|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
6
|
|
pubmed:dateCreated |
2010-12-7
|
|
pubmed:abstractText |
Stevens-Johnson syndrome (SJS) and its severe variant, toxic epidermal necrolysis (TEN), are acute inflammatory vesiculobullous reactions of the skin and mucosa. They often affect the ocular surface and can result in permanent visual dysfunction.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Dec
|
|
pubmed:issn |
1097-6825
|
|
pubmed:author |
pubmed-author:FuwaMasahiroM,
pubmed-author:InatomiTsutomuT,
pubmed-author:KinoshitaShigeruS,
pubmed-author:NakanoMasakazuM,
pubmed-author:SotozonoChieC,
pubmed-author:TaniguchiTakazumiT,
pubmed-author:TashiroKeiK,
pubmed-author:TokudaYuichiY,
pubmed-author:UetaMayumiM,
pubmed-author:YagiTomohitoT,
pubmed-author:YokoiNorihikoN
|
|
pubmed:copyrightInfo |
Copyright © 2010 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
126
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1218-25.e10
|
|
pubmed:meshHeading |
pubmed-meshheading:20947153-Cell Line,
pubmed-meshheading:20947153-Conjunctiva,
pubmed-meshheading:20947153-Cytokines,
pubmed-meshheading:20947153-DNA Mutational Analysis,
pubmed-meshheading:20947153-Dinoprostone,
pubmed-meshheading:20947153-Epithelial Cells,
pubmed-meshheading:20947153-Gene Frequency,
pubmed-meshheading:20947153-Genetic Predisposition to Disease,
pubmed-meshheading:20947153-Genome-Wide Association Study,
pubmed-meshheading:20947153-Genotype,
pubmed-meshheading:20947153-Humans,
pubmed-meshheading:20947153-Inflammation,
pubmed-meshheading:20947153-Polymorphism, Genetic,
pubmed-meshheading:20947153-Receptors, Prostaglandin E, EP3 Subtype,
pubmed-meshheading:20947153-Stevens-Johnson Syndrome
|
|
pubmed:year |
2010
|
|
pubmed:articleTitle |
Association between prostaglandin E receptor 3 polymorphisms and Stevens-Johnson syndrome identified by means of a genome-wide association study.
|
|
pubmed:affiliation |
Department of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
