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