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dc.contributor.authorFreeman, Jane
dc.contributor.authorBaines, Simon D.
dc.contributor.authorJabes, Daniela
dc.contributor.authorWilcox, Mark H.
dc.date.accessioned2013-08-22T11:45:02Z
dc.date.available2013-08-22T11:45:02Z
dc.date.issued2005-09
dc.identifier.citationFreeman , J , Baines , S D , Jabes , D & Wilcox , M H 2005 , ' Comparison of the efficacy of ramoplanin and vancomycin in both in vitro and in vivo models of clindamycin-induced Clostridium difficile infection ' , Journal of Antimicrobial Chemotherapy , vol. 56 , no. 4 , pp. 717-25 . https://doi.org/10.1093/jac/dki321
dc.identifier.issn0305-7453
dc.identifier.urihttp://hdl.handle.net/2299/11442
dc.description.abstractTreatment of Clostridium difficile infection (CDI) is limited primarily to either metronidazole or vancomycin. We compared vancomycin and a novel glycolipodepsipeptide, ramoplanin, in both hamster and in vitro gut models of clindamycin-induced CDI.en
dc.format.extent9
dc.format.extent249108
dc.language.isoeng
dc.relation.ispartofJournal of Antimicrobial Chemotherapy
dc.titleComparison of the efficacy of ramoplanin and vancomycin in both in vitro and in vivo models of clindamycin-induced Clostridium difficile infectionen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionMicrobiology and Biotechnology
dc.contributor.institutionBiosciences Research Group
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionCentre for Future Societies Research
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1093/jac/dki321
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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