Cited 2 times in

Focal cerebellar infarction as an initial sign of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

DC Field Value Language
dc.contributor.author이영목-
dc.date.accessioned2019-10-28T01:33:26Z-
dc.date.available2019-10-28T01:33:26Z-
dc.date.issued2019-
dc.identifier.issn0141-8955-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/171249-
dc.description.abstractMitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a type of mitochondrial disorder and stroke-like lesions are observed prominently in the brain magnetic resonance imaging. Those stroke-like lesions of MELAS patients are usually located in the posterior quadrants and do not correspond to typical vascular territories. This case illustrates that focal cerebellar infarction can be the sole initial sign of MELAS.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherKluwer-
dc.relation.isPartOfJournal of Inherited Metabolic Disease-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleFocal cerebellar infarction as an initial sign of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pediatrics (소아청소년과학교실)-
dc.contributor.googleauthorAra Ko-
dc.contributor.googleauthorSang‐Jun Lee-
dc.contributor.googleauthorYoung‐Mock Lee-
dc.identifier.doi10.1002/jimd.12020-
dc.contributor.localIdA02955-
dc.relation.journalcodeJ01457-
dc.identifier.eissn1573-2665-
dc.identifier.pmid30693531-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1002/jimd.12020-
dc.subject.keywordMELAS-
dc.subject.keywordataxia-
dc.subject.keywordcerebellum-
dc.subject.keyworddysarthria-
dc.subject.keywordmitochondria-
dc.contributor.alternativeNameLee, Young Mock-
dc.contributor.affiliatedAuthor이영목-
dc.citation.volume42-
dc.citation.number3-
dc.citation.startPage575-
dc.citation.endPage576-
dc.identifier.bibliographicCitationJournal of Inherited Metabolic Disease, Vol.42(3) : 575-576, 2019-
dc.identifier.rimsid64199-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers

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