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Volumn 51, Issue 6, 2009, Pages 610-612

Dentatorubral pallidoluysian atrophy in a Turkish family

Author keywords

Autosomal dominant inheritance; Child; Myoclonic epilepsy; Progressive ataxia

Indexed keywords

ADENINE; ATROPINE; CYTOSINE; GUANOSINE;

EID: 76649104725     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (10)
  • 1
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    • 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
    • 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. Nature Genet 1994; 6: 9-13.
    • (1994) Nature Genet , vol.6 , pp. 9-13
    • Nagafuchi, S.1    Yanagisawa, H.2    Sato, K.3
  • 3
    • 0032618291 scopus 로고    scopus 로고
    • Dentatorubral-pallidoluysian atrophy: Clinical features and molecular genetics
    • Tsuji S. Dentatorubral-pallidoluysian atrophy: clinical features and molecular genetics. Adv Neurol 1999; 79: 399-409.
    • (1999) Adv Neurol , vol.79 , pp. 399-409
    • Tsuji, S.1
  • 4
    • 0036157660 scopus 로고    scopus 로고
    • Juvenile dentatorubral pallidoluysian atrophy: New clinical features
    • Licht DJ, Lynch DR. Juvenile dentatorubral pallidoluysian atrophy: new clinical features. Pediatr Neurol 2002; 26: 51-54.
    • (2002) Pediatr Neurol , vol.26 , pp. 51-54
    • Licht, D.J.1    Lynch, D.R.2
  • 5
    • 15044357259 scopus 로고    scopus 로고
    • Progressive myoclonic epilepsies: A review of genetic and therapeutic aspects
    • Shafwan A, Farrell M, Delanty N. Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects. Lancet Neurol 2005; 4: 239-248.
    • (2005) Lancet Neurol , vol.4 , pp. 239-248
    • Shafwan, A.1    Farrell, M.2    Delanty, N.3
  • 6
    • 0035936637 scopus 로고    scopus 로고
    • Severe infantile dentatorubral pallidoluysian atrophy with extreme expansion of CAG repeats
    • Shimojo Y, Osawa Y, Fukumizu M, et al. Severe infantile dentatorubral pallidoluysian atrophy with extreme expansion of CAG repeats. Neurology 2001; 56: 277-278.
    • (2001) Neurology , vol.56 , pp. 277-278
    • Shimojo, Y.1    Osawa, Y.2    Fukumizu, M.3
  • 7
    • 0028060244 scopus 로고
    • Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)
    • Nagafuchi S, Yanagisawa H, Ohsaki E, et al. Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA). Nat Genet 1994; 8: 177-182.
    • (1994) Nat Genet , vol.8 , pp. 177-182
    • Nagafuchi, S.1    Yanagisawa, H.2    Ohsaki, E.3
  • 8
    • 0029865956 scopus 로고    scopus 로고
    • Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: The mutant allele is preferentially transmitted in male meiosis
    • Ikeuchi T, Igarashi S, Takiyama Y, et al. Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis. Am J Hum Genet 1996; 58: 730-733.
    • (1996) Am J Hum Genet , vol.58 , pp. 730-733
    • Ikeuchi, T.1    Igarashi, S.2    Takiyama, Y.3
  • 9
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.