Eosinophilia and related hematological disorders: Review

dc.contributor.authorAltintaş A.
dc.contributor.authorÖzmen Ş.
dc.contributor.authorAyyildiz O.
dc.date.accessioned2024-04-24T18:43:38Z
dc.date.available2024-04-24T18:43:38Z
dc.date.issued2007
dc.departmentDicle Üniversitesien_US
dc.description.abstractEosinophilia 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.endpage717en_US
dc.identifier.issn1300-0292
dc.identifier.issue5en_US
dc.identifier.scopus2-s2.0-37049037763en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage711en_US
dc.identifier.urihttps://hdl.handle.net/11468/24230
dc.identifier.volume27en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.publisherTurkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEosinophiliaen_US
dc.subjectHypereosinophilic Syndromeen_US
dc.titleEosinophilia and related hematological disorders: Reviewen_US
dc.title.alternativeEozinofili ve ilişkili hematolojik hastaliklaren_US
dc.typeReview Articleen_US

Dosyalar