(Q35043994)

6 August 2017

title

Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype (English)

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6 August 2017

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1

Suman Jayadev

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Bernardino F. Ghetti

7

object named as

Bernardino Ghetti

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6 August 2017

6

Thomas J Montine

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6 August 2017

David Nochlin

2

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6 August 2017

Parvoneh Poorkaj

3

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6 August 2017

Ellen J Steinbart

4

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6 August 2017

James A Mastrianni

5

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6 August 2017

Gerard D Schellenberg

8

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6 August 2017

Thomas D Bird

9

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6 August 2017

James B Leverenz

10

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6 August 2017

publication date

17 March 2011

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6 August 2017

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6 August 2017

volume

69

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6 August 2017

issue

4

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6 August 2017

page(s)

712-720

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Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Coexistence of Creutzfeldt-Jakob disease, Lewy body disease, and Alzheimer's disease pathology: an autopsy case showing typical clinical features of Creutzfeldt-Jakob disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Empiric refinement of the pathologic assessment of Lewy-related pathology in the dementia patient

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Neuropathological stageing of Alzheimer-related changes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114566

Validation of a short Orientation-Memory-Concentration Test of cognitive impairment.

8 July 2018

1 reference

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

21 January 2018

1 reference

A sporadic case of Creutzfeldt-Jakob disease with beta-amyloid deposits and alpha-synuclein inclusions

21 January 2018

1 reference

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

21 January 2018

1 reference

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

21 January 2018

1 reference

12 December 2020

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

1 reference

12 December 2020

Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165

1 reference

12 December 2020

Allelic origin of the abnormal prion protein isoform in familial prion diseases

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1002/ANA.22264

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6 August 2017

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6 August 2017

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