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197 related items for PubMed ID: 3103091

  • 1. Pyruvate dehydrogenase complex deficiency as a cause of subacute necrotizing encephalopathy (Leigh disease).
    Kretzschmar HA, DeArmond SJ, Koch TK, Patel MS, Newth CJ, Schmidt KA, Packman S.
    Pediatrics; 1987 Mar; 79(3):370-3. PubMed ID: 3103091
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  • 2. [Leigh's subacute necrotizing encephalomyelopathy due to decreased activity of the pyruvate dehydrogenase complex].
    Siemes H, Goebel HH, Sengers RC, Ruitenbeek W, Trijbels JM.
    Monatsschr Kinderheilkd; 1987 Dec; 135(12):821-6. PubMed ID: 3125426
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  • 3. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.
    Medina L, Chi TL, DeVivo DC, Hilal SK.
    AJR Am J Roentgenol; 1990 Jun; 154(6):1269-74. PubMed ID: 2159689
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  • 4. Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy.
    Federico A, Dotti MT, Fabrizi GM, Palmeri S, Massimo L, Robinson BH, Malandrini A, Guazzi GC.
    Eur Neurol; 1990 Jun; 30(3):123-7. PubMed ID: 2162773
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  • 9. Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease).
    DeVivo DC, Haymond MW, Obert KA, Nelson JS, Pagliara AS.
    Ann Neurol; 1979 Dec; 6(6):483-94. PubMed ID: 119480
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  • 15. Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE).
    Kustermann-Kuhn B, Harzer K, Schröder R, Permanetter W, Peiffer J.
    Hum Genet; 1984 Dec; 68(1):51-3. PubMed ID: 6437963
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  • 17. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.
    Medina L, Chi TL, DeVivo DC, Hilal SK.
    AJNR Am J Neuroradiol; 1990 Dec; 11(2):379-84. PubMed ID: 2156413
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  • 18. Spectrum of neurological and survival outcomes in pyruvate dehydrogenase complex (PDC) deficiency: lack of correlation with genotype.
    DeBrosse SD, Okajima K, Zhang S, Nakouzi G, Schmotzer CL, Lusk-Kopp M, Frohnapfel MB, Grahame G, Kerr DS.
    Mol Genet Metab; 2012 Nov; 107(3):394-402. PubMed ID: 23021068
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