Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/24114
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dc.contributor.authorSarbay, Hakan-
dc.contributor.authorSarbay, BC-
dc.contributor.authorAkjn, M-
dc.contributor.authorKocamaz, Halil-
dc.contributor.authorTosun, MS-
dc.date.accessioned2019-08-20T06:59:57Z
dc.date.available2019-08-20T06:59:57Z
dc.date.issued2017-
dc.identifier.issn2090-6560-
dc.identifier.urihttps://hdl.handle.net/11499/24114-
dc.identifier.urihttps://doi.org/10.1155/2017/6341321-
dc.description.abstractCeliac disease (CD) is an immunological disorder. Clinical manifestations occur as a result of intestinal mucosa damage and malabsorption. CD is also associated with extraintestinal manifestations and autoimmune disorders. The coexistence of CD and autoimmune diseases has been described before. In this article, a patient with CD presenting with thrombocytopenia is discussed.en_US
dc.language.isoenen_US
dc.publisherHINDAWI LTDen_US
dc.relation.ispartofCASE REPORTS IN HEMATOLOGYen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleCeliac Disease Presenting with Immune Thrombocytopenic Purpuraen_US
dc.typeReporten_US
dc.identifier.startpage1
dc.identifier.startpage1en_US
dc.identifier.endpage3en_US
dc.authorid0000-0002-3366-1695-
dc.identifier.doi10.1155/2017/6341321-
dc.relation.publicationcategoryDiğeren_US
dc.identifier.pmid28424750en_US
dc.identifier.wosWOS:000397777600001en_US
dc.ownerPamukkale University-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairetypeReport-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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