Vogt-Koyanagi-Harada Disease in an Adolescent Boy

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dc.authoridGündüz, Abuzer/0000-0003-1752-6810
dc.authoridBILGIC, OZLEM/0000-0001-9201-8299
dc.authorwosidBİLGİÇ, ÖZLEM/HHS-2451-2022
dc.authorwosidGündüz, Abuzer/HLH-2417-2023
dc.contributor.authorBilgic, Ozlem
dc.contributor.authorGunduz, Abuzer
dc.contributor.authorKaya, Kismet
dc.date.accessioned2024-08-04T20:38:01Z
dc.date.available2024-08-04T20:38:01Z
dc.date.issued2014
dc.departmentİnönü Üniversitesien_US
dc.description.abstractVogt-Koyanagi-Harada (VKH) disease is a rare multiorgan disorder that affects the melanocytes of the eyes, skin, inner ear, and meninges. It is more common in women and in patients 30 to 50 years of age; it is rarely seen in children. We report a 14-year-old boy who meets the criteria for complete VKH disease.en_US
dc.identifier.doi10.1111/pde.12163
dc.identifier.endpage101en_US
dc.identifier.issn0736-8046
dc.identifier.issn1525-1470
dc.identifier.issue1en_US
dc.identifier.pmid23869531en_US
dc.identifier.scopus2-s2.0-84891859675en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage99en_US
dc.identifier.urihttps://doi.org/10.1111/pde.12163
dc.identifier.urihttps://hdl.handle.net/11616/96316
dc.identifier.volume31en_US
dc.identifier.wosWOS:000330951800033en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.relation.ispartofPediatric Dermatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject[No Keywords]en_US
dc.titleVogt-Koyanagi-Harada Disease in an Adolescent Boyen_US
dc.typeArticleen_US

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