In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17. (Q33678388)

28 July 2017

In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17. (English)

1 reference

Frontotemporal dementia and parkinsonism linked to chromosome 17

28 July 2017

0 references

Parkinson's disease

1 reference

based on heuristic

inferred from title

frontotemporal dementia

1 reference

based on heuristic

inferred from title

parkinsonian syndrome

1 reference

Pietro Pietrini

5

0 references

Jordan Grafman

10

object named as

Jordan Grafman

1 reference

28 July 2017

1

Bernardino Ghetti

1 reference

28 July 2017

4

Edward D Huey

1 reference

28 July 2017

3

Jill R Murrell

1 reference

28 July 2017

9

Martin R Farlow

1 reference

28 July 2017

Salvatore Spina

2

1 reference

28 July 2017

Brian Sweeney

6

1 reference

28 July 2017

Eric M Wassermann

7

1 reference

28 July 2017

Catherine Keohane

8

1 reference

28 July 2017

6 March 2008

1 reference

Neurodegenerative Diseases

28 July 2017

1 reference

28 July 2017

5

1 reference

28 July 2017

3-4

1 reference

28 July 2017

215-217

1 reference

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

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Hereditary frontotemporal dementia caused by Tau gene mutations.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Corticobasal syndrome associated with the A9D Progranulin mutation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

The novel Tau mutation G335S: clinical, neuropathological and molecular characterization.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826454

30 October 2018

Identifiers

DOI

10.1159/000113706

1 reference

28 July 2017

1 reference

28 July 2017

1 reference