Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family (Q28301715)

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English	Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family	scientific article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

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frontotemporal dementia

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

Giuseppe Di Fede

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Fabrizio Tagliavini

6

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

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Anna Rita Giovagnoli

1

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17 January 2020

Anna Aresi

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Fabiola Reati

4

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17 January 2020

Giacomina Rossi

5

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17 January 2020

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publication date

21 November 2008

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17 January 2020

Neurological Sciences

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17 January 2020

29

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17 January 2020

6

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17 January 2020

405-410

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Prion disease (PrP-A117V) presenting with ataxia instead of dementia

1 reference

https://api.crossref.org/works/10.1007%2FS10072-008-1025-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10072-008-1025-Z

21 January 2018

A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-008-1025-Z

21 January 2018

Specific impairments of planning

1 reference

https://api.crossref.org/works/10.1007%2FS10072-008-1025-Z

21 January 2018

Cognitive planning deficit in patients with cerebellar atrophy.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-008-1025-Z

21 January 2018

Memory in patients with cerebellar degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS10072-008-1025-Z

21 January 2018

Raven's coloured progressive matrices: normative values on 305 adult normal controls

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gerstmann-Sträussler-Scheinker disease and the Indiana kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imitating gestures. A quantitative approach to ideomotor apraxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana kindred (F198S).

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gerstmann-Sträussler-Scheinker disease with the Q217R mutation mimicking frontotemporal dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the prion protein gene phenotypic spectrum

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The token test: A sensitive test to detect receptive disturbances in aphasics

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary prion protein amyloidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of progranulin function in frontotemporal lobar degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19030774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10072-008-1025-Z

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19030774%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

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