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An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques.

Subjects: *CREUTZFELDT-Jakob disease diagnosis; *CEREBELLUM; *CEREBRAL cortex

  • Source: Neuropathology. Jun2017, Vol. 37 Issue 3, p241-248. 8p.

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Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.

Subjects: PRION diseases; NEURONS; CREUTZFELDT-Jakob disease

  • Source: Neuropathology & Applied Neurobiology. Aug2011, Vol. 37 Issue 5, p500-512. 13p. 1 Color Photograph, 2 Charts, 4 Graphs.

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A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt–Jakob disease (vCJD).

Subjects: CEREBELLUM; PLAQUES & plaquettes; PURKINJE cells

  • Source: Neuropathology & Applied Neurobiology. Feb2009, Vol. 35 Issue 1, p36-45. 10p. 1 Black and White Photograph, 1 Diagram, 5 Charts, 1 Graph.

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Academic Journal

Extensive cortical spongiform changes with cerebellar small amyloid plaques: The clinicopathological case of MV2K+ C subtype in Creutzfeldt- Jakob disease.

Subjects: *CREUTZFELDT-Jakob disease; *CENTRAL nervous system diseases; *AMYLOID plaque

  • Source: Neuropathology. Dec2014, Vol. 34 Issue 6, p541-546. 6p.

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An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology.

Subjects: *CREUTZFELDT-Jakob disease; *DEMENTIA; *PNEUMONIA

  • Source: Neuropathology. Apr2010, Vol. 30 Issue 2, p159-164. 6p. 1 Color Photograph, 1 Chart.

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Academic Journal

Autopsy case of Creutzfeldt–Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum.

Subjects: *CREUTZFELDT-Jakob disease; *KURU; *PROTEOLYTIC enzymes

  • Source: Neuropathology. Aug2006, Vol. 26 Issue 4, p313-317. 5p. 3 Diagrams.

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Academic Journal

Quantification of vacuolation (‘spongiform change’), surviving neurones and prion protein deposition in eleven cases of variant Creutzfeldt–Jakob disease.

Subjects: *CREUTZFELDT-Jakob disease; *PRIONS

  • Source: Neuropathology & Applied Neurobiology. Apr2002, Vol. 28 Issue 2, p129-135. 7p.

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Academic Journal

Apoptotic bodies in the cerebellum of Japanese patients with Creutzfeldt–Jakob disease.

Subjects: *CREUTZFELDT-Jakob disease; *APOPTOSIS; *CEREBELLUMJAPAN

  • Source: Pathology International. Mar2001, Vol. 51 Issue 3, p140-144. 5p. 4 Black and White Photographs, 1 Chart.

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Academic Journal

Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt–Jakob disease.

Subjects: *CREUTZFELDT-Jakob disease; *CENTRAL nervous system diseases; *PRION diseases

  • Source: Neuropathology. Mar2001, Vol. 21 Issue 1, p19-24. 6p. 2 Black and White Photographs, 2 Charts, 2 Graphs.

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Academic Journal

Cerebellar basket cells of Creutzfeldt–Jakob disease: Immunohistochemical and ultrastructural study.

Subjects: *CREUTZFELDT-Jakob disease; *CEREBELLUM; *NEUROLOGICAL disorders

  • Source: Pathology International. Apr2000, Vol. 50 Issue 4, p291-296. 6p.

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  • 1-10 of  30 results for ""CREUTZFELDT-Jakob disease""