Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
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Vogt-Koyanagi-Harada disease: review of a rare autoimmune disease targeting antigens of melanocytesVogt-Koyanagi-Harada syndrome - current perspectives.FGFR1OP tagSNP but not CCR6 polymorphisms are associated with Vogt-Koyanagi-Harada syndrome in Chinese HanCharacteristics of Vogt-Koyanagi-Harada disease in a French cohort: ethnicity, systemic manifestations, and HLA genotype data.A functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis.Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndromeHypermethylation of Interferon Regulatory Factor 8 (IRF8) Confers Risk to Vogt-Koyanagi-Harada DiseaseFrequency of distinguishing clinical features in Vogt-Koyanagi-Harada diseaseThe Association of Chemokine Gene Polymorphisms with VKH and Behcet's Disease in a Chinese Han Population.Vogt-Koyanagi-Harada disease in an 8-year-old boyAssociation of HLA-DR4/HLA-DRB1*04 with Vogt-Koyanagi-Harada disease: a systematic review and meta-analysis.Characteristics of uveitic glaucoma and evaluation of its surgical treatmentTNFAIP3 gene polymorphisms in a Chinese Han population with Vogt-Koyanagi-Harada syndrome.Decreased 1,25-Dihydroxyvitamin D3 level is involved in the pathogenesis of Vogt-Koyanagi-Harada (VKH) disease.Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han populationThe role of sex in uveitis and ocular inflammation.Correlation between Retinal Changes and Visual Function in Late-Stage Vogt-Koyanagi-Harada Disease: An Optical Coherence Tomography Study.Laser flare-cell photometer: principle and significance in clinical and basic ophthalmology.Comparison of the Clinical Manifestations between Acute Vogt-Koyanagi-Harada Disease and Acute Bilateral Central Serous Chorioretinopathy.miR-23a, miR-146a and miR-301a confer predisposition to Vogt-Koyanagi-Harada syndrome but not to Behcet's disease.Reversible alopecia in Vogt-Koyanagi-Harada disease and sympathetic ophthalmiaAssociation of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population.PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndromePolymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndromeMonocyte chemoattractant protein (MCP)-1 -2518 A/G SNP in Chinese Han patients with VKH syndromeGenetic analysis of innate immunity in Behcet's disease identifies an association with IL-37 and IL-18RAP.Two cases of Vogt-Koyanagi-Harada's disease in sub-Saharan AfricaAssociation of TNFSF4 Polymorphisms with Vogt-Koyanagi-Harada and Behcet's Disease in Han Chinese.Distinguishing features of acute Vogt-Koyanagi-Harada disease and acute central serous chorioretinopathy on optical coherence tomography angiography and en face optical coherence tomography imaging.Clinical Outcomes of Patients with Vogt-Koyanagi-Harada Disease Over 12 Years at a Tertiary Center.Incidence and Risk Factors for Developing Glaucoma Among Patients with Uveitis in a University-based Tertiary Referral Center in Riyadh, Saudi Arabia.Surgical Treatment of Subretinal Fibrosis Caused Macular Detachment in Vogt-Koyanagi-Harada Disease: A Pioneer Study.Reappraisal of the management of Vogt-Koyanagi-Harada disease: sunset glow fundus is no more a fatality.The spectrum of Vogt-Koyanagi-Harada disease in Iran.Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility.Outcomes of Vogt-Koyanagi-Harada Disease: A Subanalysis From a Randomized Clinical Trial of Antimetabolite TherapiesInvestigation of the association of Vogt-Koyanagi-Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai.TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behçet's disease and Vogt-Koyanagi-Harada syndrome: a case-control study.
P2860
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P2860
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@ast
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@en
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@nl
type
label
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@ast
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@en
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@nl
prefLabel
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@ast
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@en
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@nl
P2093
P1433
P1476
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients.
@en
P2093
P304
P356
10.1016/J.OPHTHA.2006.07.040
P577
2006-11-21T00:00:00Z