Eosinophilia and related hematological disorders

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dc.contributor.authorAltintas, Abdullah
dc.contributor.authorOezmen, Sehmus
dc.contributor.authorAyyildiz, Orhan
dc.date.accessioned2024-04-24T17:40:14Z
dc.date.available2024-04-24T17:40:14Z
dc.date.issued2007
dc.departmentDicle Üniversitesien_US
dc.description.abstractEosinophilia is defined by an eosinophile count of >600/mm(3); 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.en_US
dc.identifier.endpage717en_US
dc.identifier.issn1300-0292
dc.identifier.issn2146-9040
dc.identifier.issue5en_US
dc.identifier.startpage711en_US
dc.identifier.urihttps://hdl.handle.net/11468/21698
dc.identifier.volume27en_US
dc.identifier.wosWOS:000254582800012
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isotren_US
dc.publisherOrtadogu Ad Pres & Publ Coen_US
dc.relation.ispartofTurkiye Klinikleri Tip Bilimleri Dergisi
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 disordersen_US
dc.titleEosinophilia and related hematological disorders
dc.typeReview Articleen_US

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