Creutzfeldt-Jakob disease, new variant creutzfeldt-jakob disease, and bovine spongiform encephalopathy (Q33750275)

29 July 2017

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title

Creutzfeldt-Jakob disease, new variant creutzfeldt-jakob disease, and bovine spongiform encephalopathy (English)

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Creutzfeldt-Jakob disease

29 July 2017

main subject

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Weihl CC

1

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29 July 2017

Roos RP

series ordinal

2

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29 July 2017

publication date

1 November 1999

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29 July 2017

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29 July 2017

volume

17

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29 July 2017

issue

4

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29 July 2017

page(s)

835-859

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

29 July 2017

cites work

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7 January 2021

Non-genetic propagation of strain-specific properties of scrapie prion protein.

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7 January 2021

Identification of a protein that purifies with the scrapie prion

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7 January 2021

Can Creutzfeldt-Jakob disease be transmitted by transfusion?

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7 January 2021

The distribution of infectivity in blood components and plasma derivatives in experimental models of transmissible spongiform encephalopathy

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7 January 2021

AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE)

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7 January 2021

Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

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7 January 2021

Mice devoid of PrP are resistant to scrapie

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7 January 2021

Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease

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7 January 2021

Encephalopathy in mice produced by inoculation with scrapie brain material.

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7 January 2021

Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.

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7 January 2021

Presence of the transmissible agent of scrapie in the serum of affected mice and rats

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7 January 2021

Pathologic conformations of prion proteins

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7 January 2021

Hippocampal slices from prion protein null mice: disrupted Ca(2+)-activated K+ currents.

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7 January 2021

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

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7 January 2021

Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study

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7 January 2021

Predicting the CJD epidemic in humans

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7 January 2021

Diffusion-weighted MRI in sporadic Creutzfeldt-Jakob disease

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7 January 2021

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Letter: Hepatitis with hindsight

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7 January 2021

Experimental transmission of a Kuru-like syndrome to chimpanzees

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7 January 2021

Nature of the Scrapie Agent

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7 January 2021

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

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7 January 2021

The same prion strain causes vCJD and BSE

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7 January 2021

Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy

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7 January 2021

Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease

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7 January 2021

The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies

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7 January 2021

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

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7 January 2021

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

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7 January 2021

Restriction fragment length polymorphisms of the scrapie-associated fibril protein (PrP) gene and their association with susceptibility to natural scrapie in British sheep

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7 January 2021

Review: Creutzfeldt-Jakob disease

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7 January 2021

Epidemiological observations on spongiform encephalopathies in captive wild animals in the British Isles

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7 January 2021

Creutzfeldt-Jakob disease: a case with extensive white matter degeneration and optic atrophy

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7 January 2021

Cell-free formation of protease-resistant prion protein.

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7 January 2021

Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

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7 January 2021

Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker

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7 January 2021

Creutzfeldt-Jakob disease in mice: persistent viremia and preferential replication of virus in low-density lymphocytes.

1 reference

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7 January 2021

BSE transmission to macaques

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7 January 2021

The yeast [PSI+] prion: making sense of nonsense

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7 January 2021

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

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7 January 2021

Accidental transmission of Creutzfeldt-Jakob disease by dural cadaveric grafts

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7 January 2021

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

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7 January 2021

Prion protein conformation in a patient with sporadic fatal insomnia

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7 January 2021

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

1 reference

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7 January 2021

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

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7 January 2021

Spread of scrapie to sheep and goats by oral dosing with foetal membranes from scrapie-affected sheep

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7 January 2021

Further observations on the production of scrapie in sheep by oral dosing with foetal membranes from scrapie-affected sheep.

1 reference

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7 January 2021

Novel proteinaceous infectious particles cause scrapie

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7 January 2021

Not the last word on the BSE crisis

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7 January 2021

Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.

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7 January 2021

Clinical and genetic studies of fatal familial insomnia

1 reference

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7 January 2021

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene

1 reference

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7 January 2021

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

1 reference

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7 January 2021

First experimental transmission of fatal familial insomnia

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970169-9

7 January 2021

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970169-9

7 January 2021

Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970169-9

7 January 2021

A novel progressive spongiform encephalopathy in cattle

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https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970169-9

7 January 2021

Prions of yeast and fungi. Proteins as genetic material

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7 January 2021

Bovine spongiform encephalopathy: aspects of the clinical picture and analyses of possible changes 1986-1990

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7 January 2021

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

1 reference

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7 January 2021

10.1016/S0733-8619(05)70169-9

Identifiers

DOI

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29 July 2017

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