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Autosomal Dominant Cortical Tremor, Myoclonus, and Epilepsy Syndrome mimicking Juvenile Myoclonic Epilepsy

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dc.contributor.authorAydin Ozemir, Zeynep
dc.contributor.authorOguz Akarsu, Emel
dc.contributor.authorMatur, ZELİHA
dc.contributor.authorOge, Ali Emre
dc.contributor.authorBAYKAL, Betül
dc.contributor.institutionauthorMATUR, ZELİHA
dc.date.accessioned2022-01-13T20:59:20Z
dc.date.available2022-01-13T20:59:20Z
dc.date.issued2016-09-01T00:00:00Z
dc.description.abstractIntroduction: Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) syndrome is a genetically heterogeneous and under-recognized disease characterized by tremulous movements mimicking essential tremor, myoclonus, and rare generalized tonic-clonic seizures. Here we described the clinical and electrophysiological features of three siblings with ADCME syndrome mimicking juvenile myoclonic epilepsy (JME).
dc.identifier.citationAydin Ozemir Z., Oguz Akarsu E., Matur Z., Oge A. E. , BAYKAL B., -Autosomal Dominant Cortical Tremor, Myoclonus, and Epilepsy Syndrome mimicking Juvenile Myoclonic Epilepsy-, NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, cilt.53, sa.3, ss.272-275, 2016
dc.identifier.doi10.5152/npa.2016.14841
dc.identifier.scopus84983371758
dc.identifier.urihttp://hdl.handle.net/20.500.12645/30133
dc.identifier.wosWOS:000383254700015
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleAutosomal Dominant Cortical Tremor, Myoclonus, and Epilepsy Syndrome mimicking Juvenile Myoclonic Epilepsy
dc.typeArticle
dspace.entity.typePublication
local.avesis.id0e6220a1-3216-43e2-9b88-ca1591c5e190
local.publication.isinternational1
relation.isAuthorOfPublication3c69fce6-5ba0-4838-9215-eae7a7125446
relation.isAuthorOfPublication.latestForDiscovery3c69fce6-5ba0-4838-9215-eae7a7125446
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