Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation. - Wikidata - awgldk - TriplyDB

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

http://www.wikidata.org/entity/Q38922949

about

Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism.Novel GRN Mutations in Patients with Corticobasal Syndrome "Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations.Visual signs and symptoms of corticobasal degeneration.Circulating progranulin as a biomarker for neurodegenerative diseases Transcriptional profiling of chronic clinical hepatic schistosomiasis japonica indicates reduced metabolism and immune responses.Pathology and sensitivity of current clinical criteria in corticobasal syndrome.Investigating the neuroanatomical substrate of pathological laughing and crying in amyotrophic lateral sclerosis with multimodal neuroimaging techniques.

P2860

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P2860

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

http://www.wikidata.org/entity/Q38922949

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

@wuu

2011年学术文章

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2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

2011年學術文章

@zh

2011年學術文章

@zh-hant

name

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

@en

type

label

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

@en

prefLabel

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

@en

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P1433

Journal of Molecular Neuroscience

P1476

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

@en

P2093

Annemieke J M Rozemuller

http://www.w3.org/2001/XMLSchema#string

Elise G P Dopper

http://www.w3.org/2001/XMLSchema#string

Harro Seelaar

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Inge de Koning

http://www.w3.org/2001/XMLSchema#string

John C van Swieten

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Matthew C Baker

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Rick van Minkelen

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Wang Zheng Chiu

http://www.w3.org/2001/XMLSchema#string

P2860

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

Sporadic corticobasal syndrome due to FTLD-TDP.

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

The many faces of corticobasal degeneration.

Symmetric corticobasal degeneration (S-CBD).

Imaging correlates of pathology in corticobasal syndrome.

TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia.

Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia.

Prominent phenotypic variability associated with mutations in Progranulin

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s12031-011-9626-z

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354-358

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scholarly article

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10.1007/S12031-011-9626-Z

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3

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Rosa Rademakers

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51591912

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