2016
DOI: 10.1016/j.jns.2016.04.049
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Nested polymerase chain reaction in cerebrospinal fluid for diagnosing spinal cord schistosomiasis: A promising method

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Cited by 24 publications
(7 citation statements)
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“…Moreover, these techniques seem to implicate high specificity (100%) and sensitivity (80%) compared with our standard laboratory tests. Only a few studies have evaluated this method, and future studies with a high quality of methodical designing are warranted [12]. …”
Section: Discussionmentioning
confidence: 99%
“…Moreover, these techniques seem to implicate high specificity (100%) and sensitivity (80%) compared with our standard laboratory tests. Only a few studies have evaluated this method, and future studies with a high quality of methodical designing are warranted [12]. …”
Section: Discussionmentioning
confidence: 99%
“…Nested PCR (nPCR) is a more sensitive and a specific approach than cPCR, and has been successfully applied in different instances in the diagnosis of schistosomiasis [ 46 , 76 ]. However, the procedure includes duplication of cPCR for the initial amplification of a larger gene fragment and then another sequence within the initial fragment, which involves more labor and a higher cost.…”
Section: Dna-based Diagnostics For Schistosomiasismentioning
confidence: 99%
“…Schistosome cfDNA detection is an ideal option to diagnose these cases either using serum or non-invasive clinical samples like urine [ 114 ]. Furthermore, cfDNA detection is helpful in situations such as neuroschistosomiasis, where parasite DNA can be detected in host cerebrospinal fluid [ 46 , 120 ].…”
Section: Applications Of Dna Diagnostics For Schistosomiasismentioning
confidence: 99%
“…The nested PCR (nPCR) involves two primers in two successive runs of the test, where the second amplifies a secondary target within the product of the first run. The advantage is that this limits non-specificity by only permitting a low number of first runs (Bruscky et al, 2016). Quantitative PCR (qPCR), also named real-time PCR, monitors the amplification of the targeted DNA in real time as opposed to only measuring the end product, which not only results in better specificity but also provides a value of the infection intensity (Guegan et al, 2019).…”
Section: Introductionmentioning
confidence: 99%