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dc.contributor.authorBayrak A.O.
dc.contributor.authorBattaloğlu E.
dc.contributor.authorAkar H.
dc.contributor.authorBariş I.
dc.contributor.authorOnar M.K.
dc.date.accessioned2020-06-21T09:27:48Z
dc.date.available2020-06-21T09:27:48Z
dc.date.issued2010
dc.identifier.issn1301-062X
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4169
dc.description.abstractHereditary neuropathy with liability to pressure palsy (HNPP) is an autosomal dominant disorder characterized by acute, painless and recurrent mononeuropathies that are secondary to minor trauma or compression. Diagnosis is often overlooked when detailed examinations are not performed. We discuss the features of our four HNPP patients and their close relatives in order to emphasize the importance of clinical and electrophysiological findings in the diagnosis of HNPP. Four patients and three members of the family underwent genetic testing and HBDN deletion was shown in all.en_US
dc.language.isoturen_US
dc.publisherTurkish Neurosurgical Societyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectElectrophysiologyen_US
dc.subjectHereditaryen_US
dc.subjectLiability to pressure palsiesen_US
dc.subjectNeuropathyen_US
dc.titleHereditary neuropathy with liability to pressure palsy: The clinical and electrophysiological features of four familiesen_US
dc.title.alternativeHerediter Basınca Duyarlı Nöropati: Dört Ailenin Klinik ve Elektrofizyolojik Özelliklerien_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume16en_US
dc.identifier.issue4en_US
dc.identifier.startpage193en_US
dc.identifier.endpage198en_US
dc.relation.journalTurk Noroloji Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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