Results 31 to 40 of about 730,915 (232)

Genital ulcerative pyoderma gangrenosum in Behçet′s disease: A case report and review of the literature

Indian Journal of Dermatology, 2015
Behçet′s disease (BD), first described by Hulusi Behcet, is a multisystemic disease characterized by recurrent oral and genital ulcerations, ocular and cutaneous lesions, arthritis and vascular disease.
Pinar Ozuguz, Seval Dogruk Kacar, Vildan Manav, Semsettin Karaca, Fatma Aktepe, Sena Ulu   +5 more
doaj   +1 more source

Fractalkine (CX3CL1) levels in patients with Behcet's disease and Neuro-Behcet's disease [PDF]

, 2012
Objective: The aim of the present study was to assess the role of CX3CL1 in patients with active and inactive Behcet's Disease (BD), Neuro-Behcet's Disease (NBD) and control subjects.
Fidan, Işıl, Öztürk, Banu, Gürer, M. Ali, Bozkurt, Banu, İrkeç, Ceyla, Adışen, Esra, İmir, Turgut, Tekşut, Tuba Kuz   +7 more
core   +1 more source

Relationship between Helicobacter pylori and immune dermatosis [PDF]

Yixue xinzhi zazhi, 2021
Infection with Helicobacter pylori (Hp) can result in imbalance in the immune system in humans. The long-term interaction of immunity between host and bacteria leads to loss of the skin au-toantigen tolerance, leading some immunological dermatoses.
Xin-Yan ZHAO, Hong-Yu REN, Ai-Ping FENG
doaj   +1 more source

Additional file 2: of A metagenomic study of the gut microbiome in Behcetâ s disease

, 2018
Supplementary Figures. (PDF 975 kb)
Ye, Zi, Zhang, Ni, Wu, Chunyan, Zhang, Xinyuan, Wang, Qingfeng, Huang, Xinyue, Du, Liping, Cao, Qingfeng, Tang, Jihong, Zhou, Chunjiang, Hou, Shengping, He, Yue, Xu, Qian, Xiong, Xiao, Kijlstra, Aize, Qin, Nan, Yang, Peizeng   +16 more
openaire   +1 more source

Increased CD4(+)CD16(+) and CD4(+)CD56(+) T cell subsets in Behcet's disease [PDF]

, 1999
Behcet's disease is a systemic vasculitis of unknown etiology. Various immune abnormalities have previously been shown in Behcet's disease. We investigated T lymphocyte subsets associated with cytotoxic activity and natural killer (NK) cells by
DİRESKENELİ, RAFİ HANER, ERGUN, SAFİYE ATLAS TÜLİN   +1 more
core   +1 more source

Additional file 1: of Predictors of paravalvular aortic regurgitation after surgery for Behcetâ s disease-related severe aortic regurgitation

, 2019
Figure S1. Schematic diagram showing the selection process of the patient population. Figure S2. Kaplan-Meier estimates of freedom from paravalvular leakage (PVL) stratified by satisfaction of the International Study Group (ISG) criteria. Figure S3. Kaplan-Meier estimates of freedom from paravalvular leakage (PVL) in patients who received postoperative
Choi, Hong-Mi, Kim, Hyung-Kwan, Park, Sung-Ji, Lee, Hyun-Jung, Yoon, Yeonyee, Park, Jun-Bean, Kim, Yong-Jin, Cho, Goo-Young, Hwang, In-Chang, Sohn, Dae-Won, Oh, Jae   +10 more
openaire   +1 more source

HSP 60 expression in mucocutaneous lesions of Behcet's disease [PDF]

, 2001
Background: Heat shock protein (60 kd HSP) has been implicated in the etiology of Behcet's disease, but its expression at sites of inflammation is unknown. Objective: Our aim was to investigate local HSP 60 expression and to quantify T-cell receptor
DİRESKENELİ, RAFİ HANER, ERGUN, SAFİYE ATLAS TÜLİN   +1 more
core   +1 more source

Ocular manifestations of Behcet′s disease in Indian patients.

Indian Journal of Ophthalmology, 2004
Salman Amjad, Parmar Pragya
doaj   +1 more source

Identification of novel genetic susceptibility loci for Behcet's disease using a genome-wide association study [PDF]

, 2009
Introduction Behcet's disease is a chronic systemic inflammatory disease that remains incompletely understood. Herein, we perform the first genome-wide association study in Behcet's disease.
DİRESKENELİ, RAFİ HANER
core   +1 more source

Behcet disease: New aspects [PDF]

, 2017
Behcet disease is currently considered an "autoinfiammatory disease" triggered by infection and environmental factors in genetically predisposed individuals.
Onder, Mettem, Bulur, Isil
core   +1 more source