清川裕朗 | 大阪大学医学部第二内科

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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
A case of renal hypouricemia associated with increased plasma oxypurine concentration due to its decreased excretion
A case of renal hypouricemia with Parkinsonism
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

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