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pubmed-article:19556122pubmed:abstractTextThis study was performed to assess the toxicities, the maximum-tolerated dose (MTD), the pharmacokinetics and the anti-tumour activity of gemcitabine given by 24-h hepatic arterial infusion (HAI).lld:pubmed
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pubmed-article:19556122pubmed:articleTitleA phase I and pharmacokinetic study of gemcitabine given by 24-h hepatic arterial infusion.lld:pubmed
pubmed-article:19556122pubmed:affiliationDepartment of Medical Oncology, VU University Medical Center, de Boelelaan 1117, 1081 HV Amsterdam, The Netherlands.lld:pubmed
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