tribuzone has been researched along with Hyperbilirubinemia, Hereditary in 1 studies
*Hyperbilirubinemia, Hereditary: Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cepelák, V; Mayer, O; Petera, V | 1 |
1 other study(ies) available for tribuzone and Hyperbilirubinemia, Hereditary
| Article | Year |
|---|---|
[Pharmacokinetics of tribuzone (Benetazone Spofa) in patients with Gilbert's syndrome (author's transl)].
Topics: Adult; Female; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Kinetics; Liver Cirrhosis; Male; Phenylbutazone | 1980 |