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Neuropathology of frontotemporal lobar degeneration-tau (FTLD-tau).
scientific article published on July 2011
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Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
review article
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title
Neuropathology of frontotemporal lobar degeneration-tau (FTLD-tau)
(English)
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stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
author
Dennis W. Dickson
series ordinal
1
1 reference
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Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
N Kouri
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2
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stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
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6 February 2020
Melissa E. Murray
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3
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PMCID
3208128
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
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6 February 2020
author name string
Keith A Josephs
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4
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3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
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6 February 2020
publication date
1 July 2011
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Europe PubMed Central
PMCID
3208128
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
published in
Journal of Molecular Neuroscience
1 reference
stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
volume
45
1 reference
stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
page(s)
384-389
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Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
exact match
https://scigraph.springernature.com/pub.10.1007/s12031-011-9589-0
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Corticobasal degeneration: a pathologically distinct 4R tauopathy
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Does corticobasal degeneration exist? A clinicopathological re-evaluation
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Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
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Etiology and pathophysiology of frontotemporal dementia, Parkinson disease and Alzheimer disease: lessons from genetic studies
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J. Clifford Richardson and 50 years of progressive supranuclear palsy
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PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.
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27 July 2018
The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy
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Relative frequencies of Alzheimer disease, Lewy body, vascular and frontotemporal dementia, and hippocampal sclerosis in the State of Florida Brain Bank
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Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter
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Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease
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Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.
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Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration
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Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.
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Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
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Neuropathologic overlap of progressive supranuclear palsy, Pick's disease and corticobasal degeneration
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Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome.
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Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism
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26 September 2018
Identification of amino-terminally cleaved tau fragments that distinguish progressive supranuclear palsy from corticobasal degeneration.
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26 September 2018
Atrophy of superior cerebellar peduncle in progressive supranuclear palsy.
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26 September 2018
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26 September 2018
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.
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26 September 2018
Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease
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26 September 2018
Pathologic heterogeneity in clinically diagnosed corticobasal degeneration.
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26 September 2018
Progressive supranuclear palsy with dementia: cortical pathology.
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26 September 2018
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26 September 2018
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26 September 2018
Corticodentatonigral degeneration with neuronal achromasia: a progressive disorder of late adult life
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26 September 2018
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26 September 2018
Clinical and neuropathologic features of progressive supranuclear palsy with severe pallido-nigro-luysial degeneration and axonal dystrophy
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15 November 2018
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy
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15 November 2018
Phenotypes and prognosis: clinicopathologic studies of corticobasal degeneration
1 reference
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reference URL
https://pubmed.ncbi.nlm.nih.gov/21720721
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21720721
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21720721
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Parietal Pick's disease mimicking cortical-basal ganglionic degeneration
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21720721
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S12031-011-9589-0
1 reference
stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
PMCID
3208128
1 reference
stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
PubMed ID
21720721
1 reference
stated in
Europe PubMed Central
PMCID
3208128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21720721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
ResearchGate publication ID
51459154
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