(Q38739503)

6 September 2017

Parkinsonism, movement disorders and genetics in frontotemporal dementia (English)

1 reference

6 September 2017

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frontotemporal dementia

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1 reference

parkinsonian syndrome

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2

Joseph Jankovic

1 reference

6 September 2017

José Fidel Baizabal-Carvallo

series ordinal

1

1 reference

PubMed ID

26891767

6 September 2017

language of work or name

English

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publication date

19 February 2016

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6 September 2017

Nature Reviews Neurology

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6 September 2017

12

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6 September 2017

3

1 reference

6 September 2017

175-185

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https://scigraph.springernature.com/pub.10.1038/nrneurol.2016.14

6 September 2017

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cites work

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Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management

21 January 2018

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Deciphering logopenic primary progressive aphasia: a clinical, imaging and biomarker investigation

21 January 2018

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Clinical aspects of familial forms of frontotemporal dementia associated with parkinsonism

21 January 2018

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Parkinsonian syndrome in familial frontotemporal dementia

21 January 2018

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Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Extrapyramidal signs, primitive reflexes and incontinence in fronto-temporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Extrapyramidal symptoms in Frontotemporal Dementia: prevalence and clinical correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Does corticobasal degeneration exist? A clinicopathological re-evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

"Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Criteria for the diagnosis of corticobasal degeneration

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Diagnostic criteria for corticobasal syndrome: a comparative study.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Neuropathology of variants of progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

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/10.1038%2FNRNEUROL.2016.14

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

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/10.1038%2FNRNEUROL.2016.14

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/10.1038%2FNRNEUROL.2016.14

The heritability and genetics of frontotemporal lobar degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A novel tau mutation, p.K317N, causes globular glial tauopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Phenotypic presentation of frontotemporal dementia with Parkinsonism‐chromosome 17 type P301S in a patient of Jewish‐Algerian origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The tau S305S mutation causes frontotemporal dementia with parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Prominent phenotypic variability associated with mutations in Progranulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Clinicopathologic correlation in PGRN mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Corticobasal syndrome associated with the A9D Progranulin mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Sortilin receptor 1 predicts longitudinal cognitive change

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Investigation of c9orf72 in 4 neurodegenerative disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Psychosis, C9ORF72 and dementia with Lewy bodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

C9ORF72 in dementia with Lewy bodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Differentiation of frontotemporal dementia from dementia with Lewy bodies using FP-CIT SPECT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Phenotypic variability in three families with valosin-containing protein mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Chromosome 9 ALS and FTD locus is probably derived from a single founder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Chromosome 3 linked frontotemporal dementia (FTD-3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The role of FUS gene variants in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frontotemporal dementia caused by CHMP2B mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Caudate atrophy on MRI is a characteristic feature of FTLD-FUS

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

TARDBP mutations in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The Met-allele of the BDNF Val66Met polymorphism enhances task switching in elderly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

No TARDBP mutations in a French Canadian population of patients with Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Mutational analysis of TARDBP in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Clearance of apoptotic neurons without inflammation by microglial triggering receptor expressed on myeloid cells-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy--PLOSL): a dementia associated with bone cystic lesions. From clinical to genetic and molecular aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

TREM2 Variants in Alzheimer's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Homozygous TREM2 mutation in a family with atypical frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

alpha-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The Stereotypy Rating Inventory for frontotemporal lobar degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The clinical spectrum of stereotypies in frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Stereotypies: a critical appraisal and suggestion of a clinically useful definition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Repetitive and compulsive behavior in frontal lobe degenerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Stereotypic behaviors in degenerative dementias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A study of the Lund-Manchester research criteria for frontotemporal dementia: clinical and single-photon emission CT correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer's disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A study of stereotypic behaviours in Alzheimer's disease and frontal and temporal variant frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Distinct behavioural profiles in frontotemporal dementia and semantic dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Efficacy of fluvoxamine as a treatment for behavioral symptoms in frontotemporal lobar degeneration patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Tetrabenazine for the treatment of chorea and other hyperkinetic movement disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Behavioral variant of frontotemporal dementia mimicking Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Progranulin gene mutation with an unusual clinical and neuropathologic presentation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Myoclonus and neurodegenerative disease--what's in a name?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A large Calabrian kindred segregating frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Exome sequencing identifies FUS mutations as a cause of essential tremor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

F-box only protein 7 gene in parkinsonian-pyramidal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

The impact of rare variants in FUS in essential tremor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Decline of cerebral glucose metabolism in frontotemporal dementia: a longitudinal 18F-FDG-PET-study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Subcortical and deep cortical atrophy in Frontotemporal Lobar Degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Caudate nucleus volumes in frontotemporal lobar degeneration: differential atrophy in subtypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Putaminal volume in frontotemporal lobar degeneration and Alzheimer disease: differential volumes in dementia subtypes and controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Patterns of striatal degeneration in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Striatal dopamine transporter and extrapyramidal symptoms in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Evaluation of dopaminergic function in frontotemporal dementia using I-FP-CIT single photon emission computed tomography.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Parkinsonism and impaired axonal transport in a mouse model of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Binge eating is associated with right orbitofrontal-insular-striatal atrophy in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Anatomic correlates of stereotypies in frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Imaging frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Plasma progranulin levels in cortical dementia phenotypes with asymmetric perisylvian atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

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/10.1038%2FNRNEUROL.2016.14

Genetics of frontotemporal lobar degeneration: an up-date and diagnosis algorithm

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Cerebrospinal Fluid Biomarkers in Familial Forms of Alzheimer's Disease and Frontotemporal Dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Exome sequencing in familial corticobasal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Imaging biomarkers in tauopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Mapping neuroinflammation in frontotemporal dementia with molecular PET imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

21 January 2018

Frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Clinical and Pathological Heterogeneity of Neuronal Intermediate Filament Inclusion Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

21 January 2018

Frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Juvenile frontotemporal dementia with parkinsonism associated with tau mutation G389R.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Investigation of C9orf72 repeat expansions in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Parkinson disease is not associated with C9ORF72 repeat expansions

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Mutational analysis of the VCP gene in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Different clinical and neuropathologic phenotypes of familial ALS with A315E TARDBP mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Tetrabenazine treatment for stereotypies and tics associated with dementia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Generalized myoclonus as a prominent symptom in a patient with FTLD-TDP

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Dystonia in corticobasal degeneration

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Evidence of Pre-Synaptic Dopaminergic Deficit in a Patient with a Novel Progranulin Mutation Presenting with Atypical Parkinsonism†

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Positron emission tomography in pallido-ponto-nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.14

KP1 expression of ghost Pick bodies, amyloid P-positive astrocytes and selective nigral degeneration in early onset Picks disease.

31 March 2020

1 reference

12 December 2020

18F-FDG PET findings in frontotemporal dementia: an SPM analysis of 29 patients.

1 reference

12 December 2020

The spectrum of recurrent thoughts and behaviors in frontotemporal dementia

1 reference

12 December 2020

Cerebral glucose metabolism in patients with frontotemporal dementia.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1038/NRNEUROL.2016.14

1 reference

PubMed ID

26891767

Dimensions Publication ID

6 September 2017

0 references

1 reference

PubMed ID

26891767