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Results: 3

Authors: Sue, CM Karadimas, C Checcarelli, N Tanji, K Papadopoulou, LC Pallotti, F Guo, FL Shanske, S Hirano, M De Vivo, DC Van Coster, R Kaplan, P Bonilla, E DiMauro, S
Citation: Cm. Sue et al., Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2, ANN NEUROL, 47(5), 2000, pp. 589-595

Authors: Papadopoulou, LC Sue, CM Davidson, MM Tanji, K Nishino, I Sadlock, JE Krishna, S Walker, W Selby, J Glerum, DM Van Coster, R Lyon, G Scalais, E Lebel, R Kaplan, P Shanske, S De Vivo, DC Bonilla, E Hirano, M DiMauro, S Schon, EA
Citation: Lc. Papadopoulou et al., Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene, NAT GENET, 23(3), 1999, pp. 333-337

Authors: Papadopoulou, LC Theophilidis, G Thomopoulos, GN Tsiftsoglou, AS
Citation: Lc. Papadopoulou et al., Structural and functional impairment of mitochondria in adriamycin-inducedcardiomyopathy in mice: Suppression of cytochrome c oxidase II gene expression, BIOCH PHARM, 57(5), 1999, pp. 481-489
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