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Volumn 82, Issue 1, 2014, Pages 49-56

Neuroimaging and clinical features in type II (late-onset) Alexander disease

Author keywords

[No Author keywords available]

Indexed keywords

GLIAL FIBRILLARY ACIDIC PROTEIN;

EID: 84892148676     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000438230.33223.bc     Document Type: Article
Times cited : (66)

References (18)
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  • 2
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    • Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease
    • DOI 10.1038/83679
    • Brenner M, Johnson AB, Boespflug-Tanguy O, Rodriguez D, Goldman JE, Messing A. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet 2001;27:117-120. (Pubitemid 32044531)
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  • 6
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    • Neuro-ophthalmic, radiographic, and pathologic manifestations of adult- onset Alexander disease
    • Martidis A, Yee RD, Azzarelli B, Biller J. Neuro-ophthalmic, radiographic, and pathologic manifestations of adult-onset Alexander disease. Arch Ophthalmol 1999;117:265-267. (Pubitemid 29091829)
    • (1999) Archives of Ophthalmology , vol.117 , Issue.2 , pp. 265-267
    • Martidis, A.1    Yee, R.D.2    Azzarelli, B.3    Biller, J.4
  • 7
    • 77950528261 scopus 로고    scopus 로고
    • Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: A case report and review of the literature
    • Namekawa M, Takiyama Y, Honda J, Shimazaki H, Sakoe K, Nakano I. Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature. BMC Neurol 2010;10:21.
    • (2010) BMC Neurol , vol.10 , pp. 21
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  • 8
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    • Adult-onset Alexander disease: A series of eleven unrelated cases with review of the literature
    • Pareyson D, Fancellu R, Mariotti C, et al. Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature. Brain 2008;131:2321-2331.
    • (2008) Brain , vol.131 , pp. 2321-2331
    • Pareyson, D.1    Fancellu, R.2    Mariotti, C.3
  • 9
    • 0029445919 scopus 로고
    • Hereditary adult-onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxia
    • Schwankhaus JD, Parisi JE, Gulledge WR, Chin L, Currier RD. Hereditary adult-onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxia. Neurology 1995;45:2266-2271. (Pubitemid 27100260)
    • (1995) Neurology , vol.45 , Issue.12 , pp. 2266-2271
    • Schwankhaus, J.D.1    Parisi, J.E.2    Gulledge, W.R.3    Chin, L.4    Currier, R.D.5
  • 13
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    • GFAP mutations, age at onset, and clinical subtypes in Alexander disease
    • Prust M, Wang J, Morizono H, et al. GFAP mutations, age at onset, and clinical subtypes in Alexander disease. Neurology 2011;77:1287-1294.
    • (2011) Neurology , vol.77 , pp. 1287-1294
    • Prust, M.1    Wang, J.2    Morizono, H.3
  • 17
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    • The clinical spectrum of late-onset Alexander disease: A systematic literature review
    • Balbi P, Salvini S, Fundaro C, et al. The clinical spectrum of late-onset Alexander disease: a systematic literature review. J Neurol 2010;257:1955-1962.
    • (2010) J Neurol , vol.257 , pp. 1955-1962
    • Balbi, P.1    Salvini, S.2    Fundaro, C.3
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.