ENZYMOLOGICAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1 BY MEASUREMENT OF HEPATIC ALANINE: GLYOXYLATE AMINOTRANSFERASE ACTIVITY
- 1 February 1987
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 329 (8528), 289-291
- https://doi.org/10.1016/s0140-6736(87)92023-x
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type IFEBS Letters, 1986
- Peroxisome localized human hepatic alanine-glyoxylate aminotransferase and its application to clinical diagnosisClinical Biochemistry, 1985
- The effect of vitamin B6 deficiency on alanine:Glyoxylate aminotransferase isoenzymes in rat liverArchives of Biochemistry and Biophysics, 1984
- Peroxisomal localization of alanine: Glyoxylate aminotransferase in human liverArchives of Biochemistry and Biophysics, 1979
- Isolation and characterization of a glutamate-glycine transaminase from human liverArchives of Biochemistry and Biophysics, 1966
- The metabolic error in primary hyperoxaluria.Archives of Disease in Childhood, 1965
- Studies on Primary HyperoxaluriaNew England Journal of Medicine, 1963
- RENAL CALCULI ASSOCIATED WITH HYPEROXALURIA*Annals of the New York Academy of Sciences, 1963
- Clinical Manifestations of Primary HyperoxaluriaArchives of Disease in Childhood, 1960
- FURTHER OBSERVATIONS ON THE GENETIC BASIS OF PRIMARY HYPEROXALURIAAnnals of Human Genetics, 1959