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Clinical Experience with Topiramate in Korean Patients with Epilepsy

DC Field Value Language
dc.contributor.authorCho, YW-
dc.contributor.authorYi, SD-
dc.contributor.authorKim, JH-
dc.contributor.authorJung, Ki-Young-
dc.contributor.authorShon, YM-
dc.contributor.authorShin, WC-
dc.contributor.authorSeo, DW-
dc.contributor.authorHwang, H-
dc.creator정기영-
dc.date.accessioned2014-07-24T08:36:01Z-
dc.date.available2014-07-24T08:36:01Z-
dc.date.issued2010-06-
dc.identifier.citationEpilepsia, Vol.51 Suppl.4, pp. 75-76-
dc.identifier.issn0013-9580-
dc.identifier.urihttps://hdl.handle.net/10371/92639-
dc.description.abstractPurpose: This study aims to evaluate the clinical experiences, including
efficacy and adverse events, of topiramate in Korea during the past
10 years.
Method: This was an open-label, retrospective observation with post
marketing surveillance data of topiramate. 4535 epilepsy patients were
enrolled in this study. The subjects were only included from epileptologists
whose data included studies of at least a 16-weeks duration period.
The survey contained various issues, such as efficacy (responder
rate, seizure-free rate), safety, adverse effects and the quality of life in
patients.
-
dc.language.isoenen
dc.publisherWileyen
dc.subject의약학en
dc.titleClinical Experience with Topiramate in Korean Patients with Epilepsyen
dc.typeArticle-
dc.identifier.doi10.1111/j.1528-1167.2010.02658.x-
dc.description.srndOAIID:oai:osos.snu.ac.kr:snu2010-01/102/2014017262/3-
dc.description.srndSEQ:3-
dc.description.srndPERF_CD:SNU2010-01-
dc.description.srndEVAL_ITEM_CD:102-
dc.description.srndUSER_ID:2014017262-
dc.description.srndADJUST_YN:Y-
dc.description.srndEMP_ID:A079623-
dc.description.srndDEPT_CD:801-
dc.description.srndCITE_RATE:3.955-
dc.description.srndDEPT_NM:의학과-
dc.description.srndSCOPUS_YN:Y-
dc.description.srndCONFIRM:Y-
dc.identifier.srnd2010-01/102/2014017262/3-
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