Progranulin and frontotemporal lobar degeneration - Wikidata - wikimedia - TriplyDB

Progranulin and frontotemporal lobar degeneration

Progranulin and frontotemporal lobar degeneration

http://www.wikidata.org/entity/Q28306543

about

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.Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration Eating disturbance in behavioural-variant frontotemporal dementia.Eating and hypothalamus changes in behavioral-variant frontotemporal dementia.TDP-43 functions within a network of hnRNP proteins to inhibit the production of a truncated human SORT1 receptor.The two faces of protein misfolding: gain- and loss-of-function in neurodegenerative diseases.Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.Association between progranulin and beta-amyloid in dementia with Lewy bodies.

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Progranulin and frontotemporal lobar degeneration

http://www.wikidata.org/entity/Q28306543

description

2007 nî lūn-bûn

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2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հուլիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Progranulin and frontotemporal lobar degeneration

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Progranulin and frontotemporal lobar degeneration

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Progranulin and frontotemporal lobar degeneration

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type

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Progranulin and frontotemporal lobar degeneration

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Progranulin and frontotemporal lobar degeneration

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Progranulin and frontotemporal lobar degeneration

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Progranulin and frontotemporal lobar degeneration

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Progranulin and frontotemporal lobar degeneration

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Progranulin and frontotemporal lobar degeneration

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S00401-007-0241-6

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Acta Neuropathologica

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Progranulin and frontotemporal lobar degeneration

@en

P2860

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

Cellular localization of gene expression for progranulin.

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

Tau gene mutation K257T causes a tauopathy similar to Pick's disease.

Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau

Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.

Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia.

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

Familial aggregation in frontotemporal dementia.

Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis.

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s00401-007-0241-6

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39-47

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scholarly article

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10.1007/S00401-007-0241-6

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1

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Stuart Pickering-Brown

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