Authors: Karadimas, C Tanji, K Geremek, M Chronopoulou, P Vu, T Krishna, S Sue, CM Shanske, S Bonilla, E DiMauro, S Lipson, M Bachman, R

Citation: C. Karadimas et al., A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy, J CHILD NEU, 16(7), 2001, pp. 531-533

Authors: Panas, M Kalfakis, N Karadimas, C Vassilopoulos, D

Citation: M. Panas et al., Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene, NEUROLOGY, 57(10), 2001, pp. 1906-1908

Authors: Gamez, J Navarro, C Andreu, AL Fernandez, JM Palenzuela, L Tejeira, S Fernandez-Hojas, R Schwartz, S Karadimas, C DiMauro, S Hirano, M Cervera, C

Citation: J. Gamez et al., Autosomal dominant limb-girdle muscular dystrophy - A large kindred with evidence for anticipation, NEUROLOGY, 56(4), 2001, pp. 450-454

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: Giuffre, G Karadimas, C Kelley, R Mulready, M

Citation: G. Giuffre et al., Copolyester resin technology, ADHES AGE, 42(12), 1999, pp. 28

Authors: Panas, M Karadimas, C Avramopoulos, D Vassilopoulos, D

Citation: M. Panas et al., Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations, J NE NE PSY, 65(6), 1998, pp. 947-948