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PATTERN DIFFERENCE OF DISSOCIATED HAND MUSCLE ATROPHY IN AMYOTROPHIC LATERAL SCLEROSIS AND VARIANTS

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dc.contributor.authorKim, Jee-Eun-
dc.contributor.authorHong, Yoon-Ho-
dc.contributor.authorLee, Joon-Hyung-
dc.contributor.authorAhn, Suk-Won-
dc.contributor.authorKim, Sung-Min-
dc.contributor.authorPark, Kyung-Seok-
dc.contributor.authorSung, Jung-Joon-
dc.contributor.authorLee, Kwang-Woo-
dc.contributor.authorSeong, Seung-Yong-
dc.date.available2019-03-08T17:56:24Z-
dc.date.issued2015-03-
dc.identifier.issn0148-639X-
dc.identifier.issn1097-4598-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/9790-
dc.description.abstractIntroduction: Split hand is considered to be a specific feature of amyotrophic lateral sclerosis (ALS). Methods: We evaluated the pattern difference of intrinsic hand muscles of upper limb-onset ALS (UL-ALS), upper limb-onset progressive muscular atrophy (UL-PMA), brachial amyotrophic diplegia (BAD), and Hirayama disease (HD) by measuring objective electrophysiological markers. Results: The abductor digiti minimi (ADM)/abductor pollicis brevis (APB) compound muscle action potential (CMAP) amplitude ratio was significantly higher in UL-ALS than other variants, but a considerable proportion of UL-ALS cases had an amplitude ratio in the range of other variants. Absent APB CMAP and abnormally high ADM/APB CMAP amplitude ratio (4) occurred only with UL-ALS. Conversely, an absent ADM CMAP was identified only in UL-PMA and BAD. Conclusions: The absolute ADM/APB CMAP amplitude ratio was not specific for ALS; however, several findings from simple electrophysiological measurements may help predict prognosis in patients with motor neuron diseases and may be early diagnostic markers for ALS. Muscle Nerve 51: 333-337, 2015-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-
dc.titlePATTERN DIFFERENCE OF DISSOCIATED HAND MUSCLE ATROPHY IN AMYOTROPHIC LATERAL SCLEROSIS AND VARIANTS-
dc.typeArticle-
dc.identifier.doi10.1002/mus.24323-
dc.identifier.bibliographicCitationMUSCLE & NERVE, v.51, no.3, pp 333 - 337-
dc.description.isOpenAccessN-
dc.identifier.wosid000349677300004-
dc.identifier.scopusid2-s2.0-84923057841-
dc.citation.endPage337-
dc.citation.number3-
dc.citation.startPage333-
dc.citation.titleMUSCLE & NERVE-
dc.citation.volume51-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthoramyotrophic lateral sclerosis-
dc.subject.keywordAuthorbrachial amyotrophic diplegia-
dc.subject.keywordAuthorHirayama disease-
dc.subject.keywordAuthorprogressive muscular atrophy-
dc.subject.keywordAuthorsplit hand-
dc.subject.keywordPlusPROGRESSIVE MUSCULAR-ATROPHY-
dc.subject.keywordPlusDISTAL UPPER EXTREMITY-
dc.subject.keywordPlusSPLIT-HAND-
dc.subject.keywordPlusHIRAYAMA-DISEASE-
dc.subject.keywordPlusALS-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusFEATURES-
dc.subject.keywordPlusTHENAR-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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