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Correspondence
August 2009

Identification of Creutzfeldt-Jakob Disease Variants—Reply

Arch Neurol. 2009;66(8):1045-1046. doi:10.1001/archneurol.2009.144

In reply

We thank Dr Barash for his comments regarding the data presented in our article.1 While we are in strong agreement with Dr Barash, we want to ensure that readers are aware that the affective cases in our study are not cases of vCJD. Nine of the 13 cases (69.2%) underwent postmortem examination and did not have neuropathological or prion protein strain characteristics typical of vCJD.2 Thus, all neuropathologically confirmed cases in our article were of the sCJD type.

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