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Volumn 50, Issue 1, 1998, Pages 282-283

Sporadic cases of dentatorubral-pallidoluysian atrophy associated with maternal transmission

Author keywords

[No Author keywords available]

Indexed keywords

TRINUCLEOTIDE;

EID: 0031882739     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.50.1.282     Document Type: Article
Times cited : (5)

References (10)
  • 1
    • 0020064620 scopus 로고
    • Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy
    • Naito H, Oyanagi S. Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy. Neurology 1982;32:798-807.
    • (1982) Neurology , vol.32 , pp. 798-807
    • Naito, H.1    Oyanagi, S.2
  • 2
    • 0028216760 scopus 로고
    • Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
    • Koide R, Ikeuchi T, Onodera O, et al. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nat Genet 1994;6:9-13.
    • (1994) Nat Genet , vol.6 , pp. 9-13
    • Koide, R.1    Ikeuchi, T.2    Onodera, O.3
  • 3
    • 0028335386 scopus 로고
    • Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
    • Nagafuchi S, Yanagisawa H, Sato K, et al. Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nat Genet 1994;6:14-18.
    • (1994) Nat Genet , vol.6 , pp. 14-18
    • Nagafuchi, S.1    Yanagisawa, H.2    Sato, K.3
  • 5
    • 0345561901 scopus 로고
    • Hereditary DRPLA family with markedly increased number of CAG repeats in maternal transmission
    • Tokyo
    • Nakamura K, Iwahashi K, Suwaki H, Nishimura K, Hayahara T. Hereditary DRPLA family with markedly increased number of CAG repeats in maternal transmission. Neurol Med (Tokyo) 1995;43:339-342.
    • (1995) Neurol Med , vol.43 , pp. 339-342
    • Nakamura, K.1    Iwahashi, K.2    Suwaki, H.3    Nishimura, K.4    Hayahara, T.5
  • 7
    • 0029044667 scopus 로고
    • Dentatorubral-pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat
    • Ikeuchi T, Koide R, Tanaka H, et al. Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat. Ann Neurol 1995;37:769-775.
    • (1995) Ann Neurol , vol.37 , pp. 769-775
    • Ikeuchi, T.1    Koide, R.2    Tanaka, H.3
  • 8
    • 0028815025 scopus 로고
    • DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: Correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation
    • Komure O, Sano A, Nishino N, et al. DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation. Neurology 1995;45:143-149.
    • (1995) Neurology , vol.45 , pp. 143-149
    • Komure, O.1    Sano, A.2    Nishino, N.3
  • 9
    • 0030015722 scopus 로고    scopus 로고
    • A sporadic case of dentatorubral pallidoluysian atrophy (DRPLA) with CAG repeat expansion but no clinical abnormalities in the father
    • Shimizu N, Yamami T, Nakayama M, Ikeuchi T, Koide R, Tsuji S. A sporadic case of dentatorubral pallidoluysian atrophy (DRPLA) with CAG repeat expansion but no clinical abnormalities in the father (letter). J Neurol Neurosurg Psychiatry 1996;61:113-114.
    • (1996) J Neurol Neurosurg Psychiatry , vol.61 , pp. 113-114
    • Shimizu, N.1    Yamami, T.2    Nakayama, M.3    Ikeuchi, T.4    Koide, R.5    Tsuji, S.6
  • 10
    • 25544473390 scopus 로고
    • Sporadic Huntington's disease due to maternal transmission
    • Sánchez A, Rosich M, Castellví-Bel S, et al. Sporadic Huntington's disease due to maternal transmission. Am J Hum Genet 1995;57(suppl):A227.
    • (1995) Am J Hum Genet , vol.57 , Issue.SUPPL.
    • Sánchez, A.1    Rosich, M.2    Castellví-Bel, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.