(Q34737100)

4 August 2017

title

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

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Creutzfeldt-Jakob disease

4 August 2017

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8

Hauw JJ

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4 August 2017

Budka H

1

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4 August 2017

Aguzzi A

2

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4 August 2017

Brown P

3

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4 August 2017

Brucher JM

4

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4 August 2017

Bugiani O

5

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4 August 2017

Gullotta F

6

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4 August 2017

Haltia M

7

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4 August 2017

Ironside JW

9

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4 August 2017

Jellinger K

10

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4 August 2017

publication date

1 October 1995

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4 August 2017

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4 August 2017

volume

5

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4 August 2017

issue

4

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4 August 2017

page(s)

459-466

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Miniplaques and shapeless cerebral amyloid deposits in a case of Gerstmann-Sträussler-Scheinker's syndrome

4 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Prion dementia without characteristic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Creutzfeldt-Jakob disease and cerebral amyloid angiopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Inherited human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Prion protein immunocytochemistry helps to establish the true incidence of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

Absence of protease-resistant prion protein in dementia characterized by neuronal loss and status spongiosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00625.X

10.1111/J.1750-3639.1995.TB00625.X

21 January 2018

Identifiers

DOI

1 reference

4 August 2017

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