(Q35883188)

10 August 2017

Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin (English)

1 reference

10 August 2017

0 references

5

K Kantarci

1 reference

10 August 2017

9

D Knopman

1 reference

10 August 2017

13

R Petersen

1 reference

10 August 2017

7

V J Lowe

1 reference

10 August 2017

2

B F Boeve

1 reference

10 August 2017

E McDade

1

1 reference

10 August 2017

T M Burrus

3

1 reference

10 August 2017

B P Boot

4

1 reference

10 August 2017

J Fields

6

1 reference

10 August 2017

P Peller

8

1 reference

10 August 2017

M Baker

10

1 reference

10 August 2017

N Finch

11

1 reference

10 August 2017

R Rademakers

12

1 reference

10 August 2017

language of work or name

English

0 references

publication date

4 April 2012

1 reference

10 August 2017

1 reference

10 August 2017

78

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10 August 2017

16

1 reference

10 August 2017

1245-1249

1 reference

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

Prominent phenotypic variability associated with mutations in Progranulin

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

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

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

Corticobasal Degeneration and Frontotemporal Dementia Presentations in a Kindred with Nonspecific Histopathology

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324318

A diagnostic approach in Alzheimer's disease using three-dimensional stereotactic surface projections of fluorine-18-FDG PET

6 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22491866

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/WNL.0B013E318251594C

1 reference

10 August 2017

1 reference

10 August 2017

PubMed publication ID

22491866

1 reference