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Semantic variant primary progressive aphasia with a pathogenic variant p.Asp40Gly in the ANXA11 gene

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dc.contributor.authorKim, EJ-
dc.contributor.authorMoon, SY-
dc.contributor.authorKim, HJ-
dc.contributor.authorJung, NY-
dc.contributor.authorLee, SM-
dc.contributor.authorKim, YE-
dc.date.accessioned2023-03-24T06:27:04Z-
dc.date.available2023-03-24T06:27:04Z-
dc.date.issued2022-
dc.identifier.issn1351-5101-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/25129-
dc.description.abstractWe report a patient with right-predominant semantic variant primary progressive aphsia linked with p.Asp40Gly variant of ANXA11, which is the first description of frontotemporal dementia without clinical and electrophysiological evidences of amyotrophic lateral sclerosis associated with a known pathogenic variant of ANXA11.-
dc.language.isoen-
dc.subject.MESHAmyotrophic Lateral Sclerosis-
dc.subject.MESHAphasia, Primary Progressive-
dc.subject.MESHFrontotemporal Dementia-
dc.subject.MESHHumans-
dc.subject.MESHSemantics-
dc.titleSemantic variant primary progressive aphasia with a pathogenic variant p.Asp40Gly in the ANXA11 gene-
dc.typeArticle-
dc.identifier.pmid36073198-
dc.subject.keywordamyotrophic lateral sclerosis-
dc.subject.keywordANXA11-
dc.subject.keywordfrontotemporal dementia-
dc.subject.keywordsemantic variant primary progressive aphasia-
dc.contributor.affiliatedAuthorMoon, SY-
dc.type.localJournal Papers-
dc.identifier.doi10.1111/ene.15455-
dc.citation.titleEuropean journal of neurology-
dc.citation.volume29-
dc.citation.number10-
dc.citation.date2022-
dc.citation.startPage3124-
dc.citation.endPage3126-
dc.identifier.bibliographicCitationEuropean journal of neurology, 29(10). : 3124-3126, 2022-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.identifier.eissn1468-1331-
dc.relation.journalidJ013515101-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Neurology
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