Large C9orf72 repeat expansions are not a common cause of Parkinson's disease. - Wikidata - awgldk - TriplyDB

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

http://www.wikidata.org/entity/Q35984663

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C9orf72 repeat expansions are a rare genetic cause of parkinsonism C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies From animal models to human disease: a genetic approach for personalized medicine in ALS Frontotemporal dementia: a bridge between dementia and neuromuscular disease Lack of c9orf72 repeat expansion in taiwanese patients with mixed neurodegenerative disorders Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease.The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype.Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.Parkinson disease is not associated with C9ORF72 repeat expansions.Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease.Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72.TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia.How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?C9ORF72 mutations in neurodegenerative diseases.Use of Caenorhabditis elegans as a model to study Alzheimer's disease and other neurodegenerative diseases.Motor neuron disease-frontotemporal dementia: a clinical continuum.C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian population.Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies.

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P2860

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

http://www.wikidata.org/entity/Q35984663

description

2012 nî lūn-bûn

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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

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

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Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

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type

label

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

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Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

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prefLabel

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

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Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

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P356

J.NEUROBIOLAGING.2012.05.007

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Neurobiology of Aging

P1476

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

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P2093

Alan E Renton

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Bryan J Traynor

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Elisa Majounie

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Margaux F Keller

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Yevgeniya Abramzon

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P2860

A two-stage meta-analysis identifies several new loci for Parkinson's disease

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

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

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

Role of mendelian genes in "sporadic" Parkinson's disease.

Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

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

A systematic review of prevalence studies of dementia in Parkinson's disease.

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10.1016/J.NEUROBIOLAGING.2012.05.007

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Andrew Singleton

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Parkinson's disease

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