Titlebook: Applied Virology Research; New Diagnostic Proce Edouard Kurstak,R. G. Marusyk,M. H. V. Regenmortel Book 1994 Springer Science+Business Medi

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Fast Multiplex Polymerase Chain Reaction on Boiled Clinical Samples for Rapid Diagnosis of Viral Inmoment. Final identification of virus isolates usually depends on serologic tests and sometimes on morphologic, biophysical, or biologic characterization. The polymerase chain reaction (PCR) has the potential to replace these laborious viral isolation methods, but problems such as specificity, repro

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Automation of the Detection of DNA Sequences for the Laboratory Diagnosis of Viral Infections,ent of viral disease. In particular, a more precise and timely diagnosis is rendered possible, with the resultant advantages in treatment. For the clinical laboratory, time and labor can be reduced, procedures simplified, and organisms which are fastidious to culture can be identified more readily (Tenover, 1988).

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https://doi.org/10.1007/978-3-031-09924-3nician. Currently, however, the role of viruses in infections tend to be increasingly recognized particularly in the immunocompromised patient, the neonate and in sexually transmitted diseases. Furthermore, the recent advances in chemotherapy of viral diseases particularly for serious herpesvirus in

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https://doi.org/10.1007/978-3-642-79820-7c. By July, 1993, more than 150 countries had reported over 718,894 cases to the World Health Organization (WHO, 1993), and more than 8 million persons worldwide were estimated to be infected with the human immunodeficiency virus type 1 (HIV-1), the etiologic agent of AIDS. There are estimated to be

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J. F. McGlip,D. Weaire,C. H. Pattersoncid hybridization made detection of target sequences highly specific and/or relatively rapid in comparison to standardized immunological or culture-based assays, the methodology was slow in being adapted to clinical settings for two major reasons. First, the most sensitive nucleic acid hybridization

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