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Volumn 15, Issue 4, 2008, Pages 154-155

An Instructive Case of an 8-Year-Old Boy With Intellectual Disability

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN;

EID: 57349084143     PISSN: 10719091     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.spen.2008.09.002     Document Type: Article
Times cited : (11)

References (9)
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    • Shevell, M.I.1    Bejjani, B.A.2    Srour, M.3
  • 2
    • 0028027687 scopus 로고
    • Becker muscular dystrophy with onset after 60 years
    • Heald A., Anderson L.V., Bushby K.M., et al. Becker muscular dystrophy with onset after 60 years. Neurology 44 (1994) 2388-2390
    • (1994) Neurology , vol.44 , pp. 2388-2390
    • Heald, A.1    Anderson, L.V.2    Bushby, K.M.3
  • 3
    • 0028341862 scopus 로고
    • Severe mental retardation in a young boy with an in-frame deletion in the dystrophin gene
    • Colomer J., Gallano P., Nicholson L.V., et al. Severe mental retardation in a young boy with an in-frame deletion in the dystrophin gene. Eur J Pediatr 153 (1994) 492-494
    • (1994) Eur J Pediatr , vol.153 , pp. 492-494
    • Colomer, J.1    Gallano, P.2    Nicholson, L.V.3
  • 4
    • 0032731729 scopus 로고    scopus 로고
    • Confirmation of Angelman syndrome in a boy previously reported as having Becker muscular dystrophy and severe mental retardation
    • Poyatos D., Coll M.D., Guitart M., et al. Confirmation of Angelman syndrome in a boy previously reported as having Becker muscular dystrophy and severe mental retardation. Eur J Pediatr 158 (1999) 1006
    • (1999) Eur J Pediatr , vol.158 , pp. 1006
    • Poyatos, D.1    Coll, M.D.2    Guitart, M.3
  • 5
    • 0034068415 scopus 로고    scopus 로고
    • Brain dystrophin, neurogenetics and mental retardation
    • Mehler M.F. Brain dystrophin, neurogenetics and mental retardation. Brain Res Rev 32 (2000) 277-307
    • (2000) Brain Res Rev , vol.32 , pp. 277-307
    • Mehler, M.F.1
  • 6
    • 33746125276 scopus 로고    scopus 로고
    • Different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy
    • Lo I.F., Lai K.K., Tong T.M., et al. Different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy. Chin Med J (Engl) 119 (2006) 1079-1087
    • (2006) Chin Med J (Engl) , vol.119 , pp. 1079-1087
    • Lo, I.F.1    Lai, K.K.2    Tong, T.M.3
  • 7
    • 0842310824 scopus 로고    scopus 로고
    • Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy
    • Giliberto F., Ferreiro V., Dalamon V., et al. Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy. Neurol Res 26 (2004) 83-87
    • (2004) Neurol Res , vol.26 , pp. 83-87
    • Giliberto, F.1    Ferreiro, V.2    Dalamon, V.3
  • 8
    • 0034163482 scopus 로고    scopus 로고
    • Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies
    • Bardoni A., Felisari G., Sironi M., et al. Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies. Neuromuscul Disor 10 (2000) 194-199
    • (2000) Neuromuscul Disor , vol.10 , pp. 194-199
    • Bardoni, A.1    Felisari, G.2    Sironi, M.3
  • 9
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    • Practice parameter: Corticosteroid treatment of Duchenne dystrophy
    • Moxley III R.T., Ashwal S., Pandya S., et al. Practice parameter: Corticosteroid treatment of Duchenne dystrophy. Neurol 64 (2005) 13-20
    • (2005) Neurol , vol.64 , pp. 13-20
    • Moxley III, R.T.1    Ashwal, S.2    Pandya, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.