Sensitive Commercial NASBA Assay for the Detection of Respiratory Syncytial Virus in Clinical Specimen

The aim of the study was to evaluate the usability of three diagnostic procedures for the detection of respiratory syncytial virus in clinical samples. Therefore, the FDA cleared CE marked NOW® RSV ELISA, the NucliSENS® EasyQ RSV A+B NASBA, and a literature based inhouse RT-PCR protocol were compare...

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Detalles Bibliográficos
Autores principales: Tillmann, Ramona Liza, Simon, Arne, Müller, Andreas, Schildgen, Oliver
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137935/
https://www.ncbi.nlm.nih.gov/pubmed/18159240
http://dx.doi.org/10.1371/journal.pone.0001357

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137935/
https://www.ncbi.nlm.nih.gov/pubmed/18159240
http://dx.doi.org/10.1371/journal.pone.0001357

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