scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1365-2362.1989.TB00262.X |
P698 | PubMed publication ID | 2511024 |
P2093 | author name string | Breimer DD | |
Schellens JH | |||
van der Wart JH | |||
van der Velde EA | |||
Janssens AR | |||
P2860 | cites work | The disposition of antipyrine and its metabolites in young and elderly healthy volunteers | Q34416893 |
Relationship between the metabolism of antipyrine, hexobarbitone and theophylline in man as assessed by a 'cocktail' approach | Q34418061 | ||
Pharmacokinetics of theophylline: a dose-range study | Q34511493 | ||
Antipyrine clearance and metabolite formation in patients with alcoholic cirrhosis | Q42040905 | ||
Theophylline kinetics in relation to age: the importance of smoking | Q43243670 | ||
Histological changes in the liver and indices of drug metabolism in alcoholics | Q44785965 | ||
Fitting straight lines when both variables are subject to error | Q52795595 | ||
Overnight salivary caffeine clearance: a liver function test suitable for routine use. | Q53692613 | ||
P433 | issue | 5 | |
P304 | page(s) | 472-479 | |
P577 | publication date | 1989-10-01 | |
P1433 | published in | European Journal of Clinical Investigation | Q15745208 |
P1476 | title | Relationship between the metabolism of antipyrine, hexobarbital and theophylline in patients with liver disease as assessed by a 'cocktail' approach | |
P478 | volume | 19 |
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Q34346052 | Liver blood flow, antipyrine clearance, and antipyrine metabolite formation clearance in patients with chronic active hepatitis and alcoholic cirrhosis |
Q47722127 | Selective effect of liver disease on the activities of specific metabolizing enzymes: investigation of cytochromes P450 2C19 and 2D6. |
Q30963437 | Solid phase extraction and simultaneous high performance liquid chromatographic determination of antipyrine and its major metabolites in urine |
Q70490332 | The relationship between phenazone (antipyrine) metabolite formation and theophylline metabolism in healthy and frail elderly women |
Q73846452 | Validation of the five-drug "Pittsburgh cocktail" approach for assessment of selective regulation of drug-metabolizing enzymes |
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