about
Behçet's disease: from Hippocrates to the third millenniumBehçet's disease in children, an overviewThe immunogenetics of Behçet's disease: A comprehensive reviewIdentification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association studyCausal attributions about disease onset and relapse in patients with systemic vasculitis.Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.Histopathological Evaluation of Behçet's Disease and Identification of New Skin LesionsPulmonary manifestations of Behçet's diseaseBehçet's disease: infectious aetiology, new autoantigens, and HLA-B51Associations between the HLA-A polymorphism and the clinical manifestations of Behcet's diseaseGenome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease.A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease.NOD2 is highly expressed in Behçet disease with pulmonary manifestations.Behçet's disease: a review.Polymorphisms of Promoter Region of TNF-α Gene in Iranian Azeri Turkish Patients with Behçet's DiseaseBehçet's disease physiopathology: a contemporary review.Ear, nose and throat manifestations of Behçet's disease: a review.Managing Behçet's disease: An update on current and emerging treatment options.Do clinical findings of Behçet's disease vary by gender?: A single-center experience from 329 patients.HLA-B*51 and Behçet Disease.Behçet syndrome: is it one condition?Ocular manifestations of the autoinflammatory syndromes.Pathogenesis of Behçet's disease: autoinflammatory features and beyond.Behçet's disease: A comprehensive review with a focus on epidemiology, etiology and clinical features, and management of mucocutaneous lesions.Genetics and immunodysfunction underlying Behçet's disease and immunomodulant treatment approaches.Behçet's syndrome: providing integrated care.On the genetics of the Silk Route: association analysis of HLA, IL10, and IL23R-IL12RB2 regions with Behçet's disease in an Iranian population.Evaluation of KIR3DL1/KIR3DS1 polymorphism in Behçet's disease.Intestinal and neurological involvement in Behcet disease: a clinical case.Knitting the Threads of Silk through Time: Behçet's Disease-Past, Present, and FutureGenetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese.Interleukin-4 gene polymorphisms confer Behçet's disease in Turkish population.Genetic variant on PDGFRL associated with Behçet disease in Chinese Han populations.Is Behçet's disease a 'class 1-opathy'? The role of HLA-B*51 in the pathogenesis of Behçet's disease.Association of killer cell immunoglobulin-like receptor (KIR) genes and their HLA ligands with susceptibility to Behçet's disease.Demographic and clinical features of Behcet's disease in Azerbaijan.Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis.Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182.Genetics of Behçet's Disease.Behçet's disease
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Familial aggregation of Behçet's disease in Turkey.
@ast
Familial aggregation of Behçet's disease in Turkey.
@en
Familial aggregation of Behçet's disease in Turkey.
@nl
type
label
Familial aggregation of Behçet's disease in Turkey.
@ast
Familial aggregation of Behçet's disease in Turkey.
@en
Familial aggregation of Behçet's disease in Turkey.
@nl
prefLabel
Familial aggregation of Behçet's disease in Turkey.
@ast
Familial aggregation of Behçet's disease in Turkey.
@en
Familial aggregation of Behçet's disease in Turkey.
@nl
P2093
P2860
P356
P1476
Familial aggregation of Behçet's disease in Turkey.
@en
P2093
P2860
P304
P356
10.1136/ARD.59.8.622
P407
P577
2000-08-01T00:00:00Z