(Q47199003)

11 January 2018

title

The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype (English)

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11 January 2018

0 references

8

Liberski PP

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11 January 2018

author name string

Hainfellner JA

1

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11 January 2018

Brantner-Inthaler S

2

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11 January 2018

Cervenáková L

3

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11 January 2018

Brown P

4

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11 January 2018

Kitamoto T

5

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11 January 2018

Tateishi J

6

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11 January 2018

Diringer H

7

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11 January 2018

Regele H

9

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11 January 2018

Feucht M

10

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11 January 2018

publication date

1 July 1995

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11 January 2018

published in

Brain Pathology

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11 January 2018

volume

5

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11 January 2018

issue

3

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11 January 2018

page(s)

201-211

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11 January 2018

Spongiform encephalopathy transmitted experimentally from Creutzfeldt-Jakob and familial Gerstmann-Sträussler-Scheinker diseases.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Prion dementia without characteristic pathology

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Ballooned neurons in select neurodegenerative diseases contain phosphorylated neurofilament epitopes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.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.TB00596.X

An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.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.TB00596.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.TB00596.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Inherited human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

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

21 January 2018

1 reference

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Proteinase-resistant prion protein accumulation in Syrian hamster brain correlates with regional pathology and scrapie infectivity

21 January 2018

1 reference

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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.TB00596.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Molecular cloning of a human prion protein cDNA

21 January 2018

1 reference

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Gerstmann-Sträussler-Scheinker's disease

21 January 2018

1 reference

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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

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Dystrophic neurites around amyloid plaques of human patients with Gerstmann-Sträussler-Scheinker disease contain ubiquitinated inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

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

21 January 2018

1 reference

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Characterisation of antisera raised against species-specific peptide sequences from scrapie-associated fibril protein and their application for post-mortem immunodiagnosis of spongiform encephalopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

Molecular biology of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00596.X

10.1111/J.1750-3639.1995.TB00596.X

21 January 2018

Identifiers

DOI

1 reference

11 January 2018

release_xvcjrcsbofaqxp2liym67ul3eu

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/xvcjrcsbofaqxp2liym67ul3eu

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

8520719

1 reference

11 January 2018