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Volumn 22, Issue 1, 2001, Pages 55-56

Presymptomatic tests in Huntington's disease and dominant ataxias

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; FEMALE; GENETIC COUNSELING; GENETIC SCREENING; GENETICS; HUMAN; HUNTINGTON CHOREA; MALE; NEUROPSYCHOLOGICAL TEST; NUCLEOTIDE SEQUENCE; ONSET AGE; PATIENT EDUCATION; PREDICTION AND FORECASTING; PSYCHOLOGICAL ASPECT; SPINOCEREBELLAR DEGENERATION; STANDARD; TRINUCLEOTIDE REPEAT;

EID: 0035258138     PISSN: 15901874     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100720170044     Document Type: Article
Times cited : (18)

References (10)
  • 2
    • 0028023974 scopus 로고
    • Proceed with care: Direct predictive testing for Huntington disease
    • Benjamin CM, Adam S, Wiggins S et al (1994) Proceed with care: direct predictive testing for Huntington disease. Am J Hum Genet 55:606-617
    • (1994) Am J Hum Genet , vol.55 , pp. 606-617
    • Benjamin, C.M.1    Adam, S.2    Wiggins, S.3
  • 4
    • 0033358526 scopus 로고    scopus 로고
    • A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease
    • Almqvist E, Bloch M, Brinkman R et al (1999) A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease. Am J Hum Genet 64:1293-1304
    • (1999) Am J Hum Genet , vol.64 , pp. 1293-1304
    • Almqvist, E.1    Bloch, M.2    Brinkman, R.3
  • 5
    • 0027275819 scopus 로고
    • A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosome
    • Warner JP, Barron LH, Brock DJH (1993) A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosome. Mol Cell Probes 7:235-239
    • (1993) Mol Cell Probes , vol.7 , pp. 235-239
    • Warner, J.P.1    Barron, L.H.2    Brock, D.J.H.3
  • 6
    • 0028564730 scopus 로고
    • DNA haplo-type analysis of Huntington's disease reveals clues to the origins and mechanisms of CAG expansion and reason for geographic variations of prevalence
    • Squitieri F, Andrew SE, Goldgerg YP et al (1994) DNA haplo-type analysis of Huntington's disease reveals clues to the origins and mechanisms of CAG expansion and reason for geographic variations of prevalence. Hum Mol Genet 3:2103-2114
    • (1994) Hum Mol Genet , vol.3 , pp. 2103-2114
    • Squitieri, F.1    Andrew, S.E.2    Goldgerg, Y.P.3
  • 7
    • 0030155708 scopus 로고    scopus 로고
    • Update on genetics of Huntington's disease: Availability of direct and accurate predictive test
    • Squitieri F, Campanella G, Hayden MR (1996) Update on genetics of Huntington's disease: availability of direct and accurate predictive test. Ital J Neurol Sci 17:185-187
    • (1996) Ital J Neurol Sci , vol.17 , pp. 185-187
    • Squitieri, F.1    Campanella, G.2    Hayden, M.R.3
  • 8
    • 0033941655 scopus 로고    scopus 로고
    • Atypical movement disorders in the early stages of Huntington's disease: Clinical and genetic analysis
    • Squitieri F, Berardelli A, Nargi E et al (2000) Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis. Clin Genet 58:50-56
    • (2000) Clin Genet , vol.58 , pp. 50-56
    • Squitieri, F.1    Berardelli, A.2    Nargi, E.3
  • 9
    • 0033668365 scopus 로고    scopus 로고
    • Familial aggregation of psychotic symptoms in Huntington's disease
    • Tsuang D, Almqvist EW, Lipe H et al (2000) Familial aggregation of psychotic symptoms in Huntington's disease. Am J Psychiatry 157(12):1955-1959
    • (2000) Am J Psychiatry , vol.157 , Issue.12 , pp. 1955-1959
    • Tsuang, D.1    Almqvist, E.W.2    Lipe, H.3
  • 10
    • 0042115272 scopus 로고
    • Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: Evidence from single sperm analyses
    • Chong SS, Almqvist E, Telenius H et al (1995) Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses. Hum Mol Genet 2:301-309
    • (1995) Hum Mol Genet , vol.2 , pp. 301-309
    • Chong, S.S.1    Almqvist, E.2    Telenius, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.