Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria. (Q46130574)

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5 April 2020

title

Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria (English)

1 reference

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amyotrophic lateral sclerosis

5 April 2020

main subject

1 reference

3

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5 April 2020

Martin R. Turner

14

1 reference

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5 April 2020

Michael J Strong

1

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5 April 2020

Eneida Mioshi

7

1 reference

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5 April 2020

Angela C. Roberts

8

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5 April 2020

Julie Snowden

6

0 references

author name string

Sharon Abrahams

2

1 reference

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5 April 2020

Susan Woolley

4

1 reference

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5 April 2020

Paula Mclaughlin

5

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5 April 2020

Tibor HortobáGyi

10

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5 April 2020

Jeffrey Rosenfeld

11

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5 April 2020

Vincenzo Silani

12

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5 April 2020

Paul G Ince

13

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5 April 2020

Michael Benatar

9

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5 April 2020

publication date

5 January 2017

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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

5 April 2020

published in

1 reference

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5 April 2020

volume

18

1 reference

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5 April 2020

issue

3-4

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5 April 2020

page(s)

153-174

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28054827%20AND%20SRC:MED&resulttype=core&format=json

The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.

5 April 2020

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Cognition and eating behavior in amyotrophic lateral sclerosis: effect on survival

21 January 2018

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21 January 2018

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21 January 2018

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The Edinburgh Cognitive and Behavioural ALS Screen in a Chinese Amyotrophic Lateral Sclerosis Population

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21 January 2018

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Transcultural validation of the ALS-CBS Cognitive Section for the Brazilian population.

21 January 2018

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Cognitive impairment in ALS patients and validation of the Spanish version of the ALS-CBS test.

21 January 2018

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21 January 2018

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21 January 2018

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Integration of structural and functional magnetic resonance imaging in amyotrophic lateral sclerosis

21 January 2018

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Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions.

21 January 2018

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Multiparametric MRI study of ALS stratified for the C9orf72 genotype

21 January 2018

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Brain morphologic changes in asymptomatic C9orf72 repeat expansion carriers.

21 January 2018

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Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.

21 January 2018

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Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD).

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Stages of pTDP-43 pathology in amyotrophic lateral sclerosis

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Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

21 January 2018

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A harmonized classification system for FTLD-TDP pathology

21 January 2018

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Widespread neuronal and glial hyperphosphorylated tau deposition in ALS with cognitive impairment.

21 January 2018

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Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy

21 January 2018

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Spread of pathology in amyotrophic lateral sclerosis: assessment of phosphorylated TDP-43 along axonal pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

The cognitive and behavioural profile of amyotrophic lateral sclerosis: application of the consensus criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Spectrum of cognitive impairment in Korean ALS patients without known genetic mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Behavior matters--cognitive predictors of survival in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Sexual dimorphism in ALS: exploring gender-specific neuroimaging signatures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Dissection of genetic factors associated with amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

UBQLN2 variant of unknown significance in frontotemporal lobar degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Novel mutations support a role for Profilin 1 in the pathogenesis of ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Motor neuron involvement in multisystem proteinopathy: implications for ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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/10.1080%2F21678421.2016.1267768

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

TBK1 is associated with ALS and ALS-FTD in Sardinian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

The Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen: A cross-sectional comparison of established screening tools in a German-Swiss population

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

Longitudinal Changes in Discourse Prouction in Amyotrophic Lateral Sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F21678421.2016.1267768

The validation of El Escorial criteria for the diagnosis of amyotrophic lateral sclerosis: A clinicopathological study

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

National Institute of Neurological Disorders and Stroke-Canadian Stroke Network vascular cognitive impairment harmonization standards

1 reference

12 December 2020

Erratum to: Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD)

1 reference

12 December 2020

Discriminative and prognostic potential of cerebrospinal fluid phosphoTau/tau ratio and neurofilaments for frontotemporal dementia subtypes

1 reference

12 December 2020

TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts.

1 reference

12 December 2020

Detecting neurobehavioral changes in amyotrophic lateral sclerosis

1 reference

12 December 2020

Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers

1 reference

12 December 2020

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

1 reference

12 December 2020

Co-aggregation of RNA binding proteins in ALS spinal motor neurons: evidence of a common pathogenic mechanism

1 reference

12 December 2020

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

1 reference

12 December 2020

Deficits in emotional and social cognition in amyotrophic lateral sclerosis

1 reference

12 December 2020

Cognitive change in ALS: a prospective study

1 reference

12 December 2020

10.1080/21678421.2016.1267768

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28054827%20AND%20SRC:MED&resulttype=core&format=json

release_2c4hddp3kzbz5fbwgsu47otzqq

5 April 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2c4hddp3kzbz5fbwgsu47otzqq

24 November 2022

mapped directly with Wikidata item

0 references

1 reference