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Cognitive and behavioral features of c9FTD/ALS
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PubMed
title
Cognitive and behavioral features of c9FTD/ALS
(English)
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PubMed
main subject
amyotrophic lateral sclerosis
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based on heuristic
litr
author
Bradley F Boeve
series ordinal
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object named as
Bradley F Boeve
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stated in
Crossref
Neill R Graff-Radford
series ordinal
2
object named as
Neill R Graff-Radford
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Crossref
language of work or name
English
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stated in
PubMed
publication date
2012
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PubMed
published in
Alzheimers Research & Therapy
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Crossref
volume
4
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PubMed
issue
4
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PubMed
page(s)
29
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PubMed
cites work
Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion
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Characterizing a neurodegenerative syndrome: primary progressive apraxia of speech
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Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics
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Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
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Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
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7 April 2017
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
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7 April 2017
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
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A harmonized classification system for FTLD-TDP pathology
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Classification of primary progressive aphasia and its variants
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The new classification of primary progressive aphasia into semantic, logopenic, or nonfluent/agrammatic variants
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7 April 2017
Cognition and anatomy in three variants of primary progressive aphasia
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7 April 2017
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
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7 April 2017
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
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7 April 2017
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
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7 April 2017
The neuropsychiatry of the cerebellum - insights from the clinic
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7 April 2017
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
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PubMed Central
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7 April 2017
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
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7 April 2017
Selective frontoinsular von Economo neuron and fork cell loss in early behavioral variant frontotemporal dementia
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PubMed Central
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7 April 2017
Selective functional, regional, and neuronal vulnerability in frontotemporal dementia
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PubMed Central
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7 April 2017
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
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https://api.crossref.org/works/10.1186/ALZRT132
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22 April 2017
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
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7 April 2017
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
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PubMed Central
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7 April 2017
Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria
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7 April 2017
Screening for C9ORF72 repeat expansion in FTLD.
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PubMed Central
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28 September 2017
Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion
1 reference
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PubMed Central
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28 September 2017
The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Repeat expansion in C9ORF72 in Alzheimer's disease
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PubMed Central
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28 September 2017
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
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28 September 2017
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p
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PubMed Central
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28 September 2017
The role of the cerebellum in cognition and emotion: personal reflections since 1982 on the dysmetria of thought hypothesis, and its historical evolution from theory to therapy
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28 September 2017
Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
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PubMed Central
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28 September 2017
Fluorodeoxyglucose F18 positron emission tomography in progressive apraxia of speech and primary progressive aphasia variants
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PubMed Central
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28 September 2017
Primary progressive aphasia: clinicopathological correlations
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PubMed Central
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28 September 2017
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.
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PubMed Central
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28 September 2017
Progressive aphasia secondary to Alzheimer disease vs FTLD pathology
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PubMed Central
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28 September 2017
The neuropathology of FTD associated With ALS.
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28 September 2017
Early frontotemporal dementia targets neurons unique to apes and humans
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28 September 2017
Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech
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PubMed Central
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28 September 2017
Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia
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PubMed Central
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28 September 2017
The cerebellar cognitive affective syndrome
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28 September 2017
An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.
1 reference
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PubMed Central
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31 May 2018
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.
1 reference
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Crossref
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21 January 2018
Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1186%2FALZRT132
retrieved
21 January 2018
Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1186%2FALZRT132
retrieved
21 January 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.
1 reference
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Crossref
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21 January 2018
Behavioural variant frontotemporal dementia: not all it seems?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1186%2FALZRT132
retrieved
21 January 2018
Combined magnetic resonance imaging and positron emission tomography brain imaging in behavioural variant frontotemporal degeneration: refining the clinical phenotype.
1 reference
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Crossref
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https://api.crossref.org/works/10.1186%2FALZRT132
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21 January 2018
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1186%2FALZRT132
retrieved
21 January 2018
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
1 reference
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Crossref
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https://api.crossref.org/works/10.1186%2FALZRT132
retrieved
21 January 2018
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
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1186%2FALZRT132
retrieved
21 January 2018
Ultrastructure of ubiquitin-positive, TDP-43-negative neuronal inclusions in cerebral cortex of C9ORF72-linked frontotemporal lobar degeneration/amyotrophic lateral sclerosis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506943
retrieved
28 November 2018
Identifiers
DOI
10.1186/ALZRT132
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Dimensions Publication ID
1052519199
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SciGraph
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9 September 2019
reference URL
https://scigraph.springernature.com/pub.10.1186/alzrt132
PMC publication ID
3506943
1 reference
stated in
PubMed
PubMed publication ID
22817642
1 reference
stated in
PubMed
ResearchGate publication ID
229433944
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