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| pubmed-article:19646280 | lifeskim:mentions | umls-concept:C0008976 | lld:lifeskim |
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| pubmed-article:19646280 | lifeskim:mentions | umls-concept:C1704675 | lld:lifeskim |
| pubmed-article:19646280 | lifeskim:mentions | umls-concept:C0574032 | lld:lifeskim |
| pubmed-article:19646280 | lifeskim:mentions | umls-concept:C0205390 | lld:lifeskim |
| pubmed-article:19646280 | lifeskim:mentions | umls-concept:C0205464 | lld:lifeskim |
| pubmed-article:19646280 | lifeskim:mentions | umls-concept:C0694643 | lld:lifeskim |
| pubmed-article:19646280 | pubmed:dateCreated | 2009-8-24 | lld:pubmed |
| pubmed-article:19646280 | pubmed:abstractText | The selective MAO-B inhibitor selegiline has been evaluated in clinical trials as a potential medication for the treatment of cocaine dependence. This study evaluated the safety of and pharmacologic interactions between 7 days of transdermal selegiline dosed with patches (Selegiline Transdermal System, STS) that deliver 6 mg/24 hours and 2.5 mg/kg of cocaine administered over 4 hours. | lld:pubmed |
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| pubmed-article:19646280 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:19646280 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19646280 | pubmed:issn | 1472-6904 | lld:pubmed |
| pubmed-article:19646280 | pubmed:author | pubmed-author:JacobPeytonP3... | lld:pubmed |
| pubmed-article:19646280 | pubmed:author | pubmed-author:LinEmilE | lld:pubmed |
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| pubmed-article:19646280 | pubmed:author | pubmed-author:MendelsonJohn... | lld:pubmed |
| pubmed-article:19646280 | pubmed:author | pubmed-author:EverhartThoma... | lld:pubmed |
| pubmed-article:19646280 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19646280 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:19646280 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19646280 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19646280 | pubmed:pagination | 13 | lld:pubmed |
| pubmed-article:19646280 | pubmed:dateRevised | 2010-9-27 | lld:pubmed |
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