Clinical characterization of bvFTD due to FUS neuropathology. - Wikidata - awgldk - TriplyDB

Clinical characterization of bvFTD due to FUS neuropathology.

Clinical characterization of bvFTD due to FUS neuropathology.

http://www.wikidata.org/entity/Q30505752

about

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia Diagnosis and management of behavioral variant frontotemporal dementia Acute lesions that impair affective empathy.Neuroimaging in frontotemporal dementia.Neural substrates of socioemotional self-awareness in neurodegenerative disease.Longitudinal white matter changes in frontotemporal dementia subtypes.A clinicopathological approach to the diagnosis of dementia.Dynamical predictions of insular hubs for social cognition and their application to stroke.Self-Consciousness in Patients with Behavioral Variant Frontotemporal Dementia.Neuroimaging in Dementia.

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Clinical characterization of bvFTD due to FUS neuropathology.

http://www.wikidata.org/entity/Q30505752

description

2011 nî lūn-bûn

@nan

2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Clinical characterization of bvFTD due to FUS neuropathology.

@ast

Clinical characterization of bvFTD due to FUS neuropathology.

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type

label

Clinical characterization of bvFTD due to FUS neuropathology.

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Clinical characterization of bvFTD due to FUS neuropathology.

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prefLabel

Clinical characterization of bvFTD due to FUS neuropathology.

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Clinical characterization of bvFTD due to FUS neuropathology.

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Clinical characterization of bvFTD due to FUS neuropathology.

@en

P2093

Anna Karydas

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Christine M Stanley

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Pardis Poorzand

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Suzee E Lee

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P2860

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

A new subtype of frontotemporal lobar degeneration with FUS pathology

Voice processing in human and non-human primates.

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

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

FUS pathology in basophilic inclusion body disease

The functional neuroanatomy of the human orbitofrontal cortex: evidence from neuroimaging and neuropsychology

Neurodegenerative diseases target large-scale human brain networks

Cerebral processing of linguistic and emotional prosody: fMRI studies.

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

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Rosa Rademakers

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