References
Axelrod FB, Chelimsky G, Weese-Mayer DE. Pediatric autonomic disorders. Pediatrics 2006;118:309-21.
Bennett MJ, Sherwood WG, Gibson KM, Burlina AB. Secondary inhibition of multiple NAD-requiring dehydogenases in respiratory complex I deficiency: Possible metabolic markers for the primary defect. J Inher Metab Dis 1993;16:560-62.
Davis MD, Sandroni P, Rooke T, Low P. Arch Derm 2002;139(10):1337-43.
Enns GM, Bennett MJ, Hoppel CL, et al. Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long chain 3-hydoxyacyl-coenzyme A dehydrogenase deficiency. J Pediatr 2000;136:251-4.
Hagenfeldt L. Compromised fatty acid oxidation in mitochondrial disorders. J Inher Metab Dis 1998;21(5):613-7.
Kang HC, Lee YM, Kim HD, et al. Safe and effective use of the ketogenic diet in children with epilepsy and mitochondrial respiratory chain complex defects. Epilepsia 2007;48(1):82-8.
Sembrano E, Barthlen GM, Wallace S, Lamm C. Polysomnographic findings in a patient with the mitochondrial encephalomyopathy NARP. Neurology 1997;49:1714-7.
Wexler ID, Hemalatha SG, McConnell J, et al. Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets: Studies in patients with identical mutations. Neurology 1997:49(6):1655-61.
Yasaki E, Saito Y, Nakano K, et al. Characteristics of breathing abnormality in
Leigh and its overlap syndromes. Neuropediatrics 2001;32(6):299-306.
Zelnik N, Axelrod FB, Leschinsky E, et al. Mitochondrial encephalomyopathies presenting with features of autonomic and visceral dysfunction. Pediatr Neurol 1996;14:251-4.




