pubmed-article:15499533 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15499533 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:15499533 | lifeskim:mentions | umls-concept:C0034656 | lld:lifeskim |
pubmed-article:15499533 | lifeskim:mentions | umls-concept:C0024535 | lld:lifeskim |
pubmed-article:15499533 | lifeskim:mentions | umls-concept:C2587213 | lld:lifeskim |
pubmed-article:15499533 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:15499533 | lifeskim:mentions | umls-concept:C0039725 | lld:lifeskim |
pubmed-article:15499533 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:15499533 | pubmed:dateCreated | 2004-10-22 | lld:pubmed |
pubmed-article:15499533 | pubmed:abstractText | Dihydroartemisinin-piperaquine (DP) is a new and relatively inexpensive artemisinin-containing fixed-combination antimalarial treatment. An adult treatment course contained 6.4 mg/kg dihydroartemisinin (DHA), which is >40% lower than the level in most artemisinin-containing combinations. This raised the possibility that the efficacy of the current coformulation may not be optimal in the treatment of multidrug-resistant falciparum malaria. | lld:pubmed |
pubmed-article:15499533 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15499533 | pubmed:language | eng | lld:pubmed |
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pubmed-article:15499533 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:15499533 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:15499533 | pubmed:month | Nov | lld:pubmed |
pubmed-article:15499533 | pubmed:issn | 0022-1899 | lld:pubmed |
pubmed-article:15499533 | pubmed:author | pubmed-author:WhiteNicholas... | lld:pubmed |
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pubmed-article:15499533 | pubmed:author | pubmed-author:McGreadyRoseR | lld:pubmed |
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pubmed-article:15499533 | pubmed:author | pubmed-author:BrockmanAlanA | lld:pubmed |
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pubmed-article:15499533 | pubmed:author | pubmed-author:SrivilairitSi... | lld:pubmed |
pubmed-article:15499533 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:15499533 | pubmed:day | 15 | lld:pubmed |
pubmed-article:15499533 | pubmed:volume | 190 | lld:pubmed |
pubmed-article:15499533 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15499533 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15499533 | pubmed:pagination | 1773-82 | lld:pubmed |
pubmed-article:15499533 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:15499533 | pubmed:year | 2004 | lld:pubmed |
pubmed-article:15499533 | pubmed:articleTitle | Randomized, controlled dose-optimization studies of dihydroartemisinin-piperaquine for the treatment of uncomplicated multidrug-resistant falciparum malaria in Thailand. | lld:pubmed |
pubmed-article:15499533 | pubmed:affiliation | Shoklo Malaria Research Unit, Mae Sot, and Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand. | lld:pubmed |
pubmed-article:15499533 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:15499533 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:15499533 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:15499533 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:15499533 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:15499533 | pubmed:publicationType | Multicenter Study | lld:pubmed |
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