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Neuropathology of hereditary forms of frontotemporal dementia and parkinsonism.
scientific article published on January 2008
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
Neuropathology of hereditary forms of frontotemporal dementia and parkinsonism
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
main subject
dementia
0 references
Parkinson's disease
1 reference
based on heuristic
inferred from title
frontotemporal dementia
1 reference
based on heuristic
inferred from title
author
David G. Munoz
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
author name string
Isidro Ferrer
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
publication date
1 January 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
published in
Handbook of clinical neurology / edited by P.J. Vinken and G.W. Bruyn
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
volume
89
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
page(s)
393-414
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
cites work
P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein.
1 reference
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A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notch.
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7 January 2021
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Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene
1 reference
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Crossref
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7 January 2021
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Molecular genetic characterisation of frontotemporal dementia on chromosome 3
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7 January 2021
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Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis.
1 reference
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7 January 2021
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The Effect of tau genotype on clinical features in FTDP-17
1 reference
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7 January 2021
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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
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7 January 2021
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Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia.
1 reference
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7 January 2021
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A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
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inferred from DOI database lookup
Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.
1 reference
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https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
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inferred from DOI database lookup
Argyrophilic grains: characteristic pathology of cerebral cortex in cases of adult onset dementia without Alzheimer changes
1 reference
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7 January 2021
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inferred from DOI database lookup
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial non-specific dementia maps to chromosome 3
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Crossref
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https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
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inferred from DOI database lookup
Familial dementia with swollen achromatic neurons and corticobasal inclusion bodies: a clinical and pathological study.
1 reference
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https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
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inferred from DOI database lookup
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
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inferred from DOI database lookup
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum
1 reference
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https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
CHMP2B mutations are not a common cause of frontotemporal lobar degeneration
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
1 reference
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https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Intranuclear rods and sheets in rat cochlear nucleus.
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Ubiquitin-negative mini-pick-like bodies in the dentate gyrus in p301l tauopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations causing neurodegenerative tauopathies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tau gene mutation in familial progressive subcortical gliosis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropsychiatric studies in a family with presenile dementia different from Alzheimer and Pick disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 3 linked frontotemporal dementia (FTD-3).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency oftau mutations in three series of non-Alzheimer's degenerative dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A distinct familial presenile dementia with a novel missense mutation in the tau gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pick-body-like inclusions in corticobasal degeneration differ from Pick bodies in Pick's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Another phenotype of frontotemporal dementia and parkinsonism linked to chromosome-17 (FTDP-17) with a missense mutation of S305N closely resembling Pick's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial frontotemporal dementia with a P301L tau mutation in Japan
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial progressive subcortical gliosis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frontotemporal dementia with novel tau pathology and a Glu342Valtau mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amyloid beta protein deposition in patients with frontotemporal lobar degeneration: relationship to age and apolipoprotein E genotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau pathology in a family with dementia and a P301L mutation in tau.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11-splice site in the tau gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of mutant and wild-type tau deposited in the brain affected by the FTDP-17 R406W mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetic and pathological classification of familial frontotemporal dementia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathologic, biochemical, and molecular characterization of the frontotemporal dementias
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Stains for the differential diagnosis of degenerative dementias
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The neuropathology and biochemistry of frontotemporal dementia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pick's disease associated with the novel Tau gene mutation K369I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An English kindred with a novel recessive tauopathy and respiratory failure.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau gene delN296 mutation, Parkinson's disease, and atypical supranuclear palsy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The tau R406W mutation causes progressive presenile dementia with bitemporal atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frontotemporal dementia with Pick-type histology associated with Q336R mutation in the tau gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau is a candidate gene for chromosome 17 frontotemporal dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The role of tau (MAPT) in frontotemporal dementia and related tauopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant dementia with widespread neurofibrillary tangles.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau gene mutation K257T causes a tauopathy similar to Pick's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive supranuclear palsy and Parkinson's disease in a family with a new mutation in the tau gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early-onset, rapidly progressive familial tauopathy with R406W mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Re-examination of a family with Pick's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The neuropathology of chromosome 17-linked dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau protein pathology in neurodegenerative diseases.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial frontotemporal dementia associated with a novel presenilin-1 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tubulin immunoreactive neuronal intranuclear inclusions in the human brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau protein in frontotemporal dementia linked to chromosome 3 (FTD-3).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau and alpha-synuclein inclusions in a case of familial frontotemporal dementia and progressive aphasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive nonfluent aphasia associated with a new mutation V363I in tau gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial amyotrophic lateral sclerosis with dementia: A second Canadian family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0072-9752%2807%2901237-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0072-9752(07)01237-7
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
PubMed ID
18631763
1 reference
stated in
Europe PubMed Central
PubMed ID
18631763
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18631763%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
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