1. Mitochondrial DNA mutation in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode (MELAS);Tanaka, M.; Ino, H.; Ohno, K.;Biochem Biophys Res Commun,1991
2. Neuropathy and mitochondrial myopathy;Peyronnard, J.-M.; Charron, L.; Bellavance, A.; Marchand, L.;Ann Neurol,1980
3. Peripheral neuropathy associated with mitochondrial myopathy;Yannikas, C.; McLeod, J.G.; Pollard, J.D.; Baverstock, J.;Ann Neurol,1986
4. Lactic acidemia, mitochondrial myopathy, and basal gangria calcification;Markesbery, W.R.;Neurology,1979
5. Pathological findings of the soupraatlhyn.ervJepnin mitochondrial encephalomy7 Psychiatr;Katsuragi, S.; Shimoji, A.; Watanabe, K.; Miyakawa, T.;Neurol,1988