(Q34539307)

2 August 2017

title

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles (English)

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2 August 2017

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9

Prusiner SB

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2 August 2017

3

Farlow MR

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2 August 2017

Hsiao K

1

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2 August 2017

Dlouhy SR

2

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2 August 2017

Cass C

4

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2 August 2017

Da Costa M

5

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2 August 2017

Conneally PM

6

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2 August 2017

Hodes ME

7

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Ghetti B

8

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2 August 2017

language of work or name

English

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publication date

1 April 1992

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2 August 2017

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2 August 2017

volume

1

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2 August 2017

issue

1

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2 August 2017

page(s)

68-71

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

2 August 2017

cites work

1 reference

Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum.

21 January 2018

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

21 January 2018

1 reference

21 January 2018

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A protease-resistant protein is a structural component of the scrapie prion

21 January 2018

1 reference

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

Molecular cloning of a human prion protein cDNA

21 January 2018

1 reference

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

21 January 2018

1 reference

Inherited human prion diseases

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

21 January 2018

1 reference

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

21 January 2018

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Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

21 January 2018

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Genetics of prion infections

21 January 2018

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

21 January 2018

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Anticipating the anti-prion protein?

21 January 2018

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

21 January 2018

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Scrapie prions aggregate to form amyloid-like birefringent rods

21 January 2018

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Identification of prion amyloid filaments in scrapie-infected brain

21 January 2018

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Sleep apnea syndrome presenting with cognitive impairment

21 January 2018

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Observations on the brains of non-demented old people

21 January 2018

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Observations on the brains of demented old people

21 January 2018

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Formation of beta-amyloid protein deposits in brains of transgenic mice

21 January 2018

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Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

21 January 2018

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Mis-sense mutation Val&rarr;Ile in exon 17 of amyloid precursor protein gene in Japanese familial Alzheimer's disease

21 January 2018

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Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

21 January 2018

1 reference

21 January 2018

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Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Sträussler-Scheinker variant?).

21 January 2018

1 reference

7 January 2021

Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family

1 reference

7 January 2021

Gerstmann-Sträussler-Scheinker's disease. Electron-microscopic observations on a brain biopsy

1 reference

7 January 2021

Familial cerebral amyloidosis and spongiform encephalopathy

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7 January 2021

Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies

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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

Novel proteinaceous infectious particles cause scrapie

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7 January 2021

Prions and neurodegenerative diseases

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7 January 2021

Identification of a protein that purifies with the scrapie prion

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7 January 2021

Separation and properties of cellular and scrapie prion proteins

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7 January 2021

Assignment of the human and mouse prion protein genes to homologous chromosomes

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7 January 2021

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

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7 January 2021

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

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7 January 2021

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

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7 January 2021

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter

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7 January 2021

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

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7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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7 January 2021

Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein

1 reference

7 January 2021

Amyloid plaque core protein in Alzheimer disease and Down syndrome

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7 January 2021

Neuronal loss, neurofibrillary tangles and granulovacuolar degeneration in the hippocampus with ageing and dementia. A quantitative study

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7 January 2021

Deposits of Amyloid β Protein in the Central Nervous System of Transgenic Mice

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7 January 2021

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

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7 January 2021

Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination

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7 January 2021

Identifiers

DOI

10.1038/NG0492-68

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2 August 2017

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