(Q35863951)

10 August 2017

1 reference

title

From slow virus to prion: a review of transmissible spongiform encephalopathies (English)

1 reference

10 August 2017

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Lantos PL

1

1 reference

10 August 2017

publication date

1 January 1992

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10 August 2017

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10 August 2017

volume

20

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10 August 2017

issue

1

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10 August 2017

page(s)

1-11

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Experimental transmission of a Kuru-like syndrome to chimpanzees

10 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Experimental "kuru" in chimpanzees. A pathological report

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Familial Creutzfeldt-Jakob disease in Japan. Three cases in a family with white matter involvement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Syndromes of amyotrophic lateral sclerosis and dementia: relation to transmissible Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Reevaluation of the ultrastructural pathology of experimental Creutzfeldt-Jakob disease. Serial studies of the Fujisaki strain of Creutzfeldt-Jakob disease virus in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Spongiform encephalopathy transmitted experimentally from Creutzfeldt-Jakob and familial Gerstmann-Sträussler-Scheinker diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Neuropathologic verification of Creutzfeldt-Jakob disease in the exhumed American recipient of human pituitary growth hormone: epidemiologic and pathogenetic implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Creutzfeldt-Jakob disease following pituitary-derived human growth hormone therapy: a new American case.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Inherited human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Encephalopathy in mice produced by inoculation with scrapie brain material.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Encephalopathy of mink. I. Epizootiologic and clinical observations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

A novel progressive spongiform encephalopathy in cattle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Bovine spongiform encephalopathy: detection and quantitation of fibrils, fibril protein (PrP) and vacuolation in brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Fibrils from brains of cows with new cattle disease contain scrapie-associated protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

CHRONIC WASTING DISEASE OF CAPTIVE MULE DEER: A SPONGIFORM ENCEPHALOPATHY

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Spongiform encephalopathy of Rocky Mountain elk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Novel proteinaceous infectious particles cause scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Scrapie agent contains a hydrophobic protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

21 January 2018

On the biology of prions

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Immunohistochemical localization of prion protein in spongiform encephalopathies and normal brain tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Scrapie-associated prion protein accumulates in astrocytes during scrapie infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Molecular biology of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

Prion dementia without characteristic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

A simple and effective method for inactivating virus infectivity in formalin‐fixed tissue samples from patients with Creutzfeldt‐Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2559.1992.TB00909.X

10.1111/J.1365-2559.1992.TB00909.X

21 January 2018

Identifiers

DOI

1 reference

10 August 2017

1 reference