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dc.contributor.authorAcar, K.
dc.contributor.authorSucak, A.
dc.contributor.authorBeyazit, Y.
dc.contributor.authorGenc, G.
dc.contributor.authorHaznedaroglu, I. C.
dc.contributor.authorAksu, S.
dc.contributor.authorDanisman, N.
dc.date.accessioned2019-12-10T11:14:34Z
dc.date.available2019-12-10T11:14:34Z
dc.date.issued2007
dc.identifier.issn0300-0605
dc.identifier.urihttps://doi.org/10.1177/147323000703500516
dc.identifier.urihttp://hdl.handle.net/11655/15157
dc.description.abstractPre-eclampsia (PE) is a human pregnancy-specific disorder of unknown aetiology. Although the quantitative relationship between platelet aggregation in PE is not clearly defined yet, we aimed to investigate the possible relationship between PE and platelet glycoprotein V (GPV), which is an integral platelet membrane protein involved in the function of the GPIb-V-IX receptor. Fifty patients with PE and 37 normotensive pregnant women (controls) were enrolled in this study. Fasting blood samples were collected and soluble GPV (sGPV) levels were determined using a commercially available enzyme immunoassay. No statistically significant difference in sGPV was found between PE patients and control subjects. There was no correlation between sGPV and platelet counts or between pregnancy duration and platelet counts. Further clinical and experimental investigations are needed to elucidate the pathological processes involved in the development of PE in complicated pregnancies.
dc.language.isoen
dc.publisherSage Publications Inc
dc.relation.isversionof10.1177/147323000703500516
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectResearch & Experimental Medicine
dc.subjectPharmacology & Pharmacy
dc.titleLack of Platelet Activation Reflected by Circulating Soluble Glycoprotein V in Pre-Eclampsia
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalJournal Of International Medical Research
dc.contributor.departmentİç hastalıkları
dc.identifier.volume35
dc.identifier.issue5
dc.identifier.startpage704
dc.identifier.endpage708
dc.description.indexWoS
dc.description.indexScopus


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