507 results on '"Back DJ"'
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2. A call for a consortium for optimal management of drug–drug interactions in patient care
3. Comparison of dried blood spots versus conventional plasma collection for the characterization of efavirenz pharmacokinetics in a large-scale global clinical trial-the ENCORE1 study
4. Pharmacokinetics of plasma lopinavir/ritonavir following the administration of 400/100, 200/150, and 200/50 mg twice daily in HIV‐negative volunteers
5. Therapeutic drug monitoring (TDM) of atazanavir in pregnancy
6. Evaluating pharmacist involvement in HIV outpatient clinics: can medication histories, drug interaction checks and adherence assessments add benefit?
7. The pharmacokinetic and safety profile of raltegravir and ribavirin, when dosed separately and together, in healthy volunteers
8. A population pharmacokinetic model confirms an association between a pregnane-X-receptor (PXR) polymorphism and unboosted atazanavir clearance
9. Therapeutic drug monitoring of atazanavir/ritonavir in pregnancy
10. The unbound percentage of saquinavir and indinavir remains constant throughout the dosing interval in HIV positive subjects
11. Undefined duration of opiate withdrawal induced by efavirenz in drug users with HIV infection and undergoing chronic methadone treatment
12. HIV therapy in an ageing population- the challenge of polypharmacy
13. SLCO3A1 expression is a major determinant of atazanavir PBMC penetration in HIV-infected patients
14. Therapeutic drug monitoring of lopinavir/ritonavir in pregnancy
15. The use of a darunavir/ritonavir once-daily regimen in two pregnant women
16. Population pharmacokinetic modelling of once-daily ritonavir-boosted darunavir in HIV-infected patients
17. Cytochrome P450 2B6 516G→T is associated with plasma concentrations of nevirapine at both 200 mg twice daily and 400 mg once daily in an ethnically diverse population
18. The impact of cytokines on the expression of drug transporters, cytochrome P450 enzymes and chemokine receptors in human PBMC
19. A study to evaluate the efficacy, safety and tolerability of co-administered lopinavir/ritonavir (LPVr) and nevirapine (NVP) in HIV-infected adults
20. O122 Prevalence of drug interactions between antiretroviral and co-administered drugs at the Moi teaching and referral hospital (Ampath), Eldoret, Kenya
21. Plasma concentrations of boosted and unboosted atazanavir are predicted by 63396C>T SNP in the PXR gene
22. Lopinavir is a substrate for SLCO1A2 but 516A>C and 38T>C polymorphisms do not influence lopinavir plasma concentrations
23. An open-label multicentre pilot study evaluating the pharmacokinetics (PK) of co-administered lopinavir (LPV) and nevirapine (NVP) in HIV+ adults
24. Frequency of functional drug disposition gene polymorphism in Thai population: relevance to antiretroviral drugs
25. Correlation between Intracellular Pharmacological Activation of Nucleoside Analogues and HIV Suppression in Vitro
26. Current uses and future hopes for clinical pharmacology in the management of HIV infection
27. Zidovudine therapy in HIV infection: which patients should be treated and when.
28. Effects of dideoxyinosine and dideoxycytidine on the intracellular phosphorylation of zidovudine in human mononuclear cells.
29. Pharmacokinetics of zidovudine and dideoxyinosine alone and in combination in patients with the acquired immunodeficiency syndrome.
30. Zidovudine pharmacokinetics in zidovudine-induced bone marrow toxicity.
31. Cyclosporin metabolism by human gastrointestinal mucosal microsomes.
32. Metabolism of 2′,3′-dideoxyinosine (ddI) in human blood.
33. Extrahepatic metabolism of zidovudine.
34. Factors affecting the enterohepatic circulation of oral contraceptive steroids
35. The effect of metoclopramide on mefloquine pharmacokinetics [letter]
36. Gastrointestinal metabolism of contraceptive steroids
37. Comparative effects of the antimycotic drugs ketoconazole, fluconazole, itraconazole and terbinafine on the metabolism of cyclosporin by human liver microsomes.
38. The effect of various drugs on the glucuronidation of zidovudine (azidothymidine; AZT) by human liver microsomes.
39. Cytochrome P450 2B6 516G --<GT>T is associated with plasma concentrations of nevirapine at both 200 mg twice daily and 400 mg once daily in an ethnically diverse population [corrected] [published erratum appears in HIV MED 2009 Nov;10(10):661].
40. Cyclosporin metabolism by the gastrointestinal mucosa.
41. The interaction of phenytoin and carbamazepine with combined oral contraceptive steroids.
42. Azoles and allylamines: the clinical implications of interaction with cytochrome P-450 enzymes
43. A longitudinal study of maternal dose response to low molecular weight heparin in pregnancy.
44. Calcium channel antagonists and cyclosporine metabolism: in vitro studies with human liver microsomes.
45. Comparative effects of two antimycotic agents, ketoconazole and terbinafine on the metabolism of tolbutamide, ethinyloestradiol, cyclosporin and ethoxycoumarin by human liver microsomes in vitro.
46. Metabolism of the contraceptive steroid desogestrel by the intestinal mucosa.
47. In vitro inhibition studies of tolbutamide hydroxylase activity of human liver microsomes by azoles, sulphonamides and quinolines.
48. Evaluation of Committee on Safety of Medicines yellow card reports on oral contraceptive-drug interactions with anticonvulsants and antibiotics.
49. Tolbutamide 4-hydroxylase activity of human liver microsomes: effect of inhibitors.
50. Intestinal metabolism of ethinyloestradiol and paracetamol in vitro: studies using Ussing chambers.
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