原尚子 | 大阪大学医学部第二内科

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著作論文

Two brothers with hereditary xanthinuria due to xanthine oxidase deficiency
A family of hereditary xanthinuria: Two siblings with peptic ulcer and hypouricemia due to xanthine oxidase deficinecy, and a heterozygote(father) with gout.
Purine Degradation in Contracting Fast and Slow Muscle
Enhanced purine degradation in muscles of patients with hypoparathyroidism
A Contribution of Hepatic Purine Degradation Induced by Hypoglycemia to the Development of Hyperuricemia in Glycogen Storage Disease Type I
A case of renal hypouricemia associated with increased plasma oxypurine concentration due to its decreased excretion
Overproduction of oxypurines through myogenic and hepatogenic mechanisms
Pathogenesis of Hyperuricemia in Type VII Glycogenosis:an accelerated purine degradation in exercising muscle
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
Myogenic Hyperuricemia: a novel mechanism of hyperuricemia found in type VII glycogenosis

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