Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.

Author:

Yamamoto M,Sato T,Anno M,Ujike H,Takemoto M

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference20 articles.

1. Mitochondrial encephalopathy: a group of neuromuscular disorders with defects in oxidative metabolism;Shapira, Y.; Harel, S.; Russel, A.;Isr J Med Sci,1977

2. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinct clinical syndrome;Pavlakis, S.G.; Phillips, P.C.; Dimauro, S.;Ann Neurol,1984

3. Studies on cytochrome c I. Isolation, purification and properties of cytochrome c from beef heart muscle;Sekuzu, I.; Orii, Y.; Okunuki, K.;J Biochem

4. Wasserkurg HL el al. Non-droplet ultrastructural demonstration of cytochrome oxidase activity with a polymerising osmophilic reagent, diaminobenzidine (DAB);Seligman, A.M.; Karnovsky, M.J.;J Cell Biol,1968

5. Richardson SH, Hatefi Y. A rapid method for the preparation of highly purified cytochrome oxidase;Fowler, L.R.;Biochem Biophys Acta

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