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Volumn 27, Issue 3, 2002, Pages 217-220

Infantile spongiform leukoencephalopathy: Clinical and neuropathologic findings

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ASTROCYTE; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; ELECTRON MICROSCOPY; FEEDING DISORDER; GENETIC DISORDER; GLIOSIS; HEAD CIRCUMFERENCE; HUMAN; HUMAN TISSUE; HYPERPLASIA; INFANT; LEUKOENCEPHALOPATHY; MALE; MYELINATION; NERVE DEGENERATION; NEUROPATHOLOGY; NYSTAGMUS; PRIORITY JOURNAL; RADIODIAGNOSIS; SPASTICITY; WHITE MATTER;

EID: 0036711494     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(02)00427-7     Document Type: Article
Times cited : (3)

References (14)
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  • 5
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    • Histopathology of an infantile-onset spongiform leukoencephalopathy with a discrepantly mild clinical course
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  • 10
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  • 12
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    • Subunits of translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter
    • Leegwater P.A., Vermeulen G., Konst A.A.M., et al. Subunits of translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter. Nat Genet. 29:2001;383-388.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.