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Volume 12, Number 12—December 2006
Perspective

On the Question of Sporadic or Atypical Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob Disease

Paul Brown*Comments to Author , Lisa M. McShane†, Gianluigi Zanusso‡, and Linda Detwiler§
Author affiliations: *Bethesda, Maryland, USA; †National Institutes of Health, Bethesda, Maryland, USA; ‡University of Verona, Verona, Italy,; §Virginia-Maryland Regional College of Veterinary Medicine, College Park, Maryland, USA

Main Article

Figure 1

Distribution of ages at onset of illness in 500 cases of neuropathologically verified or experimentally transmitted sporadic Creutzfeldt-Jakob disease. Approximately 10% of cases occur in patients during the middle third (25–49 years) of a human lifespan, which corresponds to age in cattle of ≈7–13 years.

Figure 1. Distribution of ages at onset of illness in 500 cases of neuropathologically verified or experimentally transmitted sporadic Creutzfeldt-Jakob disease. Approximately 10% of cases occur in patients during the middle third (25–49 years) of a human lifespan, which corresponds to age in cattle of ≈7–13 years.

Main Article

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Page updated: October 04, 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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