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Volumn 8, Issue 5, 2012, Pages 249-250

Motor neuron disease: The C9orf72 hexanucleotide repeat expansion in FTD and ALS

Author keywords

[No Author keywords available]

Indexed keywords

TAR DNA BINDING PROTEIN;

EID: 84860883638     PISSN: 17594758     EISSN: 17594766     Source Type: Journal    
DOI: 10.1038/nrneurol.2012.58     Document Type: Review
Times cited : (13)

References (9)
  • 1
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    • Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
    • De Jesus-Hernandez, M. et al. Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72, 245-256 (2011).
    • (2011) Neuron , vol.72 , pp. 245-256
    • De Jesus-Hernandez, M.1
  • 2
    • 80054837386 scopus 로고    scopus 로고
    • A nexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
    • Renton, A. E. et al. A nexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 71, 257-268 (2011).
    • (2011) Neuron , vol.71 , pp. 257-268
    • Renton, A.E.1
  • 3
    • 84857516402 scopus 로고    scopus 로고
    • The clinical and pathological phenotype of C9orf72 hexanucleotide repeat expansions
    • Simon-Sanchez, J. et al. The clinical and pathological phenotype of C9orf72 hexanucleotide repeat expansions. Brain http://dx.doi.org/10.1093/brain/ awr353.
    • Brain
    • Simon-Sanchez, J.1
  • 4
    • 84863393065 scopus 로고    scopus 로고
    • Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
    • Snowden, J. S. et al. Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations. Brain http://dx.doi.org/10.1093/brain/awr355.
    • Brain
    • Snowden, J.S.1
  • 5
    • 33749668518 scopus 로고    scopus 로고
    • Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: Classification and relation to clinical phenotype
    • Mackenzie, I. R. et al. Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype. Acta Neuropathol. 112, 539-549 (2006).
    • (2006) Acta Neuropathol. , vol.112 , pp. 539-549
    • MacKenzie, I.R.1
  • 6
    • 79959599081 scopus 로고    scopus 로고
    • A harmonized classification system for FTLD-TDP pathology
    • Mackenzie, I. R. et al. A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol. 122, 111-113 (2011).
    • (2011) Acta Neuropathol. , vol.122 , pp. 111-113
    • MacKenzie, I.R.1
  • 7
    • 84857050135 scopus 로고    scopus 로고
    • Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: A population-based cohort study
    • Byrne, S. et al. Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study. Lancet Neurol. 11, 232-240 (2012).
    • (2012) Lancet Neurol. , vol.11 , pp. 232-240
    • Byrne, S.1
  • 8
    • 82355180849 scopus 로고    scopus 로고
    • Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
    • Murray, M. E. et al. Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72. Acta Neuropathol. 122, 673-690 (2011).
    • (2011) Acta Neuropathol. , vol.122 , pp. 673-690
    • Murray, M.E.1
  • 9
    • 84857921617 scopus 로고    scopus 로고
    • Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene of chromosome 9p
    • Stewart, H. et al. Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene of chromosome 9p. Acta Neuropathol. 123, 409-417 (2012).
    • (2012) Acta Neuropathol. , vol.123 , pp. 409-417
    • Stewart, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.