相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Large C9orf72 repeat expansions are seen in Chinese patients with sporadic amyotrophic lateral sclerosis
Yongping Chen et al.
NEUROBIOLOGY OF AGING (2016)
The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism
Lucia V. Schottlaender et al.
NEUROBIOLOGY OF AGING (2015)
Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansions
Sonja W. Scholz et al.
NEUROBIOLOGY OF AGING (2015)
Absence of C9ORF72 Expanded or Intermediate Repeats in Autopsy-Confirmed Parkinson's Disease
Karen Nuytemans et al.
MOVEMENT DISORDERS (2014)
Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases
Annemarie Huebers et al.
NEUROBIOLOGY OF AGING (2014)
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum
Nicola Ticozzi et al.
NEUROBIOLOGY OF AGING (2014)
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease
Jessie Theuns et al.
NEUROLOGY (2014)
Multiple System Atrophy and Amyotrophic Lateral Sclerosis in a Family With Hexanucleotide Repeat Expansions in C9orf72
Jill S. Goldman et al.
JAMA NEUROLOGY (2014)
Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders
Chin-Hsien Lin et al.
FRONTIERS IN NEUROLOGY (2014)
Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population
Jon Beck et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease
Karen Nuytemans et al.
ANNALS OF HUMAN GENETICS (2013)
C9orf72 repeat expansions are a rare genetic cause of parkinsonism
Suzanne Lesage et al.
BRAIN (2013)
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease
S. G. Lindquist et al.
CLINICAL GENETICS (2013)
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder
Bradley N. Smith et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Parkinson disease is not associated with C9ORF72 repeat expansions
Matthew B. Harms et al.
NEUROBIOLOGY OF AGING (2013)
Investigation of C9orf72 repeat expansions in Parkinson's disease
Hussein Daoud et al.
NEUROBIOLOGY OF AGING (2013)
C9ORF72 expansions, parkinsonism, and Parkinson disease A clinicopathologic study
Johnathan Cooper-Knock et al.
NEUROLOGY (2013)
Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome
Mariely DeJesus-Hernandez et al.
PARKINSONISM & RELATED DISORDERS (2013)
Current insights into the C9orf72 repeat expansion diseases of the FTLD/ALS spectrum
Marc Cruts et al.
TRENDS IN NEUROSCIENCES (2013)
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China
Bin Jiao et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2013)
Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion
Marco Luigetti et al.
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)
No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden
Chizuru Akimoto et al.
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)
Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort
Tim Van Langenhove et al.
JAMA NEUROLOGY (2013)
Characterization of a Family With c9FTD/ALS Associated With the GGGGCC Repeat Expansion in C9ORF72
Rodolfo Savica et al.
ARCHIVES OF NEUROLOGY (2012)
Frontotemporal Dementia in a Brazilian Kindred With the C9orf72 Mutation
Leonel T. Takada et al.
ARCHIVES OF NEUROLOGY (2012)
Investigation of C9orf72 in 4 Neurodegenerative Disorders
Zhengrui Xi et al.
ARCHIVES OF NEUROLOGY (2012)
Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p
Ging-Yuek R. Hsiung et al.
BRAIN (2012)
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie et al.
LANCET NEUROLOGY (2012)
Large C9orf72 repeat expansions are not a common cause of Parkinson's disease
Elisa Majounie et al.
NEUROBIOLOGY OF AGING (2012)
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