Impact of inflammation and concomitant glucocorticoid administration on plasma concentration of triazole antifungals in immunocompromised patients.
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[1] H. Yamada,et al. Hydroxy-itraconazole pharmacokinetics is similar to that of itraconazole in immunocompromised patients receiving oral solution of itraconazole. , 2013, Clinica chimica acta; international journal of clinical chemistry.
[2] Y. Kagawa,et al. Impact of cachexia on pharmacokinetic disposition of and clinical responses to oxycodone in cancer patients , 2012, European Journal of Clinical Pharmacology.
[3] R. Bies,et al. Bioavailability and Population Pharmacokinetics of Voriconazole in Lung Transplant Recipients , 2010, Antimicrobial Agents and Chemotherapy.
[4] Kazuaki Matsumoto,et al. Correlation between voriconazole trough plasma concentration and hepatotoxicity in patients with different CYP2C19 genotypes. , 2009, International journal of antimicrobial agents.
[5] K. Ho,et al. An Update on C-reactive Protein for Intensivists , 2009, Anaesthesia and intensive care.
[6] Honghao Zhou,et al. The CYP2C19 ultra-rapid metabolizer genotype influences the pharmacokinetics of voriconazole in healthy male volunteers , 2009, European Journal of Clinical Pharmacology.
[7] D. Andes,et al. Therapeutic drug monitoring of antifungals: pharmacokinetic and pharmacodynamic considerations. , 2008, Therapeutic drug monitoring.
[8] BJ Parker,et al. High dose methylprednisolone therapy for the treatment of severe systemic lupus erythematosus , 2007, Lupus.
[9] W. L. Nelson,et al. ROLE OF ITRACONAZOLE METABOLITES IN CYP3A4 INHIBITION , 2004, Drug Metabolism and Disposition.
[10] J. Goldstein,et al. Identification of constitutive androstane receptor and glucocorticoid receptor binding sites in the CYP2C19 promoter. , 2003, Molecular pharmacology.
[11] N. Wood,et al. The disposition of voriconazole in mouse, rat, rabbit, guinea pig, dog, and human. , 2003, Drug metabolism and disposition: the biological fate of chemicals.
[12] D A Smith,et al. Identification of the cytochrome P450 enzymes involved in the N-oxidation of voriconazole. , 2003, Drug metabolism and disposition: the biological fate of chemicals.
[13] C. A. Kauffman,et al. Voriconazole: a new triazole antifungal agent. , 2003, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[14] Margaret M Pearson,et al. Voriconazole: A New Triazole Antifungal Agent , 2003, The Annals of pharmacotherapy.
[15] A. Feldman,et al. Plasma levels of TNF-alpha and IL-6 are inversely related to cytochrome P450-dependent drug metabolism in patients with congestive heart failure. , 2002, Journal of cardiac failure.
[16] Richard Sylvester,et al. Voriconazole versus amphotericin B for primary therapy of invasive aspergillosis. , 2002, The New England journal of medicine.
[17] N. Wood,et al. Pharmacokinetics and Safety of Voriconazole following Intravenous- to Oral-Dose Escalation Regimens , 2002, Antimicrobial Agents and Chemotherapy.
[18] S. Clarke,et al. Hepatic cytochrome P450 3A drug metabolism is reduced in cancer patients who have an acute-phase response , 2002, British Journal of Cancer.
[19] J. Pascussi,et al. Interleukin-6 negatively regulates the expression of pregnane X receptor and constitutively activated receptor in primary human hepatocytes. , 2000, Biochemical and biophysical research communications.
[20] G. Cheymol,et al. Optimisation of Itraconazole Therapy Using Target Drug Concentrations , 1998, Clinical pharmacokinetics.
[21] M. Lechner,et al. Glucocorticoid receptor-independent transcriptional induction of cytochrome P450 3A1 by metyrapone and its potentiation by glucocorticoid. , 1996, Molecular pharmacology.
[22] C. Kasper,et al. Dexamethasone responsiveness of a major glucocorticoid-inducible CYP3A gene is mediated by elements unrelated to a glucocorticoid receptor binding motif. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[23] P. Maurel,et al. Differential effects of cytokines on the inducible expression of CYP1A1, CYP1A2, and CYP3A4 in human hepatocytes in primary culture , 1995, Hepatology.
[24] S. Clissold,et al. Fluconazole. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in superficial and systemic mycoses. , 1990, Drugs.
[25] F. Frey,et al. Impact of ketoconazole on the metabolism of prednisolone , 1989, Clinical pharmacology and therapeutics.
[26] R. M. Tucker,et al. Treatment of Mycoses with Itraconazole , 1988, Annals of the New York Academy of Sciences.
[27] J. Graybill,et al. Pharmacokinetics of itraconazole following oral administration to normal volunteers , 1988, Antimicrobial Agents and Chemotherapy.
[28] B. McConkey,et al. Effects of gold, dapsone, and prednisone on serum C-reactive protein and haptoglobin and the erythrocyte sedimentation rate in rheumatoid arthritis. , 1979, Annals of the rheumatic diseases.
[29] Takahiro Yamada,et al. Rapid simultaneous determination of voriconazole and its N-oxide in human plasma using an isocratic high-performance liquid chromatography method and its clinical application. , 2012, Clinical biochemistry.
[30] H. Derendorf,et al. Pharmacokinetic/Pharmacodynamic Profile of Posaconazole , 2010, Clinical pharmacokinetics.
[31] D. Sin,et al. Effects of corticosteroids on systemic inflammation in chronic obstructive pulmonary disease. , 2005, Proceedings of the American Thoracic Society.
[32] Kathleen A. Boyle,et al. In vitro antifungal activities of voriconazole and reference agents as determined by NCCLS methods: Review of the literature , 2004, Mycopathologia.
[33] Hongbing Wang,et al. Role of Orphan Nuclear Receptors in the Regulation of Drug-Metabolising Enzymes , 2003, Clinical pharmacokinetics.