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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, Eun-Joo-
dc.contributor.authorMoon, So Young-
dc.contributor.authorKim, Hee-Jin-
dc.contributor.authorJung, Na-Yeon-
dc.contributor.authorLee, Sun Min-
dc.contributor.authorKim, Young Eun-
dc.date.accessioned2022-10-25T06:57:20Z-
dc.date.available2022-10-25T06:57:20Z-
dc.date.created2022-10-06-
dc.date.issued2022-10-
dc.identifier.issn1351-5101-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/172530-
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.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.titleSemantic variant primary progressive aphasia with a pathogenic variant p.Asp40Gly in the ANXA11 gene-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Young Eun-
dc.identifier.doi10.1111/ene.15455-
dc.identifier.scopusid2-s2.0-85137533223-
dc.identifier.wosid000852485600029-
dc.identifier.bibliographicCitationEUROPEAN JOURNAL OF NEUROLOGY, v.29, no.10, pp.3124 - 3126-
dc.relation.isPartOfEUROPEAN JOURNAL OF NEUROLOGY-
dc.citation.titleEUROPEAN JOURNAL OF NEUROLOGY-
dc.citation.volume29-
dc.citation.number10-
dc.citation.startPage3124-
dc.citation.endPage3126-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusannexin-
dc.subject.keywordPlusannexin a11-
dc.subject.keywordPlusfluorodeoxyglucose f 18-
dc.subject.keywordPluspasp 40gly-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusaged-
dc.subject.keywordPlusanamnesis-
dc.subject.keywordPlusArticle-
dc.subject.keywordPlusbehavior assessment-
dc.subject.keywordPlusbrain-
dc.subject.keywordPlusbrain atrophy-
dc.subject.keywordPluscase report-
dc.subject.keywordPlusclinical article-
dc.subject.keywordPlusclinical feature-
dc.subject.keywordPlusdaily life activity-
dc.subject.keywordPlusdisease severity-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusfollow up-
dc.subject.keywordPlusgene mutation-
dc.subject.keywordPlusgenetic screening-
dc.subject.keywordPlusgenetic variability-
dc.subject.keywordPlusglucose metabolism-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusneuroimaging-
dc.subject.keywordPlusneuropsychiatric inventory-
dc.subject.keywordPlusneuropsychological test-
dc.subject.keywordPluspositron emission tomography-
dc.subject.keywordPlusprimary progressive aphasia-
dc.subject.keywordPlussemantic variant primary progressive aphasia-
dc.subject.keywordPlusshort term memory-
dc.subject.keywordPlusT1 weighted imaging-
dc.subject.keywordPlusT2 weighted imaging-
dc.subject.keywordPlustemporal lobe-
dc.subject.keywordPlusverbal learning-
dc.subject.keywordPluswhole exome sequencing-
dc.subject.keywordPlusword recognition-
dc.subject.keywordPlusamyotrophic lateral sclerosis-
dc.subject.keywordPlusdiagnostic imaging-
dc.subject.keywordPlusfrontotemporal dementia-
dc.subject.keywordPlusgenetics-
dc.subject.keywordPlusprimary progressive aphasia-
dc.subject.keywordPlussemantics-
dc.subject.keywordAuthorANXA11-
dc.subject.keywordAuthoramyotrophic lateral sclerosis-
dc.subject.keywordAuthorfrontotemporal dementia-
dc.subject.keywordAuthorsemantic variant primary progressive aphasia-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/ene.15455-
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