Blass LP, Cederbaum SD, Dunn HG: Biochemical abnormalities in Leigh's disease. Lancet1976;1:1237-1238.
2.
Hommes FA, Polman HA, Reerink JD: Leigh's encephalomyelopathy: An inborn error of gluconeogenesis. Arch Dis Child1968;43:423-426.
3.
Miyabayashi S., Narisawa K., linuma K., et al: Cytochrome c oxidase deficiency in two siblings with Leigh encephalomyelopathy. Brain Dev1984;6:362-372.
4.
Miyabayashi S., Ito K., Narisawa K., et al: Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy . Eur J Pediatr1985;143:278-283.
5.
Sorbi S., Blass JP: Abnormal activation of pyruvate dehydrogenase in Leigh disease fibroblasts . Neurology1982;32:555-558.
6.
Willems JL, Monnens LAH, Trijbels JMF, et al: Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue. Pediatrics1977 ;60:850-857.
7.
Hall K., Gardner-Medwin D.: CT scan appearance in Leigh's disease (subacute necrotizing encephalomyelopathy) . Neuroradiology1978;6:48-50.
8.
Koch TK, Lo WD, Berg BO: Variability of serialCT scan in subacute necrotizing encephalomyelopathy (Leigh disease) . Pediatr Neurol1985;1:48-51.
9.
Schwartz WJ, Hutchinson HT, Berg BO: Computed tomography in subacute necrotizing encephalomyelopathy (Leigh disease) . Ann Neurol1981;10:268-271.
10.
Leigh D.: Subacute necrotizing encephalomyelopathy in an infant. J Neurol Neurosurg Psychiatry1951;14:216-221.
