The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system (Q40537007)

21 September 2017

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title

The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system (English)

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Creutzfeldt-Jakob disease

21 September 2017

1 reference

Richardson EP Jr

1

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PubMed ID

7767489

21 September 2017

Masters CL

series ordinal

2

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21 September 2017

1 January 1995

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21 September 2017

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21 September 2017

5

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21 September 2017

1

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21 September 2017

33-41

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Experimental transmission of a Kuru-like syndrome to chimpanzees

21 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Identification of a protein that purifies with the scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Scrapie prions aggregate to form amyloid-like birefringent rods

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.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.1750-3639.1995.TB00575.X

Subacute spongiform encephalopathy--a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.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.1750-3639.1995.TB00575.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.1750-3639.1995.TB00575.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.TB00575.X

Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Creutzfeldt-Jakob disease presenting as Wernicke-Korsakoff syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.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.TB00575.X

Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.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.1750-3639.1995.TB00575.X

The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Insertions in the prion protein gene in atypical dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Posterior cortical atrophy. Neuropathologic correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Different susceptibilities of the geniculate and extrageniculate visual pathways to human Creutzfeldt-Jakob disease (a combined neurophysiological-neuropathological study).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Analysis of the prion protein gene in thalamic dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.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.TB00575.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.1750-3639.1995.TB00575.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.TB00575.X

Gerstmann-Sträussler syndrome--a variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.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.TB00575.X

Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Geotropic ocular deviation with skew and absence of saccade in Creutzfelt-Jackob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Abnormal eye movements in Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Creutzfeldt-Jakob disease with severe involvement of cerebral white matter and cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Spongiform encephalopathy with extensive involvement of white matter.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Concomitant Creutzfeldt-Jakob and Alzheimer diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Demyelinating peripheral neuropathy in Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). Atypical clinical and pathological findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

The neurochemistry of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Evidence against the transmissibility of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Blood buffy coat from Alzheimer's disease patients and their relatives does not transmit spongiform encephalopathy to hamsters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Coexistence of Creutzfeldt-Jakob disease and Alzheimer's disease in the same patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

Prion protein is necessary for normal synaptic function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00575.X

10.1111/J.1750-3639.1995.TB00575.X

21 January 2018

Identifiers

DOI

1 reference

21 September 2017

1 reference

PubMed ID

7767489