Ве молиме користете го овој идентификатор да го цитирате или поврзете овој запис: http://hdl.handle.net/20.500.12188/11816
DC FieldValueLanguage
dc.contributor.authorEmilija Cvetkovskaen_US
dc.contributor.authorIgor Kuzmanovskien_US
dc.contributor.authorMarija Babunovskaen_US
dc.contributor.authorBojan Boshkovskien_US
dc.contributor.authorTatjana Cepreganova Cangovskaen_US
dc.contributor.authorGordana Kiteva Trencevskaen_US
dc.date.accessioned2021-04-12T09:00:16Z-
dc.date.available2021-04-12T09:00:16Z-
dc.date.issued2018-05-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/11816-
dc.description.abstractThe traditional perception of mesial temporal lobe epilepsy (MTLE) as a predominantly acquired disorder is challenged due to emerging evidence of familial aggregation. In this study, we ascertained the extent of familial occurrence of epilepsy in MTLE patients, as well as phenotypic heterogeneity in affected relatives.en_US
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofSeizureen_US
dc.titlePhenotypic spectrum in families with mesial temporal lobe epilepsy probandsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.seizure.2018.03.019-
dc.identifier.urlhttps://api.elsevier.com/content/article/PII:S1059131117308324?httpAccept=text/xml-
dc.identifier.urlhttps://api.elsevier.com/content/article/PII:S1059131117308324?httpAccept=text/plain-
dc.identifier.volume58-
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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