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dc.contributor.authorBayrak, Ayse Oytun
dc.contributor.authorBattaloglu, Esra
dc.contributor.authorTurker, Hande
dc.contributor.authorBaris, Ibrahim
dc.contributor.authorOztas, Gurkan
dc.date.accessioned2020-06-21T15:06:27Z
dc.date.available2020-06-21T15:06:27Z
dc.date.issued2009
dc.identifier.issn0387-7604
dc.identifier.urihttps://doi.org/10.1016/j.braindev.2008.07.002
dc.identifier.urihttps://hdl.handle.net/20.500.12712/18612
dc.descriptionbaris, ibrahim/0000-0003-2185-3259en_US
dc.descriptionWOS: 000266272400009en_US
dc.descriptionPubMed: 18760885en_US
dc.description.abstractHereditary neuropathy with liability to pressure palsy (HNPP) is an autosomal dominant disorder characterized by recurrent mono-neuropathies secondary to minor trauma or compression. Whilst typical episodes of palsy generally become apparent during the second and the third decades, HNPP is rarely diagnosed in the first decade. We present the case of a 6-year-old patient to draw attention to the possibility of HNPP attacks in the first decade and the importance of detailed electrophysiological examination. (C) 2008 Elsevier B.V. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Bven_US
dc.relation.isversionof10.1016/j.braindev.2008.07.002en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHereditary neuropathy with liability to pressure palsyen_US
dc.subjectChildhooden_US
dc.subjectElectrophysiologyen_US
dc.titleHereditary neuropathy with liability to pressure palsy (HNPP) in childhood: A case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decadeen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume31en_US
dc.identifier.issue6en_US
dc.identifier.startpage445en_US
dc.identifier.endpage448en_US
dc.relation.journalBrain & Developmenten_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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