aminopyrine has been researched along with Hyperbilirubinemia, Hereditary in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (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 |
---|---|
Bar-Meir, S; Bartal, L; Gilat, T; Halpern, Z; Levy, R | 1 |
Bircher, J; Küpfer, A; Platzer, R; Preisig, R | 1 |
Bar-Meir, S; Bar-Tal, L; Papa, MZ; Peled, Y | 1 |
Dunn, D; Gray, JP; Hoyumpa, AM; Meredith, CG; Muhoberac, BB; Schenker, S; Speeg, KV | 1 |
4 other study(ies) available for aminopyrine and Hyperbilirubinemia, Hereditary
Article | Year |
---|---|
Aminopyrine breath test in Dubin Johnson and Gilbert's syndromes.
Topics: Aminopyrine; Breath Tests; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Jaundice, Chronic Idiopathic | 1982 |
Polymorphic acetylation and aminopyrine demethylation in Gilbert's syndrome.
Topics: Acetylation; Adult; Aminopyrine; Dealkylation; Female; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Kinetics; Male; Middle Aged; Phenotype; Sulfamethazine | 1978 |
Bromsulfophthalein clearance and aminopyrine test in patients with Gilbert's syndrome.
Topics: Adolescent; Adult; Aged; Aminopyrine; Breath Tests; Female; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Liver; Male; Middle Aged; Sulfobromophthalein | 1986 |
Hepatic oxidative drug metabolism and the microsomal milieu in a rat model of congenital hyperbilirubinemia.
Topics: Aminopyrine; Aminopyrine N-Demethylase; Animals; Bilirubin; Breath Tests; Cell Membrane; Cytochrome P-450 Enzyme System; Female; Hyperbilirubinemia, Hereditary; Kinetics; Male; Microsomes, Liver; Rats; Rats, Gunn | 1986 |