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dc.contributor.authorChun Ki Kim-
dc.date.accessioned2019-11-27T20:56:47Z-
dc.date.available2019-11-27T20:56:47Z-
dc.date.issued2017-07-
dc.identifier.citationCLINICAL NUCLEAR MEDICINE, v. 42, no. 7, page. 343-344en_US
dc.identifier.issn0363-9762-
dc.identifier.issn1536-0229-
dc.identifier.urihttps://insights.ovid.com/crossref?an=00003072-201707000-00033-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/115014-
dc.description.abstractAn 18F-FDG PET scan performed on a patient suspected of having early Huntington disease (HD) showed marked hypometabolism in bilateral putamen that was significantly worse than the hypometabolism in caudate. While HD could not be completely excluded, the scan finding was felt to be somewhat atypical for HD because of a lesser degree of caudate involvement. Genetic testing eventually confirmed the diagnosis of HD. This case shows that diagnosis of HD should still be considered even when putaminal hypometabolism exceeds caudate changes on 18F-FDG PET imaging.en_US
dc.language.isoen_USen_US
dc.publisherLIPPINCOTT WILLIAMS & WILKINSen_US
dc.subjectF-18-FDG PETen_US
dc.subjectHuntington diseaseen_US
dc.subjectputamenen_US
dc.titlePutaminal Hypometabolism Exceeding Caudate Abnormalities on 18F-FDG PET in Huntington Diseaseen_US
dc.typeArticleen_US
dc.relation.no7-
dc.relation.volume42-
dc.identifier.doi10.1097/RLU.0000000000001668-
dc.relation.page343-344-
dc.relation.journalCLINICAL NUCLEAR MEDICINE-
dc.contributor.googleauthorSinghal, Tarun-
dc.contributor.googleauthorKim, Chun K.-
dc.relation.code2017005954-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidchunkikim-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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