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Volumn 38, Issue 5, 1988, Pages 751-754

MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BRAIN DISEASE; CASE REPORT; EPILEPSY; FEMALE; GENETICS; HEREDITY; HISTOLOGY; HUMAN; LACTIC ACIDOSIS; MALE; MIGRAINE; MITOCHONDRION; MYOPATHY; PRIORITY JOURNAL; ULTRASTRUCTURE;

EID: 0023889006     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (167)

References (13)
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    • Dvorkin GS, Andermann F, Carpenter S, et al. Classical migraine, intractable epilepsy and multiple strokes: a syndrome related to mitochondrial encephalopathy. In: Andermann F, Lugaresi E, eds. Migraine and epilepsy. Boston: Butterworths, 1987:203–232.
    • (1987) Migraine and epilepsy , pp. 203-232
    • Dvorkin, G.S.1    Andermann, F.2    Carpenter, S.3
  • 3
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    • Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: A distinctive clinical syndrome
    • Pavlakis SG, Phillips PC, Di Mauro S, De Vivo DC, Rowland LP. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a distinctive clinical syndrome. Ann Neurol 1984;16:481–488.
    • (1984) Ann Neurol , vol.16 , pp. 481-488
    • Pavlakis, S.G.1    Phillips, P.C.2    Di Mauro, S.3    De Vivo, D.C.4    Rowland, L.P.5
  • 4
    • 0018071854 scopus 로고
    • Reincarnation in cultured muscle of mitochondrial abnormalities: Two patients with epilepsy and lactic acidosis
    • Askanas V, Engel WK, Britton DE, Adornato BT, Eiben RM. Reincarnation in cultured muscle of mitochondrial abnormalities: two patients with epilepsy and lactic acidosis. Arch Neurol 1978;35:801–809.
    • (1978) Arch Neurol , vol.35 , pp. 801-809
    • Askanas, V.1    Engel, W.K.2    Britton, D.E.3    Adornato, B.T.4    Eiben, R.M.5
  • 6
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    • Reversible alexia, mitochondrial myopathy, and lactic acidemia
    • Skoglund RR. Reversible alexia, mitochondrial myopathy, and lactic acidemia. Neurology 1979;29:717–720.
    • (1979) Neurology , vol.29 , pp. 717-720
    • Skoglund, R.R.1
  • 7
    • 0013506039 scopus 로고
    • The treatment of mitochondrial disease. Abstract
    • Peterson P, Martens M, Lee CP. The treatment of mitochondrial disease. Abstract. Neurology 1986;36(suppl 1):95.
    • (1986) Neurology , vol.36 , pp. 95
    • Peterson, P.1    Martens, M.2    Lee, C.P.3
  • 9
    • 0021175401 scopus 로고
    • Mitochondrial encephalomyopathy: Fluctuating symptoms and CT
    • Yamamoto T, Beppu H, Tsubaki T. Mitochondrial encephalomyopathy: fluctuating symptoms and CT. Neurology 1984;34:1456–1460.
    • (1984) Neurology , vol.34 , pp. 1456-1460
    • Yamamoto, T.1    Beppu, H.2    Tsubaki, T.3
  • 11
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    • Mitochondrial myopathies
    • Serratrice G, Cros D, Desnuelle C, et al, eds., New York: Raven Press
    • Morgan-Hughes JA, Hayes DJ, Clark JB. Mitochondrial myopathies. In: Serratrice G, Cros D, Desnuelle C, et al, eds. Neuromuscular diseases. New York: Raven Press, 1984:79–85.
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    • Morgan-Hughes, J.A.1    Hayes, D.J.2    Clark, J.B.3
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    • Cytochrome c oxydase deficiency: A remarkable spectrum of clinical and neuropathologic findings in a single family. Abstract
    • Berkovic SF, Carpenter S, Karpati G, Andermann F, Andermann E, Shoubridge E, Arnold D. Cytochrome c oxydase deficiency: a remarkable spectrum of clinical and neuropathologic findings in a single family. Abstract. Neurology 1987;37(suppl 1):223.
    • (1987) Neurology , vol.37 , pp. 223
    • Berkovic, S.F.1    Carpenter, S.2    Karpati, G.3    Andermann, F.4    Andermann, E.5    Shoubridge, E.6    Arnold, D.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.