Hereditary xanthinuria presenting in infancy with nephrolithiasis
- 31 August 1986
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 109 (2) , 307-309
- https://doi.org/10.1016/s0022-3476(86)80391-2
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?Journal of Inherited Metabolic Disease, 1978
- Hereditary XanthinuriaNephron, 1977
- Urinary Excretion of 6 Hydroxylated Metabolite and Oxypurines in a Xanthinuric Man Given Allopurinol or ThiopurinolPublished by Springer Nature ,1974
- A comparison of the specificities of xanthine oxidase and aldehyde oxidaseArchives of Biochemistry and Biophysics, 1972
- Urinary excretion of purines, pyrimidines and pyrazolopyrimidines in patients treated with allopurinol or oxipurinolClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- Clinical, physiological and biochemical studies of a patient with xanthinuria and pheochromocytomaThe American Journal of Medicine, 1964