E
Eystein Skjerve
Researcher at Norwegian University of Life Sciences
Publications - 232
Citations - 8651
Eystein Skjerve is an academic researcher from Norwegian University of Life Sciences. The author has contributed to research in topics: Population & Seroprevalence. The author has an hindex of 48, co-authored 224 publications receiving 7655 citations. Previous affiliations of Eystein Skjerve include Centers for Disease Control and Prevention & Hawassa University.
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Magnetic separation techniques in diagnostic microbiology.
TL;DR: IMS has been demonstrated to be a useful method in diagnostic microbiology and described as a method for enhancing the specificity and sensitivity of other detection systems, such as PCR, and providing considerable savings in time compared with traditional diagnostic systems.
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Risk factors for sporadic Campylobacter infections: results of a case-control study in southeastern Norway.
TL;DR: In 1989 and 1990, a case-control study designed to identify risk factors for sporadic infections with thermotolerant Campylobacter bacteria was conducted in three counties in southeastern Norway, finding the risk associated with consumption of sausages at a barbecue could not be attributed to cross-contamination from poultry products.
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Epidemiological investigation of risk factors for Campylobacter colonization in Norwegian broiler flocks
Georg Kapperud,Eystein Skjerve,L. Vik,K. Hauge,A. Lysaker,I. Aalmen,S. M. Ostroff,M. E. Potter +7 more
TL;DR: The results indicate that disinfection of drinking water is the preventive measure most likely to have the greatest impact on the prevalence of campylobacter among broiler chicken flocks in the study area.
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Detection of Listeria monocytogenes in foods by immunomagnetic separation.
TL;DR: The Immunomagnetic separation with immunomagnetic beads method represents a new approach to extraction and isolation of pathogenic bacteria directly from foods, after resuscitation, or from enrichment broths.
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Detection of pathogenic Yersinia enterocolitica in foods and water by immunomagnetic separation, nested polymerase chain reactions, and colorimetric detection of amplified DNA
TL;DR: The PCR assay identified all common pathogenic serogroups from three continents and differentiated pathogenic Y. enterocolitica from Y. pseudotuberculosis and from a variety of nonpathogenic yersiniae representing 25 serog groups and four species.