Litiasis purínicas infrecuentes: déficit de adenina fosforribosiltransferasa y xantinuria hereditaria

Author:

Antonio Orts Costa Juan,Zúñiga Cabrera Ángel,Ferrando Monleón Susana

Publisher

Elsevier BV

Subject

General Medicine

Reference87 articles.

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2. Uric acid provides antioxidant defense in humans against oxidant -and radical- caused aging and cancer: a hypothesis;Ames;Proc Nat Acad Sci,1981

3. Purine enzyme defects as a cause of acute renal failure in childhood;Simmonds;Pediatric Nephrology,1989

4. Xanthine oxidoreductase –role in human patophysiology and in hereditary xanthinuria;Raivio,2001

5. When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indications;Simmonds;J Inher Metab Dis,1997

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Identificación de una nueva mutación en el gen humano xantina causante de la xantinuria tipo I;Advances in Laboratory Medicine / Avances en Medicina de Laboratorio;2021-11-10

2. Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type I;Advances in Laboratory Medicine / Avances en Medicina de Laboratorio;2021-07-21

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