https://scholars.lib.ntu.edu.tw/handle/123456789/198048
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor | 神經科 | en |
dc.contributor.author | HSU, Y-S | en |
dc.contributor.author | CHANG, YANG-CHYUAN | en |
dc.contributor.author | LEE, WANG-TSO | en |
dc.contributor.author | NI, YEN-HSUAN | en |
dc.contributor.author | HSU, HONG-YUAN | en |
dc.contributor.author | CHANG, MEI-HWEI | en |
dc.creator | 徐玉山;張楊全;李旺祚;倪衍玄;許宏遠;張美惠 | zh-tw |
dc.creator | HSU, Y-S;CHANG, YANG-CHYUAN;LEE, WANG-TSO;NI, YEN-HSUAN;HSU, HONG-YUAN;CHANG, MEI-HWEI | en |
dc.date | 2003 | en |
dc.date.accessioned | 2009-01-19T03:57:58Z | - |
dc.date.accessioned | 2018-07-12T01:42:31Z | - |
dc.date.available | 2009-01-19T03:57:58Z | - |
dc.date.available | 2018-07-12T01:42:31Z | - |
dc.date.issued | 2003 | - |
dc.identifier.uri | http://ntur.lib.ntu.edu.tw//handle/246246/99668 | - |
dc.description.abstract | We studied the sensory evoked potentials in pediatric Wilson disease to verify their subclinical neurologic involvement and to elucidate the role of cirrhosis in abnormal evoked potentials in non-neurologic Wilson disease. Thirty children (17 male, 13 female), diagnosed with Wilson disease before 18 years, were enrolled. The mean age during studies was 15 . 8 +/- 6.3 years, and disease duration since diagnosis was 3 . 0 +/- 3.3 years. In 12 neurologic Wilson disease cases, there were prolonged interpeak latencies of brainstem auditory evoked potentials III-V, IN, somatosensory evoked potentials N13-N20 (P < 0.01 vs controls and non- neurologic cases), and P100 latency (P < 0.01 vs controls). All 12 patients had at least one abnormal evoked potential, including 91.7% brainstem auditory, 58.3% somatosensory, and 25% visual evoked potentials. In 18 non-neurologic Wilson disease cases, there were still prolonged interpeak latencies for brainstem auditory evoked potentials IN and somatosensory evoked potentials N13-N20 (P < 0.05 vs controls), with 27.8% of them having at least one abnormal evoked potential, including 16.6% brainstem auditory, 5.6% somatosensory, and 11.1% visual evoked potentials . In those with non-neurologic Wilson disease, there were no significant differences in all the evoked potential parameters between the cirrhotic and non-cirrhotic patients. (C) 2003 by Elsevier Inc. All rights reserved. | en |
dc.language | en-us | en |
dc.language.iso | en_US | - |
dc.relation | PEDIATRIC NEUROLOGY v.29 n.1 pp.42-45 | en |
dc.relation.ispartof | PEDIATRIC NEUROLOGY | - |
dc.subject | DEGENERATION | en |
dc.title | The Diagnostic Value of Sensory Evoked Potentials in Pediatric Wilson Disease | en |
dc.relation.pages | 42-45 | - |
dc.relation.journalvolume | v.29 | - |
dc.relation.journalissue | n.1 | - |
item.languageiso639-1 | en_US | - |
item.grantfulltext | none | - |
item.fulltext | no fulltext | - |
顯示於: | 醫學系 |
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