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Published byOswin Stephens Modified over 5 years ago
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Quantitative variations in the pathology of 11 cases of variant Creutzfeldt–Jakob disease (vCJD)
R.A Armstrong, N.J Cairns, J.W Ironside, P.L Lantos Pathophysiology Volume 8, Issue 4, Pages (August 2002) DOI: /S (02)
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Fig. 1 PrP deposits in the frontal cortex of a case of vCJD. (A) Florid deposits consisting of darkly stained condensed cores and the more diffuse, lightly stained non-florid deposits; (B) large cluster of florid deposits associated with a cluster of vacuoles. (Section immunostained with 12F10 antibody). Pathophysiology 2002 8, DOI: ( /S (02) )
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Fig. 2 A plot of the 11 variant Creutzfeldt–Jakob cases (A–K) in relation to PC 1 and 2. Pathophysiology 2002 8, DOI: ( /S (02) )
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