Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/11816| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Emilija Cvetkovska | en_US |
| dc.contributor.author | Igor Kuzmanovski | en_US |
| dc.contributor.author | Marija Babunovska | en_US |
| dc.contributor.author | Bojan Boshkovski | en_US |
| dc.contributor.author | Tatjana Cepreganova Cangovska | en_US |
| dc.contributor.author | Gordana Kiteva Trencevska | en_US |
| dc.date.accessioned | 2021-04-12T09:00:16Z | - |
| dc.date.available | 2021-04-12T09:00:16Z | - |
| dc.date.issued | 2018-05 | - |
| dc.identifier.uri | http://hdl.handle.net/20.500.12188/11816 | - |
| dc.description.abstract | The 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.iso | en | en_US |
| dc.publisher | Elsevier BV | en_US |
| dc.relation.ispartof | Seizure | en_US |
| dc.title | Phenotypic spectrum in families with mesial temporal lobe epilepsy probands | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | 10.1016/j.seizure.2018.03.019 | - |
| dc.identifier.url | https://api.elsevier.com/content/article/PII:S1059131117308324?httpAccept=text/xml | - |
| dc.identifier.url | https://api.elsevier.com/content/article/PII:S1059131117308324?httpAccept=text/plain | - |
| dc.identifier.volume | 58 | - |
| item.fulltext | No Fulltext | - |
| item.grantfulltext | none | - |
| crisitem.author.dept | Faculty of Medicine | - |
| crisitem.author.dept | Faculty of Medicine | - |
| Appears in Collections: | Faculty of Medicine: Journal Articles | |
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