(Q38476222)

3 September 2017

title

Pathology and immunocytochemistry of a kuru brain (English)

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3 September 2017

2

Liberski PP

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3 September 2017

Hainfellner JA

1

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3 September 2017

Guiroy DC

3

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3 September 2017

Cervénaková L

4

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3 September 2017

Brown P

5

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3 September 2017

Gajdusek DC

6

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3 September 2017

Budka H

7

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3 September 2017

publication date

1 January 1997

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3 September 2017

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3 September 2017

volume

7

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3 September 2017

issue

1

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3 September 2017

page(s)

547-553

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Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.

3 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Experimental kuru in the spider monkey. Histopathological and ultrastructural studies of the brain during early stages of incubation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Experimental kuru in the chimpanzee. A neuropathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Unconventional Viruses and the Origin and Disappearance of Kuru

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Relationship of microglia and scrapie amyloid-immunoreactive plaques in kuru, Creutzfeldt-Jakob disease and Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Localization of amyloidogenic proteins and sulfated glycosaminoglycans in nontransmissible and transmissible cerebral amyloidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Proteinase-resistant prion protein accumulation in Syrian hamster brain correlates with regional pathology and scrapie infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Further observations on the pathology of Kuru. (A study of the two cerebra in serial section).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Apolipoprotein E immunoreactivity in cerebral amyloid deposits and neurofibrillary tangles in Alzheimer's disease and kuru plaque amyloid in Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

Prion-protein immunoreactivity in human transmissible dementias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

A new variant of Creutzfeldt-Jakob disease in the UK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1997.TB01072.X

10.1111/J.1750-3639.1997.TB01072.X

21 January 2018

Identifiers

DOI

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3 September 2017

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