(Q36227050)

12 August 2017

0 references

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes (English)

1 reference

amyotrophic lateral sclerosis

12 August 2017

0 references

dementia

0 references

frontotemporal dementia

1 reference

21

1 reference

12 August 2017

O Mukherjee

12

0 references

Alison Goate

object named as

A Goate

13

0 references

John Anthony Hardy

23

object named as

J Hardy

1 reference

12 August 2017

8

A Chiò

1 reference

12 August 2017

J C Schymick

1

1 reference

12 August 2017

Y Yang

2

1 reference

12 August 2017

P M Andersen

3

1 reference

12 August 2017

J P Vonsattel

4

1 reference

12 August 2017

M Greenway

5

1 reference

12 August 2017

P Momeni

6

1 reference

12 August 2017

J Elder

7

1 reference

12 August 2017

G Restagno

9

1 reference

12 August 2017

W Robberecht

10

1 reference

12 August 2017

C Dahlberg

11

1 reference

12 August 2017

N Graff-Radford

14

1 reference

12 August 2017

R J Caselli

15

1 reference

12 August 2017

M Hutton

16

1 reference

12 August 2017

J Gass

17

1 reference

12 August 2017

A Cannon

18

1 reference

12 August 2017

R Rademakers

19

1 reference

12 August 2017

A B Singleton

20

1 reference

12 August 2017

J Rothstein

22

1 reference

12 August 2017

B J Traynor

24

1 reference

12 August 2017

language of work or name

English

0 references

publication date

19 March 2007

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

12 August 2017

1 reference

12 August 2017

78

1 reference

12 August 2017

754-756

1 reference

12 August 2017

7

1 reference

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

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

Are amyotrophic lateral sclerosis patients cognitively normal?

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

Amyotrophic lateral sclerosis and its association with dementia, parkinsonism and other neurological disorders: a review

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

Amyotrophic lateral sclerosis: current issues in classification, pathogenesis and molecular pathology.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117704

22 September 2018

Frontotemporal dementia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17371905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17371905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.2006.109553

1 reference

12 August 2017

1 reference

12 August 2017

1 reference