The fitting of general force-of-infection models to wildlife disease prevalence data.
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Interacting Effects of Newcastle Disease Transmission and Illegal Trade on a Wild Population of White-Winged Parakeets in Peru: A Modeling ApproachUpper respiratory tract disease, force of infection, and effects on survival of gopher tortoisesReconstruction of Rift Valley fever transmission dynamics in Madagascar: estimation of force of infection from seroprevalence surveys using Bayesian modellingInferring infection hazard in wildlife populations by linking data across individual and population scales.Identifying the age cohort responsible for transmission in a natural outbreak of Bordetella bronchisepticaEstimating Loss of Brucella Abortus Antibodies from Age-Specific Serological Data In Elk.The impact of disease on the survival and population growth rate of the Tasmanian devil.Integrated survival analysis using an event-time approach in a Bayesian frameworkIntensive Circulation of Japanese Encephalitis Virus in Peri-urban Sentinel Pigs near Phnom Penh, Cambodia.Deciphering serology to understand the ecology of infectious diseases in wildlife.Elucidating transmission dynamics and host-parasite-vector relationships for rodent-borne Bartonella spp. in Madagascar.Chronic wasting disease in white-tailed deer: infection, mortality, and implications for heterogeneous transmission.Emerging prion disease drives host selection in a wildlife population.Probable causes of increasing brucellosis in free-ranging elk of the Greater Yellowstone Ecosystem.Spatial and temporal patterns of chronic wasting disease: fine-scale mapping of a wildlife epidemic in Wisconsin.Revisiting Rayong: shifting seroprofiles of dengue in Thailand and their implications for transmission and control.Pathogen exposure varies widely among sympatric populations of wild and domestic felids across the United States.Mycobacteriosis-associated mortality in wild striped bass (Morone saxatilis) from Chesapeake Bay, U.S.A.Evidence of multiple intraspecific transmission routes for Leptospira acquisition in Norway rats (Rattus norvegicus).Chronic wasting disease in a Wisconsin white-tailed deer farm.Adjusting age and stage distributions for misclassification errors.The epidemiology underlying age-related avian malaria infection in a long-lived host: the mute swanCygnus olorUnderestimating the effects of spatial heterogeneity due to individual movement and spatial scale: infectious disease as an exampleAvian malaria in Hawaiian forest birds: infection and population impacts across species and elevations
P2860
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P2860
The fitting of general force-of-infection models to wildlife disease prevalence data.
description
2006 nî lūn-bûn
@nan
2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
The fitting of general force-of-infection models to wildlife disease prevalence data.
@ast
The fitting of general force-of-infection models to wildlife disease prevalence data.
@en
type
label
The fitting of general force-of-infection models to wildlife disease prevalence data.
@ast
The fitting of general force-of-infection models to wildlife disease prevalence data.
@en
prefLabel
The fitting of general force-of-infection models to wildlife disease prevalence data.
@ast
The fitting of general force-of-infection models to wildlife disease prevalence data.
@en
P2093
P2860
P1433
P1476
The fitting of general force-of-infection models to wildlife disease prevalence data.
@en
P2093
Damien O Joly
Dennis M Heisey
François Messier
P2860
P304
P356
10.1890/0012-9658(2006)87[2356:TFOGFM]2.0.CO;2
P407
P577
2006-09-01T00:00:00Z