Morgan P, Hoppel CL, Sedensky MM. Mitochondrial defects and anesthetic sensitivity. Anesthesiology 2002; 96: 1268–1270.
Plasterer TN, Smith TF, Mohr SC. Survey of human mitochondrial diseases using new genomic/proteomic tools. Gene Biol 2001; 2: 1–16.
Solano A, Playan A, Loez-Perez MJ, Montoya J. Genetic diseases of the mitochondrial DNA in humans. Salud Publica Mexico 2001; 43: 151–161.
Rosaeg OP, Morrison S, MacLeod JP. Anaesthetic management of labour and delivery in the parturient with mitochondrial myopathy. Can J Anaesth 1996; 43: 403–407.
Mehndiratta MM, Agarwal P, Tatke M, Krishnamurthy M. Neurological mitochondrial cytopathies. Neurol India 2002; 50: 162–167.
Wisely NA, Cook PR. General anaesthesia in a man with mitochondrial myopathy undergoing eye surgery. Eur J Anaesthesiol 2001; 18: 333–335.
Hsiao PN, Cheng TJ, Tseng HC, Chuang YH, Kao PF, Tsai SK. Spinal anesthesia in MELAS syndrome: a case with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes. Acta Anaesthesiol Sin 2000; 38: 107–110.
Wredenberg A, Wibom R, Wilhelmsson H, et al. Increased mitochondrial mass in mitochondrial myopathy mice. Proc Natl Acad Sci USA 2002; 99: 15066–15071.
Schapira AH. Mitochondrial disorders. Biochem Biophys Acta 1999; 1410: 99–102.
Wallace JJ, Perndt H, Skinner M. Anaesthesia and mitochondrial disease. Paediatr Anaesth 1998; 8: 249–254.
Ciccotelli KK, Prak EL, Muravchick S. An adult with inherited mitochondrial encephalopathy: report of a case. Anesthesiology 1997; 87: 1240–1242.
Cheam EWS, Critchley LAH. Anesthesia for a child with complex I respiratory chain enzyme deficiency. J Clin Anesth 1998; 10: 524–527.
Dalta V, Jain P, Mehndirrata MM, et al. Myoclonic epilepsy with red ragged fibres. Indian Pediatr 1999; 36: 817–819.
Nouette-Gaulain K, Forestier F, Malgat M, Marthan R, Mazat JP, Sztark F. Effects of bupivacaine on mitochondrial energy metabolism in heart of rats following exposure to chronic hypoxia. Anesthesiology 2002; 97: 1507–1511.
Farag E, Argalious M, Narouze S, DeBoer G, Tome J. The anesthetic management of ventricular septal defect (VSD) repair in a child with mitochondrial cytopathy. Can J Anaesth 2002; 49: 958–962.
Thompson VA, Wahr JA. Anesthetic considerations in patients presenting with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome. Anesth Analg 1997; 85: 1404–1406.
Sharma AD, Erb E, Schulman SR, Sreeram G, Slaughter TF. Anaesthetic considerations for a child with combined Prader–Willi syndrome and mitochondrial myopathy. Paediatr Anaesth 2001; 11: 488–490.
Taivassalo T, Abbott A, Wyrick P, Haller RG. Venous oxygen levels during aerobic forearm exercise: and index of impaired oxidative metabolism in mitochondrial myopathy. Ann Neurol 2002; 51: 38–44.
Ohtani Y, Miike T, Ishitsu T, et al. A case of malignant hyperthermia with mitochondrial dysfunction. Brain Dev 1985; 7: 249.
Steensberg A, Vissing J, Pedersen BK. Lack of IL-6 production during exercise in patients with mitochondrial myopathy. Eur J Appl Physiol 2001; 84: 155–157.
Vladutiu GD, Bennett MJ, Smail D, Wong LJ, Taggart RT, Lindsley HB. A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene. Mol Genet Metab 2000; 70: 134–141.