Conclusion: PCR methods for the detection and identification of enteroviruses were useful for the diagnosis of enteroviral infection in CNS.
We describe a new approach for the detection and identification of actinides at low activity levels directly in aqueous solution.
Such information is essential for the use of the NV− centre for the detection and identification of radicals or relaxation centres, and for the transduction of chemically informative NMR spectra by optical means.
This paper presents a new method for the detection and identification of multiple linear and nonlinear scatterers by combining nonlinear elastic wave spectroscopy, time reversal and DORT method.
To compare polymerase chain reaction (PCR) to microbial culture for the detection and identification of bacterial and fungal pathogens in microbial keratitis.
DNA microarray technology has become a promising new tool for the detection and identification of viral pathogens in human plasma and cell cultures.
Development of a generally applicable sensitive hybridization-based assay devoid of any target amplification for the detection and identification of (pathogenic) bacterial and viral species.
This paper investigates the feasibility of a cost effective high gradient magnetic separation based device for the detection and identification of malaria parasites in a blood sample.
The samples were tested for the presence of enteroviruses by cell culture and PCR methods for the detection and identification of enteroviruses.
In conclusion, this newly developed mRT-PCR provides a rapid, sensitive and reliable method for the detection and identification of major garlic viruses.
In the present study a simple and reliable assay based on nested PCR was developed for the detection and identification of Leishmania parasites from rodent skin samples.
