(Q21261387)

17 August 2022

John Hardy

John

Hardy

1 reference

17 August 2022

Stuart Pickering-Brown

object named as

Stuart Pickering-Brown

Stuart

Pickering-Brown

1 reference

17 August 2022

Adriano Chiò

Adriano

Chiò

1 reference

17 August 2022

Ekaterina Rogaeva

Ekaterina

Rogaeva

1 reference

17 August 2022

Elisa Greggio

Elisa

Greggio

1 reference

Peter Henry St George-Hyslop

17 August 2022

object named as

Peter St George-Hyslop

Peter

St George-Hyslop

1 reference

17 August 2022

Jordan Grafman

Jordan

Grafman

1 reference

17 August 2022

Orla Hardiman

Orla

Hardiman

1 reference

17 August 2022

David M Holtzman

David M

Holtzman

1 reference

17 August 2022

Parastoo Momeni

Parastoo

Momeni

1 reference

17 August 2022

Mark R Cookson

Mark R

Cookson

1 reference

17 August 2022

Bryan J Traynor

Bryan J

Traynor

1 reference

17 August 2022

Nigel J Cairns

Nigel J

Cairns

1 reference

17 August 2022

Edward D

Huey

Edward D Huey

1 reference

17 August 2022

Eric M

Wassermann

Eric M Wassermann

1 reference

17 August 2022

Jeffrey D Rothstein

Jeffrey D

Rothstein

1 reference

17 August 2022

Jennifer Schymick

Jennifer

Schymick

1 reference

17 August 2022

Shushant Jain

Shushant

Jain

1 reference

17 August 2022

Matthew J Greenway

Matthew J

Greenway

1 reference

17 August 2022

Stephen Berger

Stephen

Berger

1 reference

17 August 2022

Hon Chung Fung

Hon Chung

Fung

1 reference

17 August 2022

Jennifer Adamson

Jennifer

Adamson

1 reference

17 August 2022

Michael L Hutton

Michael L

Hutton

1 reference

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

17 August 2022

language of work or name

English

0 references

publication date

2006

0 references

0 references

0 references

0 references

0 references

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

A human genome diversity cell line panel

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

Amyotrophic lateral sclerosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

Are amyotrophic lateral sclerosis patients cognitively normal?

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

The road less traveled: emerging principles of kinesin motor utilization

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

Inheritance of frontotemporal dementia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

30 May 2018

Frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-6-44

Genetic Variability in CHMP2B and Frontotemporal Dementia

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764752

Cognitive impairment in sporadic ALS: a pathologic continuum underlying a multisystem disorder

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17166276

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17166276

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2377-6-44

0 references