Excretion of Hypoxanthine and Xanthine in a Genetic Disease of Purine Metabolism

This publication has 9 references indexed in Scilit:

• Genetics of an X-Linked Disorder of Uric Acid Metabolism and Cerebral Function
  Pediatric Research, 1967
• Session III: Secondary Hyperuricaemia: Allopurinol in the Prevention of Hyperuricaemia Secondary to the Treatmient of Neoplastic Diseases with Alkylating Agents, Adrenal Steroids, and Radiation Therapy
  Annals of the Rheumatic Diseases, 1966
• Session I: Biochemistry and Metabolism: Effects of Alloplurnol in Relation to Purine Biosynthesis
  Annals of the Rheumatic Diseases, 1966
• Effect of allopurinol (4-Hydroxypyrazolo-(3,4-d)pyrimidine) on serum and urinary uric acid in primary and secondary gout
  The American Journal of Medicine, 1964
• A familial disorder of uric acid metabolism and central nervous system function
  The American Journal of Medicine, 1964
• Xanthinuria and Hemochromatosis
  New England Journal of Medicine, 1964
• Augmentation of the incorporation of hypoxanthine into nucleic acids by the administration of an inhibitor of xanthine oxidase
  Biochimica et Biophysica Acta (BBA) - Specialized Section on Nucleic Acids and Related Subjects, 1963
• ON THE MECHANISM OF OVERPRODUCTION OF URIC ACID IN PATIENTS WITH PRIMARY GOUT1
  Journal of Clinical Investigation, 1958
• Enzymic Determination of Hypoxanthine and Xanthine in Human Plasma and Urine.
  Acta Pharmacologica et Toxicologica, 1955