(Q40625739)

22 September 2017

1 reference

title

Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles (English)

1 reference

22 September 2017

G Giaccone

3

1 reference

ORCID Public Data File 2021

Martin R. Farlow

6

object named as

M R Farlow

1 reference

22 September 2017

B Ghetti

1

1 reference

22 September 2017

F Tagliavini

2

1 reference

22 September 2017

O Bugiani

4

1 reference

22 September 2017

B Frangione

5

1 reference

22 September 2017

S R Dlouhy

7

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22 September 2017

publication date

1 February 1994

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22 September 2017

published in

Molecular Neurobiology

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22 September 2017

volume

8

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22 September 2017

issue

1

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22 September 2017

page(s)

41-48

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

22 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF02778006

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/10.1007%2FBF02778006

Inherited human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02778006

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02778006

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

21 January 2018

1 reference

12 December 2020

Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.

1 reference

12 December 2020

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

1 reference

12 December 2020

Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58

1 reference

12 December 2020

Identification of a protein that purifies with the scrapie prion.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Abnormal Eye Movements in Gerstmann-Sträussler-Scheinker Disease

1 reference

12 December 2020

Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies

1 reference

12 December 2020

Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred

1 reference

12 December 2020

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

1 reference

12 December 2020

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

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/BF02778006

1 reference

Dimensions Publication ID

22 September 2017

1046716753

0 references

1 reference