Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study (Q35859698)

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scientific article published on 3 February 2012

Language	Label	Description	Also known as
English	Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study	scientific article published on 3 February 2012

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scholarly article

1 reference

Europe PubMed Central

10 August 2017

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study (English)

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Europe PubMed Central

10 August 2017

amyotrophic lateral sclerosis

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Daniel G. Bradley

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10 August 2017

Russell McLaughlin

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Russell L McLaughlin

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Susan Byrne

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Aleksey Shatunov

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Aleksey Shatunov

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Niall P. Pender

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Niall Pender

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Cathal Walsh

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Ammar Al-Chalabi

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Ammar Al-Chalabi

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Mark Heverin

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Europe PubMed Central

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Peter Bede

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Europe PubMed Central

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Marwa Elamin

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Parameswaran Mahadeva Iyer

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Parameswaran Mahadeva Iyer

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Brona Wynne

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Bernie Corr

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Norah Jordan

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Kevin Kenna

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Catherine Lynch

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Catherine Lynch

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Julie Phukan

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Arun L Bokde

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Europe PubMed Central

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author name string

Caoimhe O'Brien

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publication date

3 February 2012

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Europe PubMed Central

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Lancet Neurology

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Europe PubMed Central

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11

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232-240

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3

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10 August 2017

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.

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27 July 2018

Clinical diagnosis and management of amyotrophic lateral sclerosis

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27 July 2018

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

27 July 2018

Chromosome 9 ALS and FTD locus is probably derived from a single founder

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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

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27 July 2018

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

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27 July 2018

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

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Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

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Voxel-based morphometry–the methods

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27 July 2018

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

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Genetic family history questionnaire

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27 July 2018

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Neurobehavioral symptoms in ALS are negatively related to caregivers' burden and quality of life.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Neural correlates of distance and congruity effects in a numerical Stroop task: an event-related fMRI study

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24 September 2018

Word retrieval in amyotrophic lateral sclerosis: a functional magnetic resonance imaging study.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Executive control function: a review of its promise and challenges for clinical research. A report from the Committee on Research of the American Neuropsychiatric Association.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Assessing frontal lobe behavioral syndromes with the frontal lobe personality scale.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Incidence and prevalence of ALS in Ireland, 1995-1997: a population-based study.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

24 September 2018

Proposed criteria for familial amyotrophic lateral sclerosis

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315021

6 December 2018

Absence of consensus in diagnostic criteria for familial neurodegenerative diseases

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https://pubmed.ncbi.nlm.nih.gov/22305801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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https://pubmed.ncbi.nlm.nih.gov/22305801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S1474-4422(12)70014-5

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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