Myopathy with muscle hypertrophy as a rare presenting feature of primary amyloidosis

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dc.contributor.authorCiftci, S.
dc.contributor.authorYuceyar, A. N.
dc.contributor.authorEkmekci, O.
dc.contributor.authorArgin, M.
dc.contributor.authorKarasoy, H.
dc.date.accessioned2019-10-27T22:15:09Z
dc.date.available2019-10-27T22:15:09Z
dc.date.issued2014
dc.departmentEge Üniversitesien_US
dc.descriptionJoint Congress of European Neurology -- MAY 31-JUN 03, 2014 -- Istanbul, TURKEYen_US
dc.description.sponsorshipEuropean Federat Neurol Socen_US
dc.identifier.endpage520en_US
dc.identifier.issn1351-5101
dc.identifier.issn1468-1331
dc.identifier.startpage520en_US
dc.identifier.urihttps://hdl.handle.net/11454/50128
dc.identifier.volume21en_US
dc.identifier.wosWOS:000337563601207en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.relation.ispartofEuropean Journal of Neurologyen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleMyopathy with muscle hypertrophy as a rare presenting feature of primary amyloidosisen_US
dc.typeConference Objecten_US

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