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Volumn 13, Issue 4, 2000, Pages 451-455

Recent advances in degenerative ataxias

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIA; FRIEDREICH ATAXIA; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; NEUROPATHOLOGY; REVIEW; SPINOCEREBELLAR DEGENERATION; TRINUCLEOTIDE REPEAT;

EID: 0033864505     PISSN: 13507540     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019052-200008000-00014     Document Type: Review
Times cited : (31)

References (44)
  • 1
    • 0020641096 scopus 로고
    • Classification of the hereditary ataxias and paraplegias
    • (1983) Lancet , vol.1 , pp. 1151-1155
    • Harding, A.E.1
  • 9
    • 0033054177 scopus 로고    scopus 로고
    • The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis
    • (1999) Hum Mol Genet , vol.8 , pp. 425-430
    • Wong, A.1    Yang, J.2    Cavadini, P.3
  • 22
    • 0032769095 scopus 로고    scopus 로고
    • Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6
    • (1999) Hum Mol Genet , vol.8 , pp. 1185-1193
    • Ishikawa, K.1    Fujigasaki, H.2    Saegusa, H.3
  • 33
    • 0033391428 scopus 로고    scopus 로고
    • Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice
    • (1999) Neuron , vol.24 , pp. 879-892
    • Cummings, C.J.1    Reinstein, E.2    Sun, Y.L.3
  • 39
    • 0032842276 scopus 로고    scopus 로고
    • Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxia
    • (1999) J Neurol , vol.246 , pp. 716-719
    • Hassin, B.S.1    Bar, S.A.2    Gilad, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.