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Volumn 21, Issue 1, 2000, Pages 224-227

Leigh syndrome in a 3-year-old boy with unusual brain MR imaging and pathologic findings

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; ELECTROENCEPHALOGRAM; ELECTRON MICROSCOPY; ENZYME DEFICIENCY; HUMAN; HUMAN TISSUE; LEIGH DISEASE; MALE; MENTAL DETERIORATION; MOTOR DYSFUNCTION; MUSCLE BIOPSY; NERVE DEGENERATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD;

EID: 0034000760     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (28)

References (12)
  • 1
    • 0023429777 scopus 로고
    • Cytochrome c oxidase deficiency in Leigh syndrome
    • DiMaurio S, Servidei S, Zeivani M, et al. Cytochrome c oxidase deficiency in Leigh syndrome. Ann Neurol 1987;22:498-506
    • (1987) Ann Neurol , vol.22 , pp. 498-506
    • Dimaurio, S.1    Servidei, S.2    Zeivani, M.3
  • 2
    • 0029877629 scopus 로고    scopus 로고
    • Clinical heterogenity associated with the mitochondrial DNA T8993C mutation
    • Santorelli FM, Mak SC, Vazquez-Memije ME, et al. Clinical heterogenity associated with the mitochondrial DNA T8993C mutation. Pediatr Res 1996;39:914-917
    • (1996) Pediatr Res , vol.39 , pp. 914-917
    • Santorelli, F.M.1    Mak, S.C.2    Vazquez-Memije, M.E.3
  • 3
    • 0025228482 scopus 로고
    • MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh disease): Correlation with biochemical defect
    • Medina L, Chi TL, DeVivo DC, Hilal SK. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh disease): correlation with biochemical defect. AJNR Am J Neuroradiol 1990;11:379-384
    • (1990) AJNR Am J Neuroradiol , vol.11 , pp. 379-384
    • Medina, L.1    Chi, T.L.2    DeVivo, D.C.3    Hilal, S.K.4
  • 4
    • 0028926759 scopus 로고
    • Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome
    • Zafeiriou DI, Koletzko B, Mueller-Felber W, Paetzke I, Kueffer G, Jensen M. Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome. Brain Dev 1995;17:117-121
    • (1995) Brain Dev , vol.17 , pp. 117-121
    • Zafeiriou, D.I.1    Koletzko, B.2    Mueller-Felber, W.3    Paetzke, I.4    Kueffer, G.5    Jensen, M.6
  • 6
    • 0000376151 scopus 로고
    • Subacute necrotizing encephalomyelopathy in an infant
    • Leigh D. Subacute necrotizing encephalomyelopathy in an infant. J Neurol Neurosurg Psychiatry 1951;14:216-221
    • (1951) J Neurol Neurosurg Psychiatry , vol.14 , pp. 216-221
    • Leigh, D.1
  • 7
    • 0342709131 scopus 로고
    • Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency
    • Willems JL, Monnens LAH, Trijbels JMF, et al. Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency. J Inher Metab Dis 1983;6:121-122
    • (1983) J Inher Metab Dis , vol.6 , pp. 121-122
    • Willems, J.L.1    Monnens, L.A.H.2    Trijbels, J.M.F.3
  • 8
    • 0022497643 scopus 로고
    • Magnetic resonance imaging in subacute necrotizing encephalomyelopathy (Leigh disease)
    • Koch TK Yee MHC, Hutchinson HT, Berg BO. Magnetic resonance imaging in subacute necrotizing encephalomyelopathy (Leigh disease). Ann Neurol 1986;19:605-607
    • (1986) Ann Neurol , vol.19 , pp. 605-607
    • Koch, T.K.1    Yee, M.H.C.2    Hutchinson, H.T.3    Berg, B.O.4
  • 11
    • 0027228506 scopus 로고
    • Mitochondrial disorders: Analysis of their clinical and imaging characteristics
    • Barkovich AJ, Good WV, Koch TK, Berg BO. Mitochondrial disorders: analysis of their clinical and imaging characteristics. AJNR Am J Neuroradiol 1993;14:1119-1137
    • (1993) AJNR Am J Neuroradiol , vol.14 , pp. 1119-1137
    • Barkovich, A.J.1    Good, W.V.2    Koch, T.K.3    Berg, B.O.4
  • 12
    • 0031782160 scopus 로고    scopus 로고
    • Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiency
    • Harpey JP, Heron D, Prudent M, et al. Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiency. J Inher Metab Dis 1998;21:748-752
    • (1998) J Inher Metab Dis , vol.21 , pp. 748-752
    • Harpey, J.P.1    Heron, D.2    Prudent, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.