Acute peripheral neuropathy, rhabdomyolysis, and severe lactic acidosis associated with 3243 A to G mitochondrial DNA mutation.

Author:

Hara H,Wakayama Y,Kouno Y,Yamada H,Tanaka M,Ozawa T

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference5 articles.

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

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