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Volumn 11, Issue 6, 1996, Pages 439-444

Leukoencephalopathy, megalencephaly, and mild clinical course. A recently individualized familial leukodystrophy. Report on five new cases

Author keywords

[No Author keywords available]

Indexed keywords

ALEXANDER DISEASE; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DISEASE COURSE; EPILEPSY; FAMILIAL DISEASE; FRONTAL LOBE; HUMAN; INFANT; LEUKODYSTROPHY; LEUKOENCEPHALOPATHY; MALE; PRIORITY JOURNAL; TEMPORAL LOBE;

EID: 0029823879     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307389601100604     Document Type: Article
Times cited : (68)

References (10)
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  • 2
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  • 3
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    • Leukoencephalopathy with swelling and a discrepantly mild clinical course in eight children
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    • Van Der Knaap, M.S.1    Barth, P.G.2    Stroink, H.3
  • 4
    • 0023818297 scopus 로고
    • Aspartaoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease
    • Matalon R, Michals K, Sebesta D, et al: Aspartaoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease. Am J Med Genet 1988;29:463-471.
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  • 7
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    • L-2-Hydroxyglutaric acidemia: A novel inherited neurometabolic disease
    • Barth PG, Hoffmann GF, Jaeken J, et al: L-2-Hydroxyglutaric acidemia: A novel inherited neurometabolic disease. Ann Neurol 1992;32:66-71.
    • (1992) Ann Neurol , vol.32 , pp. 66-71
    • Barth, P.G.1    Hoffmann, G.F.2    Jaeken, J.3
  • 9
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    • Congenital muscular dystrophy with cerebral white matter spongiosis
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  • 10
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    • Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblings
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.