Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease. - Wikidata - awgldk - TriplyDB

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease.

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease.

http://www.wikidata.org/entity/Q33615747

about

Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism.Precision medicine: Clarity for the clinical and biological complexity of Alzheimer's and Parkinson's diseases.Motor neuron disease-frontotemporal dementia: a clinical continuum.Intermediate C9orf72 alleles in neurological disorders: does size really matter?C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian population.

P2860

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P2860

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease.

http://www.wikidata.org/entity/Q33615747

description

2014 nî lūn-bûn

@nan

2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Absence of C9ORF72 expanded or ...... confirmed Parkinson's disease.

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Absence of C9ORF72 expanded or ...... confirmed Parkinson's disease.

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type

label

Absence of C9ORF72 expanded or ...... confirmed Parkinson's disease.

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Absence of C9ORF72 expanded or ...... confirmed Parkinson's disease.

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prefLabel

Absence of C9ORF72 expanded or ...... confirmed Parkinson's disease.

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Absence of C9ORF72 expanded or ...... confirmed Parkinson's disease.

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Movement Disorders

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Absence of C9ORF72 expanded or ...... confirmed Parkinson's disease.

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P2093

Deborah C Mash

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Eden R Martin

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Gary W Beecham

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Karen Nuytemans

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Lawrence S Honig

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Liyong Wang

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Matthew P Frosch

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Thomas J Montine

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Vanessa Inchausti

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Virginia M-Y Lee

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

P2860

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

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

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

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

Screening for C9orf72 repeat expansions in parkinsonian syndromes

Idiopathic Parkinson's disease phenotype related to C9ORF72 repeat expansions: contribution of the neuropsychological assessment.

Description of Parkinson's disease as a clinical syndrome.

Ecology of the aging human brain

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.

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827-830

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scholarly article

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10.1002/MDS.25838

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6

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29

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Jeffery M. Vance

Dennis W. Dickson

John Q. Trojanowski

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2014-02-26T00:00:00Z

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24573903

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P921

Parkinson's disease

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4022044

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