川知雅典 | 大阪大学医学部第二内科

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著作論文

A family of hereditary xanthinuria: Two siblings with peptic ulcer and hypouricemia due to xanthine oxidase deficinecy, and a heterozygote(father) with gout.
Hypouricemia associated with hyperoxypurinemia due to altered renal handling - Analysis by probenecid - and pyrazinamide - loading tests
Purine Degradation in Contracting Fast and Slow Muscle
Enhanced purine degradation in muscles of patients with hypoparathyroidism
Effect of Daily Consumption Dose of Ethanol on the Ethanol Induced Hyperuricemia
A Contribution of Hepatic Purine Degradation Induced by Hypoglycemia to the Development of Hyperuricemia in Glycogen Storage Disease Type I
Treatment of myogenic hyperuricemia:Effects of glucose infusion and allopurinol administration on purine metabolism in patients with muscular glycogenoses
A case of renal hypouricemia associated with increased plasma oxypurine concentration due to its decreased excretion
Overproduction of oxypurines through myogenic and hepatogenic mechanisms
A case of renal hypouricemia with Parkinsonism
Treatment of Myogenic Hyperuricemia:Allopurinol Effects in Muscle Phosphofructokinase Deficiency
Family study of hereditary xanthine (xanthine oxidase deficiency ):increased urinary excretions of xanthine and hypoxanthine in heterozygotes and association with gout in a heterozygote
Exercise- induced alteration of erythrocyte glycolysis -Its relation to accelerated degradation of muscular adenine nucleotides
Myogenic Hyperuricemia: a novel mechanism of hyperuricemia found in type VII glycogenosis

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