMID: 36533384 Review.
Behcet Disease is a relapsing and remitting variable vessel vasculitis characterized by recurrent mucocutaneous ulcers that can involve almost every organ system in the body. Indeed, the presence of recurrent oral or genital ulcers with other auto-inflammatory sympt …
Behcet Disease is a relapsing and remitting variable vessel vasculitis characterized by recurrent mucocutaneous ulcers that ca …
Neuro-Behcet's disease: A review.
Belfeki N, Ghriss N, Fourati M, Leclercq D, Saadoun D. Belfeki N, et al. Rev Med Interne. 2024 Oct;45(10):624-633. doi: 10.1016/j.revmed.2024.06.007. Epub 2024 Jun 26. Rev Med Interne. 2024. PMID: 38937151 Review.
Behcet disease (BD) is a systemic vasculitis which can involve many different organ systems. ...
Behcet disease (BD) is a systemic vasculitis which can involve many different organ systems. ...
Behcet's disease.
Saadoun D, Wechsler B. Saadoun D, et al. Orphanet J Rare Dis. 2012 Apr 12;7:20. doi: 10.1186/1750-1172-7-20. Orphanet J Rare Dis. 2012. PMID: 22497990 Free PMC article. Review.
DEFINITION OF THE DISEASE: Behcet disease (BD) is a chronic, relapsing, multisystemic disorder characterized by mucocutaneous, ocular, vascular and central nervous system manifestations. ...DIFFERRENTIAL DIAGNOSIS: It depends on the clinical presentation of B …
DEFINITION OF THE DISEASE: Behcet disease (BD) is a chronic, relapsing, multisystemic disorder characterized by mucocut …
Behcet disease, familial Mediterranean fever and MEFV variations: More than just an association.
Seyahi E, Ugurlu S, Amikishiyev S, Gul A. Seyahi E, et al. Clin Immunol. 2023 Jun;251:109630. doi: 10.1016/j.clim.2023.109630. Epub 2023 Apr 30. Clin Immunol. 2023. PMID: 37216220 Review.
Behcet disease (BD) and familial Mediterranean fever (FMF) are two inflammatory disorders that share many features including historical background, ethnical distribution and inflammatory characteristics. ...Whether these variants are associated with certain disea …
Behcet disease (BD) and familial Mediterranean fever (FMF) are two inflammatory disorders that share many features including h …
Behcet's syndrome.
Emmi G, Bettiol A, Hatemi G, Prisco D. Emmi G, et al. Lancet. 2024 Mar 16;403(10431):1093-1108. doi: 10.1016/S0140-6736(23)02629-6. Epub 2024 Feb 22. Lancet. 2024. PMID: 38402885 Review.
Behcet's syndrome is a rare, chronic multisystemic inflammatory disorder also known as the Silk Route disease due to its geographical distribution. Behcet's syndrome is a multifactorial disease and infectious, genetic, epigenetic, and imm …
Behcet's syndrome is a rare, chronic multisystemic inflammatory disorder also known as the Silk Route disease due to it …
Neutrophilic dermatoses: Pathogenesis, Sweet syndrome, neutrophilic eccrine hidradenitis, and Behcet disease.
Nelson CA, Stephen S, Ashchyan HJ, James WD, Micheletti RG, Rosenbach M. Nelson CA, et al. J Am Acad Dermatol. 2018 Dec;79(6):987-1006. doi: 10.1016/j.jaad.2017.11.064. Epub 2018 Apr 11. J Am Acad Dermatol. 2018. PMID: 29653210 Review.
The first article in this continuing medical education series explores the pathogenesis of neutrophilic dermatoses and reviews the epidemiology, clinical and histopathologic features, diagnosis, and management of Sweet syndrome, neutrophilic eccrine hidradenitis, and Be …
The first article in this continuing medical education series explores the pathogenesis of neutrophilic dermatoses and reviews the epidemiol …
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