Literature DB >> 4369449

Xanthine oxidase deficiency: studies of a previously unreported case.

E W Holmes, D H Mason, L I Goldstein, R E Blount, W N Kelley.   

Abstract

Mesh：

Substances：

Year:  1974        PMID： 4369449

Source DB:  PubMed          Journal:  Clin Chem        ISSN： 0009-9147            Impact factor:   8.327


× No keyword cloud information.
  4 in total

1.  Xanthinuria type I: a rare cause of urolithiasis.

Authors:  Nina Arikyants; Ashot Sarkissian; Albrecht Hesse; Thomas Eggermann; Ernst Leumann; Beat Steinmann
Journal:  Pediatr Nephrol       Date:  2006-11-09       Impact factor: 3.714

2.  Hereditary xanthinuria. Evidence for enhanced hypoxanthine salvage.

Authors:  F A Mateos; J G Puig; M L Jiménez; I H Fox
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

3.  Allopurinol metabolism in a patient with xanthine oxidase deficiency.

Authors:  H Yamanaka; K Nishioka; T Suzuki; K Kohno
Journal:  Ann Rheum Dis       Date:  1983-12       Impact factor: 19.103

4.  A purine auxotroph deficient in phosphoribosylpyrophosphate amidotransferase and phosphoribosylpyrophosphate aminotransferase activities with normal activity of ribose-5-phosphate aminotransferase.

Authors:  E W Holmes; G L King; A Leyva; S C Singer
Journal:  Proc Natl Acad Sci U S A       Date:  1976-07       Impact factor: 11.205
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.