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Volume 11, Number 9—September 2005
Research

Variant Creutzfeldt-Jakob Disease Death, United States

Ermias D. Belay*Comments to Author , James J. Sejvar*, Wun-Ju Shieh*, Steven T. Wiersma†, Wen-Quan Zou‡, Pierluigi Gambetti‡, Stephen Hunter*, Ryan A. Maddox*, Landis Crockett†, Sherif R. Zaki*, and Lawrence B. Schonberger*
Author affiliations: *Centers for Disease Control and Prevention, Atlanta, Georgia, USA; †Florida Department of Health, Tallahassee, Florida, USA; ‡Case Western Reserve University, Cleveland, Ohio, USA

Main Article

Figure 2

Immunohistochemical staining of cerebellar tissue of the patient who died of variant Creutzfeldt-Jakob disease in the United States. Stained amyloid plaques are shown with surrounding deposits of abnormal prion protein (immunoalkaline phosphatase stain, naphthol fast red substrate with light hematoxylin counterstain; original magnification ×158).

Figure 2. . Immunohistochemical staining of cerebellar tissue of the patient who died of variant Creutzfeldt-Jakob disease in the United States. Stained amyloid plaques are shown with surrounding deposits of abnormal prion protein (immunoalkaline phosphatase stain, naphthol fast red substrate with light hematoxylin counterstain; original magnification ×158).

Main Article

Page created: April 23, 2012
Page updated: April 23, 2012
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