(Q37254394)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

title

The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

13 January 2020

main subject

0 references

author

Michael J Strong

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

author name string

Michael J Strong

series ordinal

1

1 reference

19 August 2017

publication date

1 December 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

13 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

page(s)

323-338

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

Motor neurone disease, dementia and aphasia: coincidence, co-occurrence or continuum?

13 January 2020

cites work

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21 January 2018

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21 January 2018

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Are amyotrophic lateral sclerosis patients cognitively normal?

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Prevalence and patterns of cognitive impairment in sporadic ALS.

21 January 2018

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Frontotemporal dementia progresses to death faster than Alzheimer disease

21 January 2018

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Rate of progression differs in frontotemporal dementia and Alzheimer disease.

21 January 2018

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The effects of executive and behavioral dysfunction on the course of ALS.

21 January 2018

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Alzheimer disease and frontotemporal dementias. Behavioral distinctions

21 January 2018

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Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

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Rapidly progressive aphasic dementia and motor neuron disease

21 January 2018

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Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis. A longitudinal study in 52 patients.

21 January 2018

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Neuropsychological, electroencephalogram and brain computed tomography findings in motor neuron disease.

21 January 2018

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Neuropsychological dysfunctions in amyotrophic lateral sclerosis: relation to motor disabilities.

21 January 2018

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Frontal lobe function in amyotrophic lateral sclerosis: a neuropsychologic and positron emission tomography study

21 January 2018

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Cognition, language, and speech in amyotrophic lateral sclerosis: a review.

21 January 2018

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Selective impairment of verb processing associated with pathological changes in Brodmann areas 44 and 45 in the motor neurone disease-dementia-aphasia syndrome.

21 January 2018

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Frontal lobe dementia and motor neuron disease

21 January 2018

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The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

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Focal reductions of cerebral blood flow in amyotrophic lateral sclerosis: a [99mTc]-d,l-HMPAO SPECT study

21 January 2018

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The relationship between abnormalities of cognitive function and cerebral activation in amyotrophic lateral sclerosis. A neuropsychological and positron emission tomography study.

21 January 2018

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Neuronal loss associated with cognitive performance in amyotrophic lateral sclerosis: an (11C)-flumazenil PET study

21 January 2018

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Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis: an [11C](R)-PK11195 positron emission tomography study.

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

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TDP-43 A315T mutation in familial motor neuron disease

21 January 2018

1 reference

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

21 January 2018

1 reference

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The central nervous system in motor neurone disease

21 January 2018

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Characterization of neuronal intermediate filament protein expression in cervical spinal motor neurons in sporadic amyotrophic lateral sclerosis (ALS).

21 January 2018

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Neurofilament metabolism in sporadic amyotrophic lateral sclerosis.

21 January 2018

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Sporadic amyotrophic lateral sclerosis with extensive neurological involvement

21 January 2018

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Tau protein aggregation in the frontal and entorhinal cortices as a function of aging.

21 January 2018

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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

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TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

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Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9

21 January 2018

1 reference

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Structural diversity and functional implications of the eukaryotic TDP gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

21 January 2018

1 reference

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Higher order arrangement of the eukaryotic nuclear bodies

21 January 2018

1 reference

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TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein

21 January 2018

1 reference

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TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

21 January 2018

1 reference

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Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

21 January 2018

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Frontotemporal lobar degeneration: clinical and pathological relationships

21 January 2018

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

21 January 2018

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TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation

21 January 2018

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TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations

21 January 2018

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Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases

21 January 2018

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A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology

21 January 2018

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Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion.

21 January 2018

1 reference

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The neuropathology and clinical phenotype of FTD with progranulin mutations

21 January 2018

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Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43.

21 January 2018

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Lowered cerebral glucose utilization in amyotrophic lateral sclerosis

21 January 2018

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Evidence for a dopaminergic deficit in sporadic amyotrophic lateral sclerosis on positron emission scanning

21 January 2018

1 reference

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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%2F17482960802372371

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%2F17482960802372371

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

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%2F17482960802372371

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%2F17482960802372371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

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%2F17482960802372371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

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%2F17482960802372371

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%2F17482960802372371

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

A positron emission tomography study of frontal lobe function (verbal fluency) in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802372371

10.1080/17482960802372371

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18752088%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

1 reference