Hereditary xanthinuria with severe urolithiasis occurring in infancy as renal tubular acidosis and hypercalciuria
- 31 August 1989
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 115 (2) , 277-280
- https://doi.org/10.1016/s0022-3476(89)80083-6
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Urine Ammonium: The Key to the Diagnosis of Distal Renal Tubular AcidosisNephron, 1988
- Hereditary xanthinuria. Evidence for enhanced hypoxanthine salvage.Journal of Clinical Investigation, 1987
- Prenatal diagnosis of inborn errors of metabolism with renal manifestationsPediatric Nephrology, 1987
- Hereditary xanthinuria presenting in infancy with nephrolithiasisThe Journal of Pediatrics, 1986
- Renal tubular acidosis in childhoodKidney International, 1981
- Xanthine Oxidase Deficiency: Studies of a Previously Unreported CaseClinical Chemistry, 1974