dc.contributor.author | Topaloglu Tuac, Selma | |
dc.contributor.author | Yalcinkaya, Cengiz | |
dc.contributor.author | Demirbilek, Ahmet Veysi | |
dc.date.accessioned | 2021-03-04T10:36:01Z | |
dc.date.available | 2021-03-04T10:36:01Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Topaloglu Tuac S., Yalcinkaya C., Demirbilek A. V. , "Jeavons Syndrome: 12 Cases", EPILEPSI, cilt.23, sa.2, ss.72-76, 2017 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_6e034edf-ba24-418b-bd46-a66ae69678e1 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/75963 | |
dc.identifier.uri | https://doi.org/10.14744/epilepsi.2016.88319 | |
dc.description.abstract | Objectives: Jeavons Syndrome (JS), also known as eyelid myoclonia with absences epilepsy, is a type of idiopathic reflex epilepsy that has primary seizure type eyelid myoclonuses and is characterized by blinking due to seizures or generalized paroxysms at electroencephalography (EEG) and photosensitivity. This study aimed to review JS by following up with the patients with this diagnosis. | |
dc.language.iso | eng | |
dc.subject | Tıp | |
dc.subject | Nöroloji | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | KLİNİK NEUROLOJİ | |
dc.title | Jeavons Syndrome: 12 Cases | |
dc.type | Makale | |
dc.relation.journal | EPILEPSI | |
dc.contributor.department | Istanbul Bakirkoy Mental Health & Neurology Training & Research Hospital , , | |
dc.identifier.volume | 23 | |
dc.identifier.issue | 2 | |
dc.identifier.startpage | 72 | |
dc.identifier.endpage | 76 | |
dc.contributor.firstauthorID | 238915 | |