Concepedia

Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: Correlation with pyridoxine responsiveness

R. J. A. Wanders, C. W. T. van Roermund, Suzanne Jurriaans, R. B. H. Schutgens, Joseph M. Tager, H. van den Bosch, E. D. Wolff, Hildegard Przyrembel, R. Berger, F. G. Schaaphok,

Journal of Inherited Metabolic Disease · 1988 · 13 citations · 6 references

DOI

Concepts

References

6

The Metabolic Basis of Inherited Disease.

Annals of Internal Medicine · 1988 · 7.8K citations

, , +13

The Metabolic Basis of Inherited Disease

Matthew D. Crawford · Journal of Clinical Pathology · 1983 · 960 citations · Full text

, , +13

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

Christopher J. Danpure, Patricia R. Jennings · FEBS Letters · 1986 · 347 citations

, , +16

ENZYMOLOGICAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1 BY MEASUREMENT OF HEPATIC ALANINE: GLYOXYLATE AMINOTRANSFERASE ACTIVITY

ChristopherJ. Danpure, PatriciaR. Jennings, RichardW.E. Watts · The Lancet · 1987 · 174 citations

, , +12

Glycolate and Glyoxylate Metabolism by Isolated Peroxisomes or Chloroplasts

Takuro Kisaki, N. E. Tolbert · PLANT PHYSIOLOGY · 1969 · 151 citations · Full text

, , +17