| pubmed-article:9586893 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C0442027 | lld:lifeskim |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C0006948 | lld:lifeskim |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C0671970 | lld:lifeskim |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C0439611 | lld:lifeskim |
| pubmed-article:9586893 | lifeskim:mentions | umls-concept:C0596581 | lld:lifeskim |
| pubmed-article:9586893 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:9586893 | pubmed:dateCreated | 1998-6-4 | lld:pubmed |
| pubmed-article:9586893 | pubmed:abstractText | To evaluate the toxicology and pharmacology of an orally active fluoropyrimidine given as a continuous daily dose divided into two portions for 6 weeks, and to determine the maximal-tolerated daily dose (MTD) and the suggested phase II daily dose. | lld:pubmed |
| pubmed-article:9586893 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9586893 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9586893 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9586893 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9586893 | pubmed:month | May | lld:pubmed |
| pubmed-article:9586893 | pubmed:issn | 0732-183X | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:CreavenP JPJ | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:BudmanD RDR | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:GriffinTT | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:CARRB WBW | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:OsterwalderBB | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:GordonR JRJ | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:ReignerBB | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:MeropolN JNJ | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:LichtmanS MSM | lld:pubmed |
| pubmed-article:9586893 | pubmed:author | pubmed-author:BerghornEE | lld:pubmed |
| pubmed-article:9586893 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9586893 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:9586893 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9586893 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9586893 | pubmed:pagination | 1795-802 | lld:pubmed |
| pubmed-article:9586893 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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| pubmed-article:9586893 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9586893 | pubmed:articleTitle | Preliminary studies of a novel oral fluoropyrimidine carbamate: capecitabine. | lld:pubmed |
| pubmed-article:9586893 | pubmed:affiliation | Department of Medicine, North Shore University Hospital, New York University Medical College, Manhasset 11030, USA. budman@nshs.edu | lld:pubmed |
| pubmed-article:9586893 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9586893 | pubmed:publicationType | Clinical Trial | lld:pubmed |
| pubmed-article:9586893 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:9586893 | pubmed:publicationType | Multicenter Study | lld:pubmed |
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