Works by Papadopoulou, Lefkothea C.


Results: 7
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    Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.

    Published in:
    Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513
    By:
    • Papadopoulou, Lefkothea C.;
    • Sue, Carolyn M.;
    • Davidson, Mercy M.;
    • Tanji, Kurenai;
    • Nishino, Ichizo;
    • Sadlock, James E.;
    • Krishna, Sindu;
    • Walker, Winsome;
    • Selby, Jeanette;
    • Glerum, D. Moira;
    • Coster, Rudy Van;
    • Lyon, Gilles;
    • Scalais, Emmanuel;
    • Lebel, Roger;
    • Kaplan, Paige;
    • Shanske, Sara;
    • De Vivo, Darryl C.;
    • Bonilla, Eduardo;
    • Hirano, Michio
    Publication type:
    Article
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    Protein Transduction Domain-Mediated Delivery of Recombinant Proteins and In Vitro Transcribed mRNAs for Protein Replacement Therapy of Human Severe Genetic Mitochondrial Disorders: The Case of Sco2 Deficiency.

    Published in:
    Pharmaceutics, 2023, v. 15, n. 1, p. 286, doi. 10.3390/pharmaceutics15010286
    By:
    • Miliotou, Androulla N.;
    • Foltopoulou, Parthena F.;
    • Ingendoh-Tsakmakidis, Alexandra;
    • Tsiftsoglou, Asterios S.;
    • Vizirianakis, Ioannis S.;
    • Pappas, Ioannis S.;
    • Papadopoulou, Lefkothea C.
    Publication type:
    Article
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