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Volumn 80, Issue 1, 2009, Pages 94-95

Late-onset tay-Sachs disease presenting as a childhood stutter

Author keywords

[No Author keywords available]

Indexed keywords

BETA N ACETYLHEXOSAMINIDASE A;

EID: 58249091635     PISSN: 00223050     EISSN: 1468330X     Source Type: Journal    
DOI: 10.1136/jnnp.2008.147645     Document Type: Letter
Times cited : (14)

References (5)
  • 1
    • 0029586331 scopus 로고
    • Tay-Sachs disease with atypical chronic course and limited brain storage: Alpha-locus Hexosaminidase genetic compound
    • Philippart M, Carrel RE, Landing BH. Tay-Sachs disease with atypical chronic course and limited brain storage: Alpha-locus Hexosaminidase genetic compound. Neurochem Res 1995: 20,11:1323-8.
    • (1995) Neurochem Res , vol.20 , Issue.11 , pp. 1323-1328
    • Philippart, M.1    Carrel, R.E.2    Landing, B.H.3
  • 2
    • 0033779147 scopus 로고    scopus 로고
    • Brain correlates of stuttering and syllable production. A PET performance-correlation and analysis
    • Fox FT, Ingham RJ, Ingham JC, et al. Brain correlates of stuttering and syllable production. A PET performance-correlation and analysis. Brain 2000; 123:1985-2004.
    • (2000) Brain , vol.123 , pp. 1985-2004
    • Fox, F.T.1    Ingham, R.J.2    Ingham, J.C.3
  • 3
    • 8644264058 scopus 로고    scopus 로고
    • Aberrant auditory processing and atypical planum temporale in developmental stuttering
    • Foundas AL, Bollich AM, Feldman J, et al. Aberrant auditory processing and atypical planum temporale in developmental stuttering. Neurology 2004; 63:1640-6.
    • (2004) Neurology , vol.63 , pp. 1640-1646
    • Foundas, A.L.1    Bollich, A.M.2    Feldman, J.3
  • 4
    • 33645461964 scopus 로고    scopus 로고
    • New complexities in the genetics of stuttering: Significant sex-specific linkage signals
    • Suresh R, Ambrose N, Roe C, et al. New complexities in the genetics of stuttering: significant sex-specific linkage signals. Am J Hum Genet 2006; 78:554-63.
    • (2006) Am J Hum Genet , vol.78 , pp. 554-563
    • Suresh, R.1    Ambrose, N.2    Roe, C.3
  • 5
    • 0028180764 scopus 로고
    • Mutations in the lysosomal β-galactosidase gene that causes the adult form of 6M1 gangliosidosis
    • Chakraborty S, Rati MA, Wenger DA. Mutations in the lysosomal β-galactosidase gene that causes the adult form of 6M1 gangliosidosis. Am J Hum Genet 1994; 54:1004-13.
    • (1994) Am J Hum Genet , vol.54 , pp. 1004-1013
    • Chakraborty, S.1    Rati, M.A.2    Wenger, D.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.