Pyruvate carboxylase deficiency, studies on patients and on an animal model system-Reference-Cited by-同舟云学术

Pyruvate carboxylase deficiency, studies on patients and on an animal model system

Published:1980 Issue: Volume: Page:269-286
ISSN:
Container-title:Inherited Disorders of Carbohydrate Metabolism
language:
Short-container-title:

Author:

Hommes F. A.,Schrijver J.,Dias Th.

Publisher

Springer Netherlands

Link

http://link.springer.com/content/pdf/10.1007/978-94-009-9215-3_16.pdf

Reference67 articles.

1. R. M. Denton, (1979). Pathways and regulation of pyruvate metabolism. This volume, p. 209

2. J. M. Land and J. B. Clark, (1975). The changing pattern of brain mitochondrial substrate utilization during development. In F. A. Hommes and C. J. van den Berg (eds.). Normal and Pathological Development of Energy Metabolism, pp. 155–167. (Academic Press London)

3. D. Leigh, (1951). Subacute necrotizing encephalomyelopathy in an infant. J. Neurol. Neurosurg. Psychiatry, 14, 216

4. J. P. Blass, S. D. Cederbaum and H. G. Dunn, (1976). Biochemical abnormalities in Leigh’s disease. Lancet, 1, 1237

5. J. R. Cooper, Y. Itokawa and J. H. Pincus, (1969). Thiamin triphosphate deficiency in subacute necrotizing encephalomyelopathy. Science, 164, 72

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