Randomized controlled trial of fosmidomycin-clindamycin versus sulfadoxine-pyrimethamine in the treatment of Plasmodium falciparum malaria
about
Chemical rescue of malaria parasites lacking an apicoplast defines organelle function in blood-stage Plasmodium falciparumInhibition of 1-Deoxy- d -Xylulose-5-Phosphate Reductoisomerase by Lipophilic Phosphonates: SAR, QSAR, and Crystallographic StudiesAntimalarial and Structural Studies of Pyridine-Containing Inhibitors of 1-Deoxyxylulose-5-phosphate ReductoisomeraseA chemical rescue screen identifies a Plasmodium falciparum apicoplast inhibitor targeting MEP isoprenoid precursor biosynthesisMalaria: an update on current chemotherapy.Comparative transcriptional analysis of homologous pathogenic and non-pathogenic Lawsonia intracellularis isolates in infected porcine cellsThe toxoplasma apicoplast phosphate translocator links cytosolic and apicoplast metabolism and is essential for parasite survival.Antimalarial compounds in Phase II clinical development.High prevalence of dhfr triple mutant and correlation with high rates of sulphadoxine-pyrimethamine treatment failures in vivo in Gabonese childrenDetermination of the active stereoisomer of the MEP pathway-targeting antimalarial agent MMV008138, and initial structure-activity studiesInadequate efficacy of a new formulation of fosmidomycin-clindamycin combination in Mozambican children less than three years old with uncomplicated Plasmodium falciparum malaria.The global pipeline of new medicines for the control and elimination of malariaExpression, characterization and inhibition of Toxoplasma gondii 1-deoxy-D-xylulose-5-phosphate reductoisomerase.Assessment of safety of the major antimalarial drugs.Update on clindamycin in the management of bacterial, fungal and protozoal infections.FR-900098, an antimalarial development candidate that inhibits the non-mevalonate isoprenoid biosynthesis pathway, shows no evidence of acute toxicity and genotoxicityDrug repositioning in the treatment of malaria and TB.Fosmidomycin as an antimalarial drug: a meta-analysis of clinical trials.Exploring inhibition of Pdx1, a component of the PLP synthase complex of the human malaria parasite Plasmodium falciparum.Treating malaria in pregnancy in developing countries: priorities in clinical research and drug development.Small molecule inhibition of apicomplexan FtsH1 disrupts plastid biogenesis in human pathogens.Phase I randomized dose-ascending placebo-controlled trials of ferroquine--a candidate anti-malarial drug--in adults with asymptomatic Plasmodium falciparum infection.In vitro activity of antifungal drugs against Plasmodium falciparum field isolates.David Roos. Interview by H. Craig Mak.Tropical medicine at the University of Tübingen.Drugs in Development for Malaria.
P2860
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P2860
Randomized controlled trial of fosmidomycin-clindamycin versus sulfadoxine-pyrimethamine in the treatment of Plasmodium falciparum malaria
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
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2007年论文
@zh-cn
name
Randomized controlled trial of ...... Plasmodium falciparum malaria
@ast
Randomized controlled trial of ...... Plasmodium falciparum malaria
@en
type
label
Randomized controlled trial of ...... Plasmodium falciparum malaria
@ast
Randomized controlled trial of ...... Plasmodium falciparum malaria
@en
prefLabel
Randomized controlled trial of ...... Plasmodium falciparum malaria
@ast
Randomized controlled trial of ...... Plasmodium falciparum malaria
@en
P2093
P2860
P50
P921
P356
P1476
Randomized controlled trial of ...... Plasmodium falciparum malaria
@en
P2093
Fortune Barondi
Jürgen F Kun
Michel A Missinou
Peter Pongratz
Sunny Oyakhirome
P2860
P304
P356
10.1128/AAC.01448-06
P407
P577
2007-02-26T00:00:00Z