Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5482
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dc.contributor.authorAraj, George F.en_US
dc.contributor.authorBeaini, Monaen_US
dc.contributor.authorBizri, Nazih A.en_US
dc.contributor.authorGhizzawi, Layanen_US
dc.date.accessioned2022-04-12T06:52:59Z-
dc.date.available2022-04-12T06:52:59Z-
dc.date.issued2020-
dc.identifier.issn00239852-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5482-
dc.description.abstractThe laboratory diagnosis of COVID-19 is essentially based on three modalities. The reference method in lieu of viral culture is the molecular amplification assays, mostly by using the real-time reverse-transcriptase polymerase chain reaction (RT-PCR). However, due to its complexity, needed equipment and expertise as well as the high expense, other assay modalities have been introduced. These include antigen-based and antibody-based detection assays. This article provides a consolidated approach that will shed light on the different formats and utilities that these assays are intended for at this stage in time, addressing when, who, and what in the testing of COVID-19. It is worth noting that a combination of different assays is advisable to settle interpretation of test results to reflect the true scope of the patient’s condition.en_US
dc.language.isoengen_US
dc.subjectCOVID-19en_US
dc.subjectLab diagnosisen_US
dc.subjectRapid testingen_US
dc.titleTesting for COVID-19: When, who, and what test?en_US
dc.typeJournal Articleen_US
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume68en_US
dc.description.issue1-2en_US
dc.description.startpage16en_US
dc.description.endpage26en_US
dc.date.catalogued2022-04-12-
dc.description.statusPublisheden_US
dc.identifier.openURLhttps://lebanesemedicaljournal.org/Home/ArticleDetails/30786en_US
dc.relation.ispartoftextJournal Medical Libanaisen_US
dc.description.campusSGH campusen_US
Appears in Collections:Faculty of Medicine
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