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Neurology
Volumn 47, Issue 6, 1996, Pages 1578-1580
Diagnosis of patients presenting to a huntington disease (HD) clinic without a family history of HD
Author keywords

[No Author keywords available]
Indexed keywords

ADULT; ALLELE; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; FAMILY HISTORY; GENETIC SUSCEPTIBILITY; HUMAN; HUNTINGTON CHOREA; MENTAL STRESS; MOTOR DYSFUNCTION; PRIORITY JOURNAL;
EID: 0029752786     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.47.6.1578     Document Type: Article
Times cited : (11)
References (10)
  • 1
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993;72: 971-983.
    • (1993) Cell , vol.72 , pp. 971-983
  • 3
    • 0028107864 scopus 로고
    • Mutation analysis in patients with possible but apparently sporadic Huntington's disease
    • Davis MB, Bateman D, Quinn NP, Marsden CD, Harding AE. Mutation analysis in patients with possible but apparently sporadic Huntington's disease. Lancet 1994;344:714-717.
    • (1994) Lancet , vol.344 , pp. 714-717
    • Davis, M.B.1    Bateman, D.2    Quinn, N.P.3    Marsden, C.D.4    Harding, A.E.5
  • 4
    • 0028985055 scopus 로고
    • Diagnosis of "sporadic" Huntington's disease
    • Dürr A, Dodé C, Hahn V, et al. Diagnosis of "sporadic" Huntington's disease. J Neurol Sci 1995;129:51-55.
    • (1995) J Neurol Sci , vol.129 , pp. 51-55
    • Dürr, A.1    Dodé, C.2    Hahn, V.3
  • 6
    • 0027176364 scopus 로고
    • The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
    • Andrew SE, Goldberg YP, Kremer B, et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nature Genet 1993;4:398-403.
    • (1993) Nature Genet , vol.4 , pp. 398-403
    • Andrew, S.E.1    Goldberg, Y.P.2    Kremer, B.3
  • 7
    • 0027261537 scopus 로고
    • Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
    • Snell RG, MacMillan JC, Cheadle JP, et al. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nature Genet 1993;4:393-397.
    • (1993) Nature Genet , vol.4 , pp. 393-397
    • Snell, R.G.1    MacMillan, J.C.2    Cheadle, J.P.3
  • 8
    • 0027443824 scopus 로고
    • Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign chorea
    • MacMillan JC, Morrison PJ, Nevin NC, et al. Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign chorea. J Med Genet 1993;30:1012-1013.
    • (1993) J Med Genet , vol.30 , pp. 1012-1013
    • MacMillan, J.C.1    Morrison, P.J.2    Nevin, N.C.3
  • 9
    • 0028110333 scopus 로고
    • Normal CAG repeat length in the Huntington's disease gene in senile chorea
    • Shinotoh H, Calne DB, Snow B, et al. Normal CAG repeat length in the Huntington's disease gene in senile chorea. Neurology 1994;44:2183-2184.
    • (1994) Neurology , vol.44 , pp. 2183-2184
    • Shinotoh, H.1    Calne, D.B.2    Snow, B.3
  • 10
    • 0028999064 scopus 로고
    • Hereditary late-onset chorea without significant dementia: Genetic evidence for substantial phenotypic variation in Huntington's disease
    • Britton JW, Uitti RJ, Ahlskog JE, Robinson RG, Kremer B, Hayden MR. Hereditary late-onset chorea without significant dementia: genetic evidence for substantial phenotypic variation in Huntington's disease. Neurology 1995;45:443-447.
    • (1995) Neurology , vol.45 , pp. 443-447
    • Britton, J.W.1    Uitti, R.J.2    Ahlskog, J.E.3    Robinson, R.G.4    Kremer, B.5    Hayden, M.R.6

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.