(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