Three sib-pairs of autopsy-confirmed progressive supranuclear palsy (Q27304645)

25 June 2017

title

Three sib-pairs of autopsy-confirmed progressive supranuclear palsy (English)

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progressive supranuclear palsy

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8

Ryan J Uitti

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10

Zbigniew K Wszolek

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11

Rosa Rademakers

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9

Owen A Ross

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12

Dennis W Dickson

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7

Jay A van Gerpen

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3

Audrey J Strongosky

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1

Shinsuke Fujioka

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25 June 2017

Monica Sanchez-Contreras

series ordinal

2

object named as

Monica Y Sanchez Contreras

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4

Kotaro Ogaki

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6

Pawel M Tacik

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25 June 2017

author name string

Nathaniel Robb Whaley

series ordinal

5

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25 June 2017

language of work or name

English

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publication date

15 November 2014

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25 June 2017

number of pages

5

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Parkinsonism and Related Disorders

inferred from page(s)

published in

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volume

21

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issue

2

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page(s)

101-105

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

25 June 2017

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Neuropathology of variants of progressive supranuclear palsy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

The tauopathy associated with mutation 3 in intron 10 of Tau: characterization of the MSTD family

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

Tau exon 10 16 mutation FTDP-17 presenting clinically as sporadic young onset PSP.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306617

Progressive supranuclear palsy

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25443551

12 December 2020

inferred from PubMed ID database lookup

G303V tau mutation presenting with progressive supranuclear palsy-like features

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25443551

12 December 2020

inferred from PubMed ID database lookup

Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25443551

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/J.PARKRELDIS.2014.10.028

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25 June 2017

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