(Q37228684)

English

Neurodegenerative disease phenotypes in carriers of MAPT p.A152T, a risk factor for frontotemporal dementia spectrum disorders and Alzheimer disease

scientific article published on October 2013

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scholarly article

1 reference

Europe PubMed Central

19 August 2017

Neurodegenerative disease phenotypes in carriers of MAPT p.A152T, a risk factor for frontotemporal dementia spectrum disorders and Alzheimer disease (English)

1 reference

Europe PubMed Central

19 August 2017

Alzheimer's disease

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neurodegeneration

1 reference

based on heuristic

inferred from title

frontotemporal dementia

1 reference

based on heuristic

inferred from title

Rosa Rademakers

10

object named as

Rosa Rademakers

1 reference

Europe PubMed Central

19 August 2017

Bruce L. Miller

22

object named as

Bruce L Miller

1 reference

Europe PubMed Central

19 August 2017

5

object named as

William W Seeley

1 reference

Europe PubMed Central

19 August 2017

15

object named as

Adam L Boxer

1 reference

Europe PubMed Central

19 August 2017

Gil D Rabinovici

19

object named as

Gil D Rabinovici

1 reference

Europe PubMed Central

19 August 2017

Daniel Geschwind

21

object named as

Daniel H Geschwind

1 reference

Europe PubMed Central

19 August 2017

Michael Geschwind

16

object named as

Michael D Geschwind

1 reference

Europe PubMed Central

19 August 2017

author name string

Suzee E Lee

1

1 reference

Europe PubMed Central

19 August 2017

Maria C Tartaglia

2

1 reference

Europe PubMed Central

19 August 2017

Görsev Yener

3

1 reference

Europe PubMed Central

19 August 2017

Sermin Genç

4

1 reference

Europe PubMed Central

19 August 2017

Pascual Sanchez-Juan

6

1 reference

Europe PubMed Central

19 August 2017

Fermin Moreno

7

1 reference

Europe PubMed Central

19 August 2017

Mario F Mendez

8

1 reference

Europe PubMed Central

19 August 2017

Eric Klein

9

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Europe PubMed Central

19 August 2017

Adolfo López de Munain

11

1 reference

Europe PubMed Central

19 August 2017

Onofre Combarros

12

1 reference

Europe PubMed Central

19 August 2017

Joel H Kramer

13

1 reference

Europe PubMed Central

19 August 2017

Robert O Kenet

14

1 reference

Europe PubMed Central

19 August 2017

Maria-Luisa Gorno-Tempini

17

1 reference

Europe PubMed Central

19 August 2017

Anna M Karydas

18

1 reference

Europe PubMed Central

19 August 2017

Giovanni Coppola

20

1 reference

Europe PubMed Central

19 August 2017

language of work or name

0 references

publication date

1 October 2013

1 reference

Europe PubMed Central

19 August 2017

Alzheimer Disease and Associated Disorders

1 reference

Europe PubMed Central

19 August 2017

27

1 reference

Europe PubMed Central

19 August 2017

302-309

1 reference

Europe PubMed Central

19 August 2017

4

1 reference

Europe PubMed Central

19 August 2017

The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Classification of primary progressive aphasia and its variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Temporoparietal atrophy: a marker of AD pathology independent of clinical diagnosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Abeta amyloid and glucose metabolism in three variants of primary progressive aphasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Frontotemporal dementia: clinicopathological correlations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Clinicopathological correlates in frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Cognition and anatomy in three variants of primary progressive aphasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Distinctive neuropsychological patterns in frontotemporal dementia, semantic dementia, and Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy brain bank

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Accuracy of the clinical diagnosis of corticobasal degeneration: a clinicopathologic study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

The Clinical Dementia Rating (CDR): current version and scoring rules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

6 September 2017

The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

14 September 2017

The structural basis of monoclonal antibody Alz50's selectivity for Alzheimer's disease pathology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

26 June 2018

Unclassifiable tauopathy associated with an A152T variation in MAPT exon 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

3 September 2018

The 10-word learning task in the differential diagnosis of early Alzheimer's disease and elderly depression: A cross-sectional pilot study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

3 September 2018

Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

3 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

3 September 2018

Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

3 September 2018

Pathologic heterogeneity in clinically diagnosed corticobasal degeneration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3796183

3 September 2018

Procerus sign in progressive supranuclear palsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23518664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics: The MAPT locus-a genetic paradigm in disease susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/23518664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/WAD.0B013E31828CC357

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

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