Organic Acids in Urine of Patients with Congenital Lactic Acidoses: An Aid to Differential Diagnosis
Publisher
Springer Netherlands
Reference33 articles.
1. Atkin, B. M., Buist, N. R. M., Utter, M. F., Leiter, A. B. and Banker, B. Q. Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh’s disease. Pediatr. Res. 13 (1979) 109–116. 2. Baal, M. G., Gabreëls, F. J. M., Renier, W. O., Hommes, F. A., Gijsbers, Th. H. J., Lamars, K. J. B. and Kok, J. C. N. A patient with pyruvate carboxylase deficiency in the liver: Treatment with aspartic acid and thiamine. Dev. Med. Child Neurol. 23 (1981) 521–530. 3. Burman, D., Holton, J. B. and Pennock, C. A. Inherited Disorders of Carbohydrate Metabolism, MTP Press, Lancaster, 1980. 4. Cederbaum, S. D., Blass, J. P., Minkoff, N., Brown, W. J., Cotton, M. E. and Harris, S. H. Sensitivity to carbohydrate in a patient with familial intermittant lactic acidosis and pyruvate dehydrogenase deficiency. Pediatr. Res. 10 (1976) 713–720. 5. Chalmers, R. A. and Lawson, A. M. Organic Acids in Man. The Analytical Chemistry, Biochemistry and Diagnosis of the Organic Acidurias, Chapman&Hall, London, 1982.
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