Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/39278
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dc.contributor.authorTekelioglu, UY-
dc.contributor.authorSerin, S-
dc.contributor.authorKiter, G-
dc.contributor.authorSungurtekin, H-
dc.date.accessioned2022-02-28T07:13:53Z
dc.date.available2022-02-28T07:13:53Z
dc.date.issued2013-
dc.identifier.issn2149-5807-
dc.identifier.urihttps://hdl.handle.net/11499/39278-
dc.identifier.urihttps://doi.org/10.5152/jaem.2011.059-
dc.description.abstractIdiopathic hypereosinophilic syndrome (HES) is a rare disorder of unknown etiology characterized by eosinophilia of at least six-months duration and organ involvement due to eosinophilia. Moreover, at the beginning of the case of HES, presenting with ARDS is rarely seen. We present our case according to those uncommon features.en_US
dc.language.isotren_US
dc.publisherAVESen_US
dc.relation.ispartofEURASIAN JOURNAL OF EMERGENCY MEDICINEen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHypereosinophilic syndrome; ARDS; pulmonary involvementen_US
dc.titleHypereosinophilic Syndrome with Pulmonary Involvement As a Rare Cause ofen_US
dc.typeArticleen_US
dc.identifier.volume12en_US
dc.identifier.issue2en_US
dc.identifier.startpage105
dc.identifier.startpage105en_US
dc.identifier.endpage108en_US
dc.identifier.doi10.5152/jaem.2011.059-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.wosWOS:000420175800013en_US
dc.ownerPamukkale University-
item.grantfulltextnone-
item.openairetypeArticle-
item.languageiso639-1tr-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.dept14.01. Surgical Medicine-
Appears in Collections:Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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