Pharmacokinetic mismatch does not lead to emergence of isoniazid- or rifampin-resistant Mycobacterium tuberculosis but to better antimicrobial effect: a new paradigm for antituberculosis drug scheduling.
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Concentration-Dependent Antagonism and Culture Conversion in Pulmonary Tuberculosis.Impact of nonlinear interactions of pharmacokinetics and MICs on sputum bacillary kill rates as a marker of sterilizing effect in tuberculosis.Ethambutol pharmacokinetic variability is linked to body mass in overweight, obese, and extremely obese people.Outwitting evolution: fighting drug-resistant TB, malaria, and HIV.TB and HIV Therapeutics: Pharmacology Research Priorities.Meta-analysis of clinical studies supports the pharmacokinetic variability hypothesis for acquired drug resistance and failure of antituberculosis therapy.Poor Penetration of Antibiotics Into Pericardium in Pericardial Tuberculosis.A Long-term Co-perfused Disseminated Tuberculosis-3D Liver Hollow Fiber Model for Both Drug Efficacy and Hepatotoxicity in BabiesAmikacin Optimal Exposure Targets in the Hollow-Fiber System Model of TuberculosisDrug Concentration Thresholds Predictive of Therapy Failure and Death in Children With Tuberculosis: Bread Crumb Trails in Random Forests.Concentration-Dependent Synergy and Antagonism of Linezolid and Moxifloxacin in the Treatment of Childhood Tuberculosis: The Dynamic Duo.Partnerships to Design Novel Regimens to Treat Childhood Tuberculosis, Sui Generis: The Road Ahead.Rifampicin mono-resistant tuberculosis in France: a 2005-2010 retrospective cohort analysis.Pharmacologic considerations in use and development of antituberculosis drugs.Nonclinical models for antituberculosis drug development: a landscape analysis.Forecasting Accuracy of the Hollow Fiber Model of Tuberculosis for Clinical Therapeutic Outcomes.Linezolid Dose That Maximizes Sterilizing Effect While Minimizing Toxicity and Resistance Emergence for Tuberculosis.Systematic Analysis of Hollow Fiber Model of Tuberculosis Experiments.A programme to create short-course chemotherapy for pulmonary Mycobacterium avium disease based on pharmacokinetics/pharmacodynamics and mathematical forecasting.Pharmacokinetic mismatch of tuberculosis drugs.Reply to “Pharmacokinetic Mismatch of Tuberculosis Drugs”.Pharmacokinetics and pharmacogenetics of anti-tubercular drugs: a tool for treatment optimization?Translational Modeling of Antibacterial Agents
P2860
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P2860
Pharmacokinetic mismatch does not lead to emergence of isoniazid- or rifampin-resistant Mycobacterium tuberculosis but to better antimicrobial effect: a new paradigm for antituberculosis drug scheduling.
description
2011 nî lūn-bûn
@nan
2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Pharmacokinetic mismatch does ...... ituberculosis drug scheduling.
@ast
Pharmacokinetic mismatch does ...... ituberculosis drug scheduling.
@en
type
label
Pharmacokinetic mismatch does ...... ituberculosis drug scheduling.
@ast
Pharmacokinetic mismatch does ...... ituberculosis drug scheduling.
@en
prefLabel
Pharmacokinetic mismatch does ...... ituberculosis drug scheduling.
@ast
Pharmacokinetic mismatch does ...... ituberculosis drug scheduling.
@en
P2093
P2860
P356
P1476
Pharmacokinetic mismatch does ...... ituberculosis drug scheduling.
@en
P2093
Carleton Sherman
Claudia Meek
Richard Leff
P2860
P304
P356
10.1128/AAC.00269-11
P407
P577
2011-09-06T00:00:00Z