Page 120 - 80 guidelines for the treatment of malaria_opt
P. 120

nd
              Guidelines for the treatment of malaria – 2  edition


            51.   Mihaly GW et al. Pharmacokinetics of primaquine in man: identification of the carboxylic
                 acid derivative as a major plasma metabolite. British Journal of Clinical Pharmacology, 1984,
                 17:441–446.
            52.  Chan TK, Todd D, Tso SC. Drug-induced haemolysis in glucose-6-phosphate dehydrogenase
                 deficiency. British Medical Journal, 1976, 2:1227–1229.
            53.   McGready R et al. The pharmacokinetics of atovaquone and proguanil in pregnant
                 women with acute falciparum malaria. European Journal of Clinical Pharmacology, 2003,
                 59:545–552.
            54.  Sabchareon A et al. Efficacy and pharmacokinetics of atovaquone and proguanil in children
                 with multidrug-resistant Plasmodium falciparum malaria. Transactions of the Royal Society
                 of Tropical Medicine and Hygiene, 1998, 92:201–206.
            55.   Helsby NA et al. The pharmacokinetics and activation of proguanil in man: consequences of
                 variability in drug metabolism. British Journal of Clinical Pharmacology, 1990, 30:593–598.
            56.  Kaneko A et al. Proguanil disposition and toxicity in malaria patients from Vanuatu with
                 high frequencies of CYP2C19 mutations. Pharmacogenetics, 1999, 9:317–326.
            57.   Wattanagoon Y et al. Single dose pharmacokinetics of proguanil and its metabolites in
                 healthy subjects. British Journal of Clinical Pharmacology, 1987, 24:775–780.
            58.  Hussein Z et al. Population pharmacokinetics of proguanil in patients with acute P.
                 falciparum malaria after combined therapy with atovaquone. British Journal of Clinical
                 Pharmacology, 1996, 42:589–597.
            59.   Wangboonskul J et al. Single dose pharmacokinetics of proguanil and its metabolites in
                 pregnancy. European Journal of Clinical Pharmacology, 1993, 44:247–251.
            60.  McGready R et al. Pregnancy and use of oral contraceptives reduces the biotransformation
                 of proguanil to cycloguanil. European Journal of Clinical Pharmacology, 2003, 59:553–557.
            61.   Veenendaal JR, Edstein MD, Rieckmann KH. Pharmacokinetics of chlorproguanil in man
                 after a single oral dose of Lapudrine. Chemotherapy, 1988, 34:275–283.
            62.  White NJ et al. Quinine pharmacokinetics and toxicity in cerebral and uncomplicated
                 falciparum malaria. American Journal of Medicine, 1982, 73:564–572.
            63.   van Hensbroek MB et al. Quinine pharmacokinetics in young children with severe malaria.
                 American Journal of Tropical Medicine and Hygiene, 1996, 54:237–242.
            64.  Supanaranond W et al. Disposition of oral quinine in acute falciparum malaria. European
                 Journal of Clinical Pharmacology, 1991, 40:49–52.
            65.   Waller D et al. The pharmacokinetic properties of intramuscular quinine in Gambian
                 children with severe falciparum malaria. Transactions of the Royal Society of Tropical
                 Medicine and Hygiene, 1990. 84:488–491.
            66.  White NJ. Optimal regimens of parenteral quinine. Transactions of the Royal Society of
                 Tropical Medicine and Hygiene, 1995, 89:462–464.
            67.   Silamut K et al. Binding of quinine to plasma proteins in falciparum malaria. American
                 Journal of Tropical Medicine and Hygiene, 1985, 34:681–686.
            68.  Silamut K et al. Alpha 1-acid glycoprotein (orosomucoid) and plasma protein binding of
                 quinine in falciparum malaria. British Journal of Clinical Pharmacology, 1991, 32:311–315.


   106
   115   116   117   118   119   120   121   122   123   124   125