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dc.contributor.authorOftedal, Linn Silje Wathne
dc.contributor.authorMaple-Gørdem, Jodi
dc.contributor.authorTysnes, Ole-Bjørn
dc.contributor.authorAlves, Guido Werner
dc.contributor.authorLange, Johannes
dc.date.accessioned2023-10-18T09:30:32Z
dc.date.available2023-10-18T09:30:32Z
dc.date.created2023-09-26T12:45:35Z
dc.date.issued2023
dc.identifier.issn1877-7171
dc.identifier.urihttps://hdl.handle.net/11250/3097225
dc.description.abstractSeed amplification assays (SAA) are the first credible molecular assay for Parkinson’s disease (PD). However, the value of SAA to support the clinicians’ initial diagnosis of PD is not clear. In our study, we analyzed cerebrospinal fluid samples from 121 PD patients recruited through population screening methods and taken within a median delay of 38 days from diagnosis and 51 normal controls without neurodegenerative disease. SAA yielded a sensitivity of 82.6% (95% CI, 74.7% – 88.9%) and specificity of 88.2% (95% CI, 76.1% – 95.6%). These results highlight the potential of SAA to support the initial diagnosis of PD in clinical practice and research.en_US
dc.language.isoengen_US
dc.publisherIOS Pressen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleSeed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson's Diseaseen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 the authorsen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.3233/JPD-230065
dc.identifier.cristin2179010
dc.source.journalJournal of Parkinson's Diseaseen_US
dc.source.pagenumber841-844en_US
dc.identifier.citationJournal of Parkinson's Disease. 2023, 13 (5), 841-844.en_US
dc.source.volume13en_US
dc.source.issue5en_US


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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