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Gelsolin variant amyloidosis mimicking progressive bulbar palsy

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dc.contributor.authorPark, Jinseok-
dc.contributor.authorKim, Young-Eun-
dc.contributor.authorOh, Ki-Wook-
dc.contributor.authorNahm, Minyeop-
dc.contributor.authorKim, Yu Jeong-
dc.contributor.authorKim, Mi Jung-
dc.contributor.authorKim, Seung Hyun-
dc.date.accessioned2023-07-05T02:43:50Z-
dc.date.available2023-07-05T02:43:50Z-
dc.date.created2022-10-06-
dc.date.issued2022-08-
dc.identifier.issn0148-639X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/186128-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.titleGelsolin variant amyloidosis mimicking progressive bulbar palsy-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Jinseok-
dc.contributor.affiliatedAuthorKim, Young-Eun-
dc.contributor.affiliatedAuthorOh, Ki-Wook-
dc.contributor.affiliatedAuthorKim, Mi Jung-
dc.contributor.affiliatedAuthorKim, Seung Hyun-
dc.identifier.doi10.1002/mus.27714-
dc.identifier.scopusid2-s2.0-85138399642-
dc.identifier.wosid000855894200001-
dc.identifier.bibliographicCitationMUSCLE & NERVE, v.66, no.5, pp.E28 - E33-
dc.relation.isPartOfMUSCLE & NERVE-
dc.citation.titleMUSCLE & NERVE-
dc.citation.volume66-
dc.citation.number5-
dc.citation.startPageE28-
dc.citation.endPageE33-
dc.type.rimsART-
dc.type.docTypeLetter; Early Access-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusgelsolin-
dc.subject.keywordPlusgelsolin-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusamyloidosis-
dc.subject.keywordPlusatrophy-
dc.subject.keywordPlusautosomal dominant inheritance-
dc.subject.keywordPlusbrother-
dc.subject.keywordPlusbulbar paralysis-
dc.subject.keywordPluscase report-
dc.subject.keywordPlusclinical article-
dc.subject.keywordPlusdiagnostic error-
dc.subject.keywordPlusdry eye syndrome-
dc.subject.keywordPlusdysarthria-
dc.subject.keywordPlusdysphagia-
dc.subject.keywordPlusface muscle-
dc.subject.keywordPlusfacial nerve paralysis-
dc.subject.keywordPlusfacial weakness-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusgenetic screening-
dc.subject.keywordPlusgenetic variability-
dc.subject.keywordPlusgrandmother-
dc.subject.keywordPlushereditary gelsolin amyloidosis-
dc.subject.keywordPlushuman-
dc.subject.keywordPluslattice corneal dystrophy-
dc.subject.keywordPlusLetter-
dc.subject.keywordPlusmasseter muscle-
dc.subject.keywordPlusmiddle aged-
dc.subject.keywordPlusmother-
dc.subject.keywordPlusmotor neuron disease-
dc.subject.keywordPlusmuscle action potential-
dc.subject.keywordPlusmuscle twitch-
dc.subject.keywordPlusmyokymia-
dc.subject.keywordPlusneedle electromyography-
dc.subject.keywordPlusnerve regeneration-
dc.subject.keywordPlusneuroimaging-
dc.subject.keywordPlusneurologic examination-
dc.subject.keywordPlusnuclear magnetic resonance imaging-
dc.subject.keywordPlusophthalmologist-
dc.subject.keywordPlusorbicularis oris muscle-
dc.subject.keywordPlusptosis (eyelid)-
dc.subject.keywordPlusskin turgor-
dc.subject.keywordPlusslit lamp microscopy-
dc.subject.keywordPlusslurred speech-
dc.subject.keywordPlustongue atrophy-
dc.subject.keywordPlusweakness-
dc.subject.keywordPluswhole exome sequencing-
dc.subject.keywordPlusfamilial amyloid polyneuropathy-
dc.subject.keywordPlusfamilial amyloidosis-
dc.subject.keywordPlusgenetics-
dc.subject.keywordPlusmutation-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/mus.27714-
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서울 의과대학 > 서울 재활의학교실 > 1. Journal Articles
서울 의과대학 > 서울 진단검사의학교실 > 1. Journal Articles
서울 의과대학 > 서울 신경과학교실 > 1. Journal Articles
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