Literature DB >> 2319729

Deficient benzbromarone elimination: a familial disorder?

N Zöllner1, U Gresser, I Walter-Sack.   

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Year:  1990        PMID： 2319729     DOI： 10.1007/bf01646852

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN： 0023-2173


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  1 in total

1.  Benzbromarone disposition and uricosuric action; evidence for hydroxilation instead of debromination to benzarone.

Authors:  I Walter-Sack; J X de Vries; A Ittensohn; M Kohlmeier; E Weber
Journal:  Klin Wochenschr       Date:  1988-02-15
  1 in total
  3 in total

1.  Rapid and slow benzbromarone elimination phenotypes in man: benzbromarone and metabolite profiles.

Authors:  I Walter-Sack; J X de Vries; A Ittensohn; E Weber
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

2.  Variation of benzbromarone elimination in man--a population study.

Authors:  I Walter-Sack; U Gresser; M Adjan; I Kamilli; A Ittensohn; J X de Vries; E Weber; N Zöllner
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

3.  Benzbromarone hydroxylation in man: defective formation of the 6-hydroxybenzbromarone metabolite.

Authors:  J X de Vries; I Walter-Sack; A Ittensohn; E Weber; H Empl; U Gresser; N Zöllner
Journal:  Clin Investig       Date:  1993-11
  3 in total

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