pubmed-article:11304783 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11304783 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:11304783 | lifeskim:mentions | umls-concept:C0019425 | lld:lifeskim |
pubmed-article:11304783 | lifeskim:mentions | umls-concept:C0000618 | lld:lifeskim |
pubmed-article:11304783 | lifeskim:mentions | umls-concept:C0004482 | lld:lifeskim |
pubmed-article:11304783 | lifeskim:mentions | umls-concept:C0342801 | lld:lifeskim |
pubmed-article:11304783 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:11304783 | pubmed:dateCreated | 2001-4-17 | lld:pubmed |
pubmed-article:11304783 | pubmed:abstractText | To assess thiopurine S-methyltransferase (TPMT) phenotype and genotype in patients who were intolerant to treatment with mercaptopurine (MP) or azathioprine (AZA), and to evaluate their clinical management. | lld:pubmed |
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pubmed-article:11304783 | pubmed:language | eng | lld:pubmed |
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pubmed-article:11304783 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:11304783 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11304783 | pubmed:month | Apr | lld:pubmed |
pubmed-article:11304783 | pubmed:issn | 0732-183X | lld:pubmed |
pubmed-article:11304783 | pubmed:author | pubmed-author:MurrayJJ | lld:pubmed |
pubmed-article:11304783 | pubmed:author | pubmed-author:QuinnJJ | lld:pubmed |
pubmed-article:11304783 | pubmed:author | pubmed-author:EvansW EWE | lld:pubmed |
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pubmed-article:11304783 | pubmed:author | pubmed-author:KalwinskyDD | lld:pubmed |
pubmed-article:11304783 | pubmed:author | pubmed-author:RavindranathY... | lld:pubmed |
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pubmed-article:11304783 | pubmed:author | pubmed-author:RellingM VMV | lld:pubmed |
pubmed-article:11304783 | pubmed:author | pubmed-author:MargolinJJ | lld:pubmed |
pubmed-article:11304783 | pubmed:author | pubmed-author:HoldsworthMM | lld:pubmed |
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pubmed-article:11304783 | pubmed:author | pubmed-author:SteuberCC | lld:pubmed |
pubmed-article:11304783 | pubmed:author | pubmed-author:HonY YYY | lld:pubmed |
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pubmed-article:11304783 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11304783 | pubmed:day | 15 | lld:pubmed |
pubmed-article:11304783 | pubmed:volume | 19 | lld:pubmed |
pubmed-article:11304783 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11304783 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11304783 | pubmed:pagination | 2293-301 | lld:pubmed |
pubmed-article:11304783 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:11304783 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11304783 | pubmed:articleTitle | Preponderance of thiopurine S-methyltransferase deficiency and heterozygosity among patients intolerant to mercaptopurine or azathioprine. | lld:pubmed |
pubmed-article:11304783 | pubmed:affiliation | St Jude Children's Research Hospital and University of Tennessee, Memphis 38101-0318, USA. william.evans@stjude.org | lld:pubmed |
pubmed-article:11304783 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11304783 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:11304783 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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