Results 21 to 30 of about 10,530,094 (182)

Could Mean Platelet Volume Be Used as A Marker for Oral Aphthae and Activity of Behçet’s Disease?

open access: yesİstanbul Medical Journal, 2016
Objective: Behçet’s disease is a common inflammatory disease in our country. We aimed to determine whether mean platelet volume can be used as a marker for oral aphthae and the activity of Behçet’s disease.Methods: Between 04/01/2010 and 30/07/2010, 78 ...
Okan Dikker   +5 more
doaj   +1 more source

The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome

open access: yesLeukemia 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

Immunopathogenesis of Behcet's Disease

open access: yesFrontiers in Immunology, 2019
Behcet's disease (BD) is a chronic systemic inflammatory vasculitis of unknown etiology characterized by recurrent episodes of oral aphthous ulcers, genital ulcers, skin lesions, ocular lesions, and other manifestations.
Bainan Tong   +3 more
semanticscholar   +1 more source

Low Level Laser Therapy to Reduce Recurrent Oral Ulcers in Behçet’s Disease

open access: yesCase 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

Regarding neutrophil and lymphocyte responses to oralStreptococcusin Adamantiades–Behçet's disease [PDF]

open access: yesFEMS Immunology & Medical Microbiology, 2006
Dear Editor, I read the recent study of Kurauchi et al. entitled ‘Neutrophil and lymphocyte responses to oral Streptococcus in Adamantiades–Behcet's disease’ ( FEMS Immunol Med Microbiol 43: 125–131) with great interest. The authors evaluated neutrophil reactions and cytokine production levels by lymphocytes after stimulation with Streptococcus ...
openaire   +2 more sources

Behçet's Disease (Adamantiades-Behçet's Disease)

open access: yesClinical and Developmental Immunology, 2011
Adamantiades-Behçet's disease (ABD) is characterized by starting with oral aphthous ulceration and developing of the systemic involvements. The pathogenesis of ABD is closely correlated with the genetic factors and the triggering factors which acquire ...
Fumio Kaneko   +7 more
doaj   +1 more source

Budd-Chiari syndrome in a 25-year-old woman with Behçet's disease: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2011
Introduction The risk that patients with Behçet's disease will develop thrombotic complications has been previously described. Although it is distributed worldwide, Behçet's disease is rare in the Americas and Europe.
Évora Paulo RB   +4 more
doaj   +1 more source

Behçet’s Disease: An Overview of Etiopathogenesis

open access: yesFrontiers in Immunology, 2019
Behçet's disease (BD) is a systemic inflammatory disease with a chronic, relapsing-remitting course of unknown etiology hallmarked predominantly by mucocutaneous lesions and ocular involvement.
P. Leccese, E. Alpsoy
semanticscholar   +1 more source

Common genetic susceptibility loci link PFAPA syndrome, Behçet’s disease, and recurrent aphthous stomatitis

open access: yesProceedings of the National Academy of Sciences of the United States of America, 2020
Significance In this report we identify genetic susceptibility variants for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome, the most common periodic fever syndrome in children.
K. Manthiram   +29 more
semanticscholar   +1 more source

A metagenomic study of the gut microbiome in Behcet’s disease

open access: yesMicrobiome, 2018
Behcet’s disease (BD) is a recalcitrant, multisystemic inflammatory disease that can lead to irreversible blindness. Microbial agents have been considered to contribute to the pathogenesis of this disease, but the underlying mechanisms remain unclear. In
Z. Ye   +16 more
semanticscholar   +1 more source

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