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Kurt Schaecher

Researcher at Medical Corps

Publications -  10
Citations -  1995

Kurt Schaecher is an academic researcher from Medical Corps. The author has contributed to research in topics: Plasmodium falciparum & Malaria. The author has an hindex of 8, co-authored 10 publications receiving 1832 citations. Previous affiliations of Kurt Schaecher include United States Department of the Army.

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Evidence of Artemisinin-Resistant Malaria in Western Cambodia

TL;DR: Artemisinins are potent and rapidly acting antimalarial drugs, and their widespread use for treating patients with Plasmodium falciparum malaria raises the question of emerging drug resistance.
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Artemisinin Resistance in Cambodia: A Clinical Trial Designed to Address an Emerging Problem in Southeast Asia

TL;DR: Artemisinin resistance has emerged along the Thai-Cambodian border and the potentially devastating implications of spreading resistance to a drug that currently has no successor call for further studies of this emerging problem.
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Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial

TL;DR: There is no pharmacodynamic benefit of increasing the daily dose of AS (4mg/kg) currently recommended for short-course combination treatment of uncomplicated malaria, even in regions with emerging artemisinin resistance, as long as the partner drug retains high efficacy.
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Polymorphism patterns in Duffy-binding protein among Thai Plasmodium vivax isolates

TL;DR: Polymorphisms within PvDBPII indicated that Thai vivax malaria parasites are genetically diverse and the difference between the rates of nonsynonymous and synonymous mutations estimated by the Nei and Gojobori's method suggested that Pv DBPII antigen appears to be under selective pressure.
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Plasmodium falciparum gametocyte carriage is associated with subsequent Plasmodium vivax relapse after treatment.

TL;DR: The findings suggest that the majority of vivax infections arising after treatment of falciparum malaria originate from relapsing liver-stage parasites, which may benefit from empiric treatment with an 8-aminoquinolone such as primaquine.