1. Familial myoclonic epilepsy syndrome associated with skeletal muscle mitochondrial abnormalities;Tsairis;Neurology,1973
2. Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue;Willems;Pediatr.,1977
3. Rapid detection of the A–G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF);Zeviani;Am. J. Hum. Genet.,1991
4. 3-Nitropropionic acid is an indirect excitotoxin to cultured cerebellar granule neurons;Weller;Eur. J. Pharmacol.,1993
5. Cytochrome c oxidase-associated Leigh syndrome: Phenotypic features and pathogenetic speculations