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Eva R. Kallio

Researcher at University of Jyväskylä

Publications -  38
Citations -  1615

Eva R. Kallio is an academic researcher from University of Jyväskylä. The author has contributed to research in topics: Puumala virus & Bank vole. The author has an hindex of 20, co-authored 38 publications receiving 1445 citations. Previous affiliations of Eva R. Kallio include Finnish Forest Research Institute & University of Helsinki.

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Prolonged survival of Puumala hantavirus outside the host: evidence for indirect transmission via the environment

TL;DR: It is demonstrated that hantavirus transmission does not require direct contact between rodents, or between rodents and humans, and that the indirect transmission of PUUV through contaminated environment takes place among the rodents for a prolonged period of time.
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Host–pathogen time series data in wildlife support a transmission function between density and frequency dependence

TL;DR: This study illustrates how time series data of the host–pathogen dynamics, especially of the number of susceptible individuals, can greatly facilitate the fitting of mechanistic disease models.
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Endemic hantavirus infection impairs the winter survival of its rodent host.

TL;DR: This work examines the effect of Puumala virus (PUUV) infection on the winter survival of bank voles (Myodes glareolus), the host of this virus, to provide the first evidence for a significant effect of PUUV on host survival.
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Cyclic hantavirus epidemics in humans--predicted by rodent host dynamics.

TL;DR: The results suggest that although human hantavirus epidemics are preceded by high sero prevalence in the host population, they may be accurately predicted solely by the population dynamics of the carrier species, even without any knowledge about hantvirus dynamics in theHost populations.
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Cowpox with severe generalized eruption, Finland.

TL;DR: Cowpox with a severe, generalized eruption was diagnosed in an atopic 4-year-old girl by electron microscopy, virus isolation, polymerase chain reaction, and immunoglobulin (Ig) M and low-avidity IgG antibodies.