(Q38922949)

7 September 2017

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation (English)

1 reference

7 September 2017

Corticobasal syndrome

1 reference

8

Rosa Rademakers

1 reference

7 September 2017

5

Rick van Minkelen

1 reference

7 September 2017

Elise G P Dopper

1

1 reference

7 September 2017

Harro Seelaar

2

1 reference

7 September 2017

Wang Zheng Chiu

3

1 reference

7 September 2017

Inge de Koning

4

1 reference

7 September 2017

Matthew C Baker

6

1 reference

7 September 2017

Annemieke J M Rozemuller

7

1 reference

7 September 2017

John C van Swieten

9

1 reference

7 September 2017

24 August 2011

1 reference

Journal of Molecular Neuroscience

7 September 2017

1 reference

7 September 2017

45

1 reference

7 September 2017

3

1 reference

7 September 2017

354-358

1 reference

https://scigraph.springernature.com/pub.10.1007/s12031-011-9626-z

7 September 2017

0 references

cites work

Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Imaging correlates of pathology in corticobasal syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Symmetric corticobasal degeneration (S-CBD).

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Sporadic corticobasal syndrome due to FTLD-TDP.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Gene expression study on peripheral blood identifies progranulin mutations

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

The many faces of corticobasal degeneration

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Prominent phenotypic variability associated with mutations in Progranulin

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Distinct genetic forms of frontotemporal dementia.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Serum biomarker for progranulin-associated frontotemporal lobar degeneration

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Corticobasal syndrome associated with the A9D Progranulin mutation

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

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

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Automated extraction and amplification of DNA from whole blood using a robotic workstation and an integrated thermocycler.

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Pathologic heterogeneity in clinically diagnosed corticobasal degeneration

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207131

Progranulin null mutations in both sporadic and familial frontotemporal dementia

22 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21863316

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Low Serum Progranulin Predicts the Presence of Mutations: A Prospective Study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21863316

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S12031-011-9626-Z

1 reference

Dimensions Publication ID

7 September 2017

1015248896

0 references

Fatcat ID

release_bx44gleckrawxdxijqjfety2cu

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/bx44gleckrawxdxijqjfety2cu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

7 September 2017

PubMed publication ID

21863316

1 reference