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자기공명영상에서 전형적인 이상 소견을 보인 소아마비양 증후군 환자 1예 : (A Case of Poliomyelitis-like Syndrome with Typical Abnormalities in MRI)

DC Field Value Language
dc.contributor.author김석일-
dc.contributor.author구자성-
dc.contributor.author윤두상-
dc.contributor.author김병건-
dc.contributor.author배희준-
dc.date.accessioned2024-08-08T01:51:41Z-
dc.date.available2024-08-08T01:51:41Z-
dc.date.created2024-08-07-
dc.date.created2024-08-07-
dc.date.issued2002-
dc.identifier.citationAnnals of Clinical Neurophysiology, Vol.4 No.1, pp.56-59-
dc.identifier.issn2508-691X-
dc.identifier.urihttps://hdl.handle.net/10371/208752-
dc.description.abstractA 28-year-old man presented with headache, fever, and myalgia. Subsequently, rapidly progressive quadriplegia with areflexia developed. CSF examination revealed moderate pleocytosis and protein elevation. MRI of brain and spinal cord showed hyperintense lesions on T2-weighted image at midbrain and ventral horns along the whole spinal cord. Serial serologic examinations of CSF for Epstein-Barr virus and cytomegalovirus were negative. Culture and neutralization tests of stool and CSF for enterovirus were negative. Although the etiologic pathogen was not identified, we diagnosed him as poliomyelitis-like syndrome by clinical features and findings of MRI.-
dc.language한국어-
dc.publisher대한임상신경생리학회-
dc.title자기공명영상에서 전형적인 이상 소견을 보인 소아마비양 증후군 환자 1예-
dc.title.alternative(A Case of Poliomyelitis-like Syndrome with Typical Abnormalities in MRI)-
dc.typeArticle-
dc.citation.journaltitleAnnals of Clinical Neurophysiology-
dc.citation.endpage59-
dc.citation.number1-
dc.citation.startpage56-
dc.citation.volume4-
dc.identifier.kciidART001327257-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthor배희준-
dc.description.journalClass2-
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  • College of Medicine
  • Department of Medicine
Research Area 뇌경색, 뇌졸중, 혈관성 인지장애 및 치매

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