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As cerebrospinal fluid biomarkers are gaining importance in clinical research and diagnostics of Alzheimer’s disease, there is a need for automated assays that are reliable, afford high throughput, and correlate with other assays. We evaluated the performance of the automated immunoassay system, LUMIPULSE G (FujiRebio), in relation to other immunoassays for measurement of the core Alzheimer’s disease biomarkers, determined intra- and inter-laboratory and longitudinal variability, and established clinical cut-points.

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This page is a summary of: Validation of the LUMIPULSE automated immunoassay for the measurement of core AD biomarkers in cerebrospinal fluid, Clinical Chemistry and Laboratory Medicine (CCLM), November 2021, De Gruyter,
DOI: 10.1515/cclm-2021-0651.
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