Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin (Q33984548)

30 July 2017

Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin (English)

1 reference

30 July 2017

0 references

1 reference

11

1 reference

30 July 2017

Glenn E Smith

13

0 references

Rosa Rademakers

series ordinal

7

object named as

Rosa Rademakers

1 reference

30 July 2017

14

Ronald C Petersen

1 reference

30 July 2017

6

David S Knopman

1 reference

30 July 2017

3

Bradley F Boeve

1 reference

30 July 2017

5

Maria Shiung

1 reference

30 July 2017

12

Joseph E Parisi

1 reference

30 July 2017

10

Karen M Kuntz

1 reference

30 July 2017

4

Matt Baker

1 reference

30 July 2017

1

Brendan J Kelley

1 reference

30 July 2017

2

Wael Haidar

1 reference

30 July 2017

Mike Hutton

8

1 reference

PubMed ID

20142525

30 July 2017

Jennifer Adamson

series ordinal

9

1 reference

30 July 2017

1 February 2010

1 reference

30 July 2017

Archives of Neurology

1 reference

30 July 2017

67

1 reference

30 July 2017

2

1 reference

30 July 2017

171-177

1 reference

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

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Clinically undetected motor neuron disease in pathologically proven frontotemporal lobar degeneration with motor neuron disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Mild cognitive impairment as a diagnostic entity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

A short test of mental status: description and preliminary results.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902004

Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20142525

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1001/ARCHNEUROL.2010.113

1 reference

30 July 2017

1 reference

30 July 2017

1 reference

PubMed ID

20142525