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dc.contributor.authorSenturk, N
dc.contributor.authorSahin, S
dc.contributor.authorKocagoz, T
dc.date.accessioned2020-06-21T15:45:12Z
dc.date.available2020-06-21T15:45:12Z
dc.date.issued2002
dc.identifier.issn0011-9059
dc.identifier.urihttps://doi.org/10.1046/j.1365-4362.2002.01604.x
dc.identifier.urihttps://hdl.handle.net/20.500.12712/21946
dc.descriptionWOS: 000179922100007en_US
dc.descriptionPubMed: 12492970en_US
dc.description.abstractBackground Most cutaneous tuberculosis lesions contain few bacilli, so identification of Mycobacterium tuberculosis in conventional laboratory tests is difficult. In vitro amplification of specific DNA sequences using polymerase chain reaction (PCR) has become a valuable tool in the rapid detection of slow-growing organisms like M. tuberculosis . Aim To investigate the presence of M. tuberculosis DNA in cutaneous tuberculosis. Methods Twenty-two archival biopsy specimens diagnosed as cutaneous tuberculosis were investigated for the presence of M. tuberculosis DNA by PCR. Normal skin samples of 29 healthy patients were used as a control. Results Amplification of the M. tuberculosis DNA was observed in one of the cutaneous tuberculosis specimens and in a healthy control. Conclusion Although PCR is a rapid diagnostic method, fixation procedures may decrease its sensitivity.en_US
dc.language.isoengen_US
dc.publisherBlackwell Publishing Ltden_US
dc.relation.isversionof10.1046/j.1365-4362.2002.01604.xen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titlePolymerase chain reaction in cutaneous tuberculosis: is it a reliable diagnostic method in paraffin-embedded tissues?en_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume41en_US
dc.identifier.issue12en_US
dc.identifier.startpage863en_US
dc.identifier.endpage866en_US
dc.relation.journalInternational Journal of Dermatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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