Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features - Wikidata - awgldk - TriplyDB

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

http://www.wikidata.org/entity/Q36198642

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Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia Diagnosis and management of behavioral variant frontotemporal dementia Neuroimaging biomarkers of neurodegenerative diseases and dementia Frontotemporal dementia: a bridge between dementia and neuromuscular disease C9orf72-related disorders: expanding the clinical and genetic spectrum of neurodegenerative diseases Frontotemporal Dementia.Dementia and neuroimaging.Psychosis and hallucinations in frontotemporal dementia with the C9ORF72 mutation: a detailed clinical cohort Early-onset Alzheimer's disease versus frontotemporal dementia: resolution with genetic diagnoses?Psychiatric Aspects of Dementia.Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype.Neuroimaging in frontotemporal dementia.Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images.The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis.Psychotic symptoms in frontotemporal dementia: a diagnostic dilemma?The Phenotype of the C9ORF72 Expansion Carriers According to Revised Criteria for bvFTD.Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers.Advances in neuroimaging in frontotemporal dementia.Neural basis of motivational approach and withdrawal behaviors in neurodegenerative disease.Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers.Amyloid in dementia associated with familial FTLD: not an innocent bystander.Frontotemporal Dementia and Psychiatric Illness: Emerging Clinical and Biological Links in Gene Carriers.Neuroimaging features of C9ORF72 expansion Non-pharmacological Management of Behavioral Symptoms in Frontotemporal and Other Dementias.Frontotemporal dementia: diagnosis, deficits and management Dissociation of Structural and Functional Integrities of the Motor System in Amyotrophic Lateral Sclerosis and Behavioral-Variant Frontotemporal Dementia.Neural substrates of episodic memory dysfunction in behavioural variant frontotemporal dementia with and without C9ORF72 expansions Diagnostic utility of ASL-MRI and FDG-PET in the behavioral variant of FTD and AD.Spectrum of cognitive impairment in Korean ALS patients without known genetic mutations Neuropsychiatric features of C9orf72-associated behavioral variant frontotemporal dementia and frontotemporal dementia with motor neuron disease.Treatment implications of C9ORF72.The behavioral variant of frontotemporal dementia: linking neuropathology to social cognition.C9ORF72 mutations in neurodegenerative diseases.The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issues.C9ORF72 hexanucleotide repeats in behavioral and motor neuron disease: clinical heterogeneity and pathological diversity.Neuropsychological Profile in the C9ORF72 Associated Behavioral Variant Frontotemporal Dementia.

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Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

http://www.wikidata.org/entity/Q36198642

description

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

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Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

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Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

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Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

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prefLabel

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

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Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

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Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

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Anna Karydas

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Baber Khan

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Daniel H Geschwind

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Giovanni Coppola

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Jamie C Fong

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Jennifer S Yokoyama

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Leonel T Takada

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Matt C Baker

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Mochtar Pribadi

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Nicola J Rutherford

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P2860

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

A harmonized classification system for FTLD-TDP pathology

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

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

The neural basis of surface dyslexia in semantic dementia

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

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

Validation of the new interpretive guidelines for the clinical dementia rating scale sum of boxes score in the national Alzheimer's coordinating center database.

The prevalence of frontotemporal dementia.

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Rosa Rademakers

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Katherine P Rankin

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