Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family (Q34472281)

2 August 2017

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family (English)

1 reference

amyotrophic lateral sclerosis

2 August 2017

0 references

1 reference

based on heuristic

inferred from title

amyotrophic lateral sclerosis and frontotemporal dementia

1 reference

22

Rosa Rademakers

1 reference

2 August 2017

21

Bruce L Miller

1 reference

2 August 2017

1

Adam L Boxer

1 reference

2 August 2017

5

William W Seeley

1 reference

2 August 2017

3

Bradley F Boeve

1 reference

2 August 2017

11

Jennifer Whitwell

1 reference

2 August 2017

Ian R Mackenzie

2

1 reference

2 August 2017

Matthew Baker

4

1 reference

2 August 2017

Richard Crook

6

1 reference

2 August 2017

Howard Feldman

7

1 reference

2 August 2017

Ging-Yuek R Hsiung

8

1 reference

2 August 2017

Nicola Rutherford

9

1 reference

2 August 2017

Victor Laluz

10

1 reference

2 August 2017

Dean Foti

12

1 reference

2 August 2017

Eric McDade

13

1 reference

2 August 2017

Jennifer Molano

14

1 reference

2 August 2017

Anna Karydas

15

1 reference

2 August 2017

Aleksandra Wojtas

16

1 reference

2 August 2017

Jill Goldman

17

1 reference

2 August 2017

Jacob Mirsky

18

1 reference

2 August 2017

Pheth Sengdy

19

1 reference

2 August 2017

Stephen Dearmond

20

1 reference

2 August 2017

language of work or name

English

0 references

publication date

20 June 2010

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

2 August 2017

1 reference

2 August 2017

82

1 reference

2 August 2017

196-203

1 reference

2 August 2017

2

1 reference

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Brain atrophy in primary lateral sclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

11C PiB and structural MRI provide complementary information in imaging of Alzheimer's disease and amnestic mild cognitive impairment

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Patterns of atrophy in pathologically confirmed FTLD with and without motor neuron degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Comparison of family histories in FTLD subtypes and related tauopathies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Frontotemporal dementia progresses to death faster than Alzheimer disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Survival in frontotemporal dementia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

The Clinical Dementia Rating (CDR): current version and scoring rules

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

Patterns of brain atrophy that differentiate corticobasal degeneration syndrome from progressive supranuclear palsy

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

A voxel-based morphometry study of patterns of brain atrophy in ALS and ALS/FTLD.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017222

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20562461

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20562461

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.2009.204081

1 reference

2 August 2017

1 reference

2 August 2017

1 reference