Frontotemporal lobar degeneration: current knowledge and future challenges. (Q38005348)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

title

Frontotemporal lobar degeneration: current knowledge and future challenges (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

frontotemporal lobar degeneration

29 January 2020

main subject

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

Chiara Cerami

1 reference

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29 January 2020

language of work or name

1 reference

25 April 2012

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29 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

volume

259

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29 January 2020

issue

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29 January 2020

page(s)

2278-2286

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

Behavioral features in semantic dementia vs other forms of progressive aphasias

29 January 2020

cites work

1 reference

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Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

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Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

21 January 2018

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Classification of primary progressive aphasia and its variants

21 January 2018

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Behavioural-variant frontotemporal dementia: diagnosis, clinical staging, and management

21 January 2018

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Progressive, isolated language disturbance: its significance in a 65-year-old-man. A case report with implications for treatment and review of literature

21 January 2018

1 reference

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Structural anatomy of empathy in neurodegenerative disease

21 January 2018

1 reference

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Cognition and anatomy in three variants of primary progressive aphasia

21 January 2018

1 reference

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The logopenic/phonological variant of primary progressive aphasia

21 January 2018

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Abeta amyloid and glucose metabolism in three variants of primary progressive aphasia

21 January 2018

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The prevalence of frontotemporal dementia

21 January 2018

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Epidemiology and genetics of frontotemporal dementia/Pick's disease.

21 January 2018

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Comparison of family histories in FTLD subtypes and related tauopathies

21 January 2018

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21 January 2018

Frontotemporal dementia

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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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/10.1007%2FS00415-012-6507-5

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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/10.1007%2FS00415-012-6507-5

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Tau gene mutations: dissecting the pathogenesis of FTDP-17.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

The role of tau (MAPT) in frontotemporal dementia and related tauopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Mutations causing neurodegenerative tauopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Tau Protein in Familial and Sporadic Diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Hereditary frontotemporal dementia caused by Tau gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Two distinct subtypes of right temporal variant frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Conversion of proepithelin to epithelins: roles of SLPI and elastase in host defense and wound repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

A harmonized classification system for FTLD-TDP pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Heterosexual pedophilia in a frontotemporal dementia patient with a mutation in the progranulin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Chromosome 3 linked frontotemporal dementia (FTD-3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Genetic contribution of FUS to frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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/10.1007%2FS00415-012-6507-5

Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon4 frequency, but no tau gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Apolipoprotein-E genotyping in Alzheimer's disease and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Apolipoprotein E polymorphism in patients with different neurodegenerative disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Apolipoprotein E gene and sporadic frontal lobe dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Apolipoprotein E polymorphism in German patients with frontotemporal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

The apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Frontotemporal dementia: clinicopathological correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Genetic evidence for the involvement of tau in progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Association of an extended haplotype in the tau gene with progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

GRN variability contributes to sporadic frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

UBAP1 is a component of an endosome-specific ESCRT-I complex that is essential for MVB sorting

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

A decade of genetic counseling in frontotemporal dementia affected families: few counseling requests and much familial opposition to testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

The effects of APOE and tau gene variability on risk of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Allele ε4 of Apolipoprotein E Shows a Dose Effect on Age at Onset of Pick Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-012-6507-5

Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis

21 January 2018

1 reference

12 December 2020

A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia

1 reference

12 December 2020

Differences in tau and apolipoprotein E polymorphism frequencies in sporadic frontotemporal lobar degeneration syndromes

1 reference

12 December 2020

The complex aetiology of frontotemporal lobar degeneration

1 reference

12 December 2020

From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder.

1 reference

12 December 2020

Patterns of cognitive and emotional empathy in frontotemporal lobar degeneration.

1 reference

12 December 2020

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

1 reference

12 December 2020

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

1 reference

12 December 2020

Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred

1 reference

12 December 2020

A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3

1 reference

12 December 2020

Cerebrospinal fluid biomarkers in Progranulin mutations carriers

1 reference

12 December 2020

BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease

1 reference

12 December 2020

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration

1 reference

12 December 2020

10.1007/S00415-012-6507-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 January 2020

1048918702

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22532172%20AND%20SRC:MED&resulttype=core&format=json