Population pharmacokinetics and pharmacodynamics of artemether and lumefantrine during combination treatment in children with uncomplicated falciparum malaria in Tanzania.
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Artemether-lumefantrine treatment of uncomplicated Plasmodium falciparum malaria: a systematic review and meta-analysis of day 7 lumefantrine concentrations and therapeutic response using individual patient dataPharmacokinetic and pharmacodynamic considerations in antimalarial dose optimizationMaking the most of clinical data: reviewing the role of pharmacokinetic-pharmacodynamic models of anti-malarial drugsAlternatively spliced transcripts and novel pseudogenes of the Plasmodium falciparum resistance-associated locus pfcrt detected in East African malaria patientsBaseline data of parasite clearance in patients with falciparum malaria treated with an artemisinin derivative: an individual patient data meta-analysis.Optimizing the programmatic deployment of the anti-malarials artemether-lumefantrine and dihydroartemisinin-piperaquine using pharmacological modelling.Modelling the time course of antimalarial parasite killing: a tour of animal and human models, translation and challengesPharmacokinetic and pharmacodynamic characteristics of a new pediatric formulation of artemether-lumefantrine in African children with uncomplicated Plasmodium falciparum malariaPopulation pharmacokinetics of artemether, lumefantrine, and their respective metabolites in Papua New Guinean children with uncomplicated malaria.Pharmacokinetics of a novel sublingual spray formulation of the antimalarial drug artemether in African children with malaria.Pharmacokinetics of a novel sublingual spray formulation of the antimalarial drug artemether in healthy adults.Plasmodium falciparum population dynamics during the early phase of anti-malarial drug treatment in Tanzanian children with acute uncomplicated malaria.Rethinking Dosing Regimen Selection of Piperaquine for Malaria Chemoprevention: A Simulation Study.How Robust Are Malaria Parasite Clearance Rates as Indicators of Drug Effectiveness and Resistance?Optimal designs for population pharmacokinetic studies of the partner drugs co-administered with artemisinin derivatives in patients with uncomplicated falciparum malariaPharmacokinetics and pharmacodynamics of oral artesunate monotherapy in patients with uncomplicated Plasmodium falciparum malaria in western Cambodia.Population pharmacokinetics of Artemether and dihydroartemisinin in pregnant women with uncomplicated Plasmodium falciparum malaria in UgandaMRP2/ABCC2 C1515Y polymorphism modulates exposure to lumefantrine during artemether-lumefantrine antimalarial therapy.Plasmodium falciparum drug resistance phenotype as assessed by patient antimalarial drug levels and its association with pfmdr1 polymorphismsA multistate tuberculosis pharmacometric model: a framework for studying anti-tubercular drug effects in vitro.Incorporating Stage-Specific Drug Action into Pharmacological Modeling of Antimalarial Drug TreatmentApplication of the Multistate Tuberculosis Pharmacometric Model in Patients With Rifampicin-Treated Pulmonary TuberculosisPopulation pharmacokinetics of mefloquine, piperaquine and artemether-lumefantrine in Cambodian and Tanzanian malaria patients.Population Pharmacokinetics and Pharmacodynamics of Lumefantrine in Young Ugandan Children Treated With Artemether-Lumefantrine for Uncomplicated Malaria.Pharmacokinetic profile of artemisinin derivatives and companion drugs used in artemisinin-based combination therapies for the treatment of Plasmodium falciparum malaria in children.Oil-Fortified Maize Porridge Increases Absorption of Lumefantrine in Children with Uncomplicated Falciparum Malaria.Comparable lumefantrine oral bioavailability when co-administered with oil-fortified maize porridge or milk in healthy volunteers.Teratogenicity of Artemether-Clindamycin Nanostructured Lipid Carriers in Rats.Assessing the impact of imperfect adherence to artemether-lumefantrine on malaria treatment outcomes using within-host modelling.Pharmacokinetic considerations for use of artemisinin-based combination therapies against falciparum malaria in different ethnic populations.Artemether-lumefantrine dosing for malaria treatment in young children and pregnant women: A pharmacokinetic-pharmacodynamic meta-analysis.Population pharmacokinetics of artemether, dihydroartemisinin and lumefantrine in Rwandese pregnant women treated for uncomplicated malaria
P2860
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P2860
Population pharmacokinetics and pharmacodynamics of artemether and lumefantrine during combination treatment in children with uncomplicated falciparum malaria in Tanzania.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@ast
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@en
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@nl
type
label
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@ast
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@en
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@nl
prefLabel
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@ast
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@en
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@nl
P2093
P2860
P921
P356
P1476
Population pharmacokinetics an ...... alciparum malaria in Tanzania.
@en
P2093
Andreas Mårtensson
Anna Annerberg
Billy Ngasala
Michael Ashton
Niklas Lindegårdh
Sabina Dahlström
Sofia Friberg Hietala
Zul Premji
P2860
P304
P356
10.1128/AAC.00252-10
P407
P577
2010-08-16T00:00:00Z