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Volume 12, Number 10—October 2006
Research

Human Prion Disease and Relative Risk Associated with Chronic Wasting Disease

W. John Pape†, Jeri Forster*, C. Alan Anderson‡§, Patrick Bosque‡¶, Patrick Bosque‡¶, Michael Miller#, and Samantha MaWhinney
Author affiliations: *University of Colorado at Denver and Health Sciences Center, Denver, Colorado, USA; †Colorado Department of Public Health and Environment, Denver, Colorado, USA; ‡University of Colorado School of Medicine, Denver, Colorado, USA; §Denver Veteran's Affairs Medical Center, Denver, Colorado, USA; ¶Denver Health Medical Center, Denver, Colorado, USA; #Colorado Division of Wildlife, Fort Collins, Colorado, USA

Main Article

Figure 1

Location of chronic wasting disease (CWD)–endemic area in northeastern Colorado, USA (7) (gray shading) in relationship to Colorado counties regarded as CWD counties (bold outline) for purposes of comparing Creutzfeldt-Jakob disease rates and relative risk among resident human populations.

Figure 1. Location of chronic wasting disease (CWD)–endemic area in northeastern Colorado, USA (7) (gray shading) in relationship to Colorado counties regarded as CWD counties (bold outline) for purposes of comparing Creutzfeldt-Jakob disease rates and relative risk among resident human populations.

Main Article

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Page updated: December 05, 2011
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The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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