Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2008-4-1
pubmed:abstractText
To assess in patients followed in a French referral center the clinical spectrum of Vogt-Koyanagi-Harada (VKH) disease and the HLA-DRB1*04 genotype.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1744-5078
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3-8
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:18379934-Adult, pubmed-meshheading:18379934-Alleles, pubmed-meshheading:18379934-Cohort Studies, pubmed-meshheading:18379934-Cross-Sectional Studies, pubmed-meshheading:18379934-Europe, pubmed-meshheading:18379934-European Continental Ancestry Group, pubmed-meshheading:18379934-Female, pubmed-meshheading:18379934-Genotype, pubmed-meshheading:18379934-HLA-DR Antigens, pubmed-meshheading:18379934-HLA-DRB1 Chains, pubmed-meshheading:18379934-Hispanic Americans, pubmed-meshheading:18379934-Humans, pubmed-meshheading:18379934-Male, pubmed-meshheading:18379934-Mediterranean Region, pubmed-meshheading:18379934-Middle Aged, pubmed-meshheading:18379934-Nervous System Diseases, pubmed-meshheading:18379934-Retrospective Studies, pubmed-meshheading:18379934-Skin Diseases, pubmed-meshheading:18379934-Uveomeningoencephalitic Syndrome
pubmed:articleTitle
Characteristics of Vogt-Koyanagi-Harada disease in a French cohort: ethnicity, systemic manifestations, and HLA genotype data.
pubmed:affiliation
Service de Médecine Interne, Laboratoire de recherche clinique et thérapeutique UPRES EA3409, Université Paris XIII, Faculté Léonard de Vinci, Hôpital Avicenne, Assistance Publique-Hôpitaux de Paris, Paris, France. sebastien.abad@avc.ap-hop-paris.fr
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't