共 14 条
[1]
Feely, Practical Clinical Pharmacology: drug handling and response, Br. Med. J., 296, pp. 1046-50, (1988)
[2]
Clark D.W., Genetically determined variability in acetylalion and oxidation: therapeutic implications, Drugs, 29, pp. 342-75, (1985)
[3]
Price-Evans D., An improved and simplified method of detecting acetylator phenotype, J. Med. Genet., 6, pp. 405-7, (1969)
[4]
Lennard M.S., Silas J.H., Smith A.J., Tucker G.T., Determination of debrisoquine and its 4-hydroxy metabolite in biological fluids by gas chromatography with flame-ionization and nitrogen-selective detectino, J. Chromatog, 133, pp. 161-166, (1977)
[5]
Mahgoub A., Idle J.R., Dring L.G., Lancaster R., Smith R.L., Polymorphic hydroxylation of debrisoquine in man, Lancet, 2, pp. 584-586, (1977)
[6]
Idle J.R., Oates N.S., Shah R.R., Smith R.L., Protecting poor metabolisers a group at high risk of adverse drug reactions, Lancet, 1, (1983)
[7]
Brosen K., Klysner R., Gram L.F., Otton S.V., Bech P., Bertillsson L., Steady state concentrations of imipramine and its metabolites in relation to the sparteine/debrisoquine polymorphism, European Journal of Clinical Pharmacology, 30, pp. 679-684, (1986)
[8]
Brosen K., Hagfelt L.F., Bertillsson T., Gram L., Extensive metabolisers of debrisoquine become poor metabolisers during quinidine treatment, Pharmac. Tox., 60, pp. 312-314, (1987)
[9]
Speirs J., Murray, Seddon C.E., Davies D.S., Quinidine and the identification of drugs whose elimination is impaired in subjects classified as poor metabolisers of debrisoquine, Br. J. Clin. Pharmacol, 22, pp. 739-734, (1986)
[10]
Leeman T., Dayer P., Meyer U.A., Single dose quinidine treatment inhibits metoprolol oxidation in extensive metabolisers, European Journal of Clinical Pharmacology, 29, pp. 739-741, (1986)