嶺尾郁夫 | 大阪大学医学部第二内科

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家族性地中海熱型を呈しコルヒチンが奏効した周期熱の1例
Two brothers with hereditary xanthinuria due to xanthine oxidase deficiency
Molecular biological approaches to the mechanism of myogenic hyperuricemia: analysis of the primary structure and the genomic structure of muscle - type isozyme of human phosphofructokinase
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
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
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
Molecular Basis of Myogenic Hyperuricemia:Analysis of Tissue-specific Expression of Phosphofructokinase-M Gene Transcripts
Treatment of Myogenic Hyperuricemia:Allopurinol Effects in Muscle Phosphofructokinase Deficiency
A Case of Hypouricemia due to Combined Reabsorption Defect
Three cases of renal hypouricemia
Family study of hereditary xanthine (xanthine oxidase deficiency ):increased urinary excretions of xanthine and hypoxanthine in heterozygotes and association with gout in a heterozygote
Pathogenesis of Hyperuricemia in Glycogenosis Type VII:a contribution of an exaggerated degradation of purine nucleotides in exercising muscle
Adult Case of Glycogenosis Type I with Hyperuricemia
Myogenic Hyperuricemia: a novel mechanism of hyperuricemia found in type VII glycogenosis

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