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dc.contributor.authorBayrak A.O.
dc.contributor.authorTürker H.
dc.contributor.authorYilmaz A.
dc.contributor.authorOnar M.K.
dc.date.accessioned2020-06-21T09:24:59Z
dc.date.available2020-06-21T09:24:59Z
dc.date.issued2007
dc.identifier.issn1019-1941
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3905
dc.description.abstractPatients with hereditary neuropathy at high risk of severe vincristine neurotoxicity are well known. Here, along with a review of the literature, we described two patients with unrecognized hereditary neuropathy who developed foot drop following low dose vincristine therapy. With this report, we wanted to emphasize the importance of detailed neurologic examination and history taking before initiating therapy.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHereditary neuropathyen_US
dc.subjectNeurotoxicityen_US
dc.subjectVincristinen_US
dc.titleSevere peripheral neuropathy secondary to vincristine therapyen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume20en_US
dc.identifier.issue2en_US
dc.identifier.startpage122en_US
dc.identifier.endpage126en_US
dc.relation.journalMarmara Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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