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Volumn 64, Issue 8, 2012, Pages 937-941

Spinocerebellar ataxia type 36 (nicknamed Asidan)

Author keywords

Asidan; Dementia; GGCCTG hexanucleotide expansion; NOP56; SCA36

Indexed keywords

CYTOSINE; GUANINE; NUCLEOLIN; THYMINE;

EID: 84865310495     PISSN: 18816096     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (4)

References (11)
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    • A case of spinocerebellar ataxia accompanied by severe involvement of the motor neuron system
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    • Manabe, Y.1    Shiro, Y.2    Takahashi, K.3    Kashihara, K.4    Abe, K.5
  • 2
    • 34250162883 scopus 로고    scopus 로고
    • Two cases of spinocerebellar ataxia accompanied by involvement of the skeletal motor neuron system and bulbar palsy
    • Ohta Y, Hayashi T, Nagai M, Okamoto M, Nagotani S, et al: Two cases of spinocerebellar ataxia accompanied by involvement of the skeletal motor neuron system and bulbar palsy. Intern Med 46: 751-755, 2007
    • (2007) Intern Med , vol.46 , pp. 751-755
    • Ohta, Y.1    Hayashi, T.2    Nagai, M.3    Okamoto, M.4    Nagotani, S.5
  • 3
    • 80051549115 scopus 로고    scopus 로고
    • Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement
    • Kobayashi H, Abe K, Matsuura T, Ikeda Y, Hitomi T, et al: Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement. Am J Hum Genet 89: 121-130, 2011
    • (2011) Am J Hum Genet , vol.89 , pp. 121-130
    • Kobayashi, H.1    Abe, K.2    Matsuura, T.3    Ikeda, Y.4    Hitomi, T.5
  • 5
    • 78649890408 scopus 로고    scopus 로고
    • TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing
    • Wang JL, Yang X, Xia K, Hu ZM, Weng L, et al: TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. Brain 133: 3510-3518, 2010
    • (2010) Brain , vol.133 , pp. 3510-3518
    • Wang, J.L.1    Yang, X.2    Xia, K.3    Hu, Z.M.4    Weng, L.5
  • 6
    • 0029969662 scopus 로고    scopus 로고
    • Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease
    • Watanabe M, Abe K, Aoki M, Kameya T, Kaneko J, et al: Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease. J Neurol Sci 136: 101-107, 1996
    • (1996) J Neurol Sci , vol.136 , pp. 101-107
    • Watanabe, M.1    Abe, K.2    Aoki, M.3    Kameya, T.4    Kaneko, J.5
  • 7
    • 0029049256 scopus 로고
    • Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan
    • Kameya T, Abe K, Aoki M, Sahara M, Tobita M, et al: Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan. Neurology 45: 1587-1594, 1995
    • (1995) Neurology , vol.45 , pp. 1587-1594
    • Kameya, T.1    Abe, K.2    Aoki, M.3    Sahara, M.4    Tobita, M.5
  • 8
    • 9244229051 scopus 로고    scopus 로고
    • Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1
    • Goldfarb LG, Vasconcelos O, Platonov FA, Lunkes A, Kipnis V, et al: Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1. Ann Neurol 39: 500-506, 1996
    • (1996) Ann Neurol , vol.39 , pp. 500-506
    • Goldfarb, L.G.1    Vasconcelos, O.2    Platonov, F.A.3    Lunkes, A.4    Kipnis, V.5
  • 9
    • 84865332523 scopus 로고    scopus 로고
    • Clinical features of SCA36: A novel hereditary dominant spinocerebellar ataxia with motor neuron involvement (Asidan)
    • in press
    • Ikeda Y, Ohta Y, Kobayashi H, Okamoto M, Takamatsu K, et al: Clinical features of SCA36: a novel hereditary dominant spinocerebellar ataxia with motor neuron involvement (Asidan). Neurology, 2012 (in press)
    • (2012) Neurology
    • Ikeda, Y.1    Ohta, Y.2    Kobayashi, H.3    Okamoto, M.4    Takamatsu, K.5
  • 10
    • 79955964913 scopus 로고    scopus 로고
    • Comparisons of acoustic function in SCA31 and other forms of ataxias
    • Ikeda Y, Nagai M, Kurata T, Yamashita T, Ohta Y, et al: Comparisons of acoustic function in SCA31 and other forms of ataxias. Neurol Res 33: 427-432, 2011
    • (2011) Neurol Res , vol.33 , pp. 427-432
    • Ikeda, Y.1    Nagai, M.2    Kurata, T.3    Yamashita, T.4    Ohta, Y.5
  • 11
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    • Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan
    • Feb 21 [Epub ahead of print]
    • Abe K, Ikeda Y, Kurata T, Ohta Y, Manabe Y, et al: Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan. Eur J Neurol, 2012 Feb 21 [Epub ahead of print]
    • (2012) Eur J Neurol
    • Abe, K.1    Ikeda, Y.2    Kurata, T.3    Ohta, Y.4    Manabe, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.