Eosinophilia and related hematological disorders: Review
dc.contributor.author | Altintaş A. | |
dc.contributor.author | Özmen Ş. | |
dc.contributor.author | Ayyildiz O. | |
dc.date.accessioned | 2024-04-24T18:43:38Z | |
dc.date.available | 2024-04-24T18:43:38Z | |
dc.date.issued | 2007 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Eosinophilia is defined by an eosinophile count of >600/mm3; it may be primary or secondary due to the underlying cause. End-organ damage may develop in familial form as well as primary or secondary eosinophilia and it may also develop regardless of a specific cause in severe or mild eosinophilia;. Recently, the pathogenesis of clonal hypereosinophilia is well recognized and different variants are defined. Copyright © 2007 by Türkiye Klinikleri. | en_US |
dc.identifier.endpage | 717 | en_US |
dc.identifier.issn | 1300-0292 | |
dc.identifier.issue | 5 | en_US |
dc.identifier.scopus | 2-s2.0-37049037763 | en_US |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.startpage | 711 | en_US |
dc.identifier.uri | https://hdl.handle.net/11468/24230 | |
dc.identifier.volume | 27 | en_US |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | tr | en_US |
dc.publisher | Turkiye Klinikleri | en_US |
dc.relation.ispartof | Turkiye Klinikleri Journal of Medical Sciences | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Eosinophilia | en_US |
dc.subject | Hypereosinophilic Syndrome | en_US |
dc.title | Eosinophilia and related hematological disorders: Review | en_US |
dc.title.alternative | Eozinofili ve ilişkili hematolojik hastaliklar | en_US |
dc.type | Review Article | en_US |