(Q48656137)

13 February 2018

title

The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease. (English)

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13 February 2018

author name string

P Brown

1

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13 February 2018

L G Goldfarb

2

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13 February 2018

C J Gibbs

3

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13 February 2018

D C Gajdusek

4

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13 February 2018

publication date

1 September 1991

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13 February 2018

European Journal of Epidemiology

published in

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13 February 2018

volume

7

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13 February 2018

issue

5

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13 February 2018

page(s)

469-476

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13 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00143124

exact match

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cites work

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00143124

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

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease.

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12 December 2020

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

1 reference

12 December 2020

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families

1 reference

12 December 2020

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

12 December 2020

Clinical and molecular genetic study of a large German kindred with Gerstmann-Straussler-Scheinker syndrome

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12 December 2020

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families

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12 December 2020

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome

1 reference

12 December 2020

Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

1 reference

12 December 2020

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

12 December 2020

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

1 reference

12 December 2020

[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease]

1 reference

12 December 2020

Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases.

1 reference

12 December 2020

The molecular genetics of familial Creutzfeldt-Jakob disease in France

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis

1 reference

12 December 2020

Prion dementia without characteristic pathology

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00143124

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13 February 2018

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13 February 2018