Correlations between the clustering patterns of the pathological changes in sporadic Creutzfeldt-Jakob disease

Neuroscience Research Communications

Volumn 29, Issue 2, 2001, Pages 89-98

  Armstrong, R A ^a   Lantos, P L ^b   Cairns, N J ^b  

^a ASTON UNIVERSITY   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

Cerebellum; Cerebral cortex; Creutzfeldt Jakob disease; Prion protein deposition; Spatial pattern; Surviving neurons; Vacuolation

Indexed keywords

PRION PROTEIN;

ADULT; AGED; ARTICLE; BRAIN CORTEX; BRAIN REGION; CELL SURVIVAL; CELL VACUOLE; CEREBELLUM; CLINICAL ARTICLE; CORRELATION FUNCTION; CREUTZFELDT JAKOB DISEASE; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MALE; MORPHOMETRICS; NERVE CELL; NEUROPATHOLOGY; TISSUE DISTRIBUTION;

EID: 0034758788     PISSN: 08936609     EISSN: None     Source Type: Journal    
DOI: 10.1002/nrc.1030     Document Type: Article

References (29)

1. Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries 1993-1995
2. A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. 1. Clinical features
3. Is ataxic gait the predominant presenting manifestation of Creutzfeldt-Jakob disease? Experience of 14 Chinese cases from Taiwan
4. Clinical characteristics of familial and sporadic Creutzfeldt-Jakob disease in Finland
5. Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease): The nature and progression of spongiform change
6. Neuropathology of Creutzfeldt-Jakob disease in Japan: With special reference to the panencephalopathic type
7. Immunohistochemical study of microglia in the Creutzfeldt-Jakob diseased brain
8. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease
9. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (Prion diseases)
10. Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease
11. Cerebral amyloid in human prion disease
12. Microglia and the development of spongiform change in Creutzfeldt-Jakob disease
13. Reactive microglia in Creutzfeldt-Jakob disease
14. Characterization of the microglial response in murine scrapie
15. The spatial pattern of the vacuolation in patients with sporadic Creutzfeldt-Jakob disease
16. The spatial patterns of prion protein deposits in Creutzfeldt-Jakob disease: Comparison with βamyloid deposits in Alzheimer's disease
17. Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease
18. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
19. Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
20. Generation of monoclonal antibodies against human prion proteins in PrPO/O mice
21. Prion protein immunocytochemistry helps to establish the true incidence of prion diseases
22. Immunohistochemical study of kuru plaques using antibodies against synthetic prion protein peptides
23. Correlations between the morphology of diffuse and primitive β-amyloid (Aβ) deposits and the frequency of associated cells in Down's syndrome
24. The usefulness of spatial pattern analysis in understanding the pathogenesis of neurodegenerative disorders, with special reference to plaque formation in Alzheimer's disease
25. Analysis of spatial patterns in histological sections of brain tissue
26. Clustering of ipsilateral cortico-cortical projection neurons to area 7 in the rhesus monkey
27. Is the clustering of neurofibrillary tangles in Alzheimer's patients related to the cells of origin of specific corticocortical projections?
28. The role of cortical connectivity in Alzheimer's disease pathogenesis: A review and model system