BIOCHEMICAL ABNORMALITIES IN LEIGH'S DISEASE
- 5 June 1976
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 307 (7971) , 1237-1238
- https://doi.org/10.1016/s0140-6736(76)92181-4
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
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- Specificity of the urine inhibitor test for Leigh's diseaseNeurology, 1974
- Subdural empyema in infants, children and adultsNeurology, 1973
- Biochemical studies and therapy in subacute necrotizing encephalomyelopathy (Leigh's syndrome)The Journal of Pediatrics, 1972
- Pathogenesis of Leigh's encephalomyelopathyThe Journal of Pediatrics, 1972
- Subacute Necrotizing Encephalomyelopathy (Leigh's Disease): a Consideration of Clinical Features and EtiologyDevelopmental Medicine and Child Neurology, 1972
- A defect in pyruvate decarboxylase in a child with an intermittent movement disorderJournal of Clinical Investigation, 1970
- Thiamine Triphosphate Deficiency in Subacute Necrotizing EncephalomyelopathyScience, 1969
- Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.Archives of Disease in Childhood, 1968
- SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANTJournal of Neurology, Neurosurgery & Psychiatry, 1951