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Jeavons Syndrome: 12 Cases

dc.contributor.authorTopaloglu Tuac, Selma
dc.contributor.authorYalcinkaya, Cengiz
dc.contributor.authorDemirbilek, Ahmet Veysi
dc.date.accessioned2021-03-04T10:36:01Z
dc.date.available2021-03-04T10:36:01Z
dc.date.issued2017
dc.identifier.citationTopaloglu Tuac S., Yalcinkaya C., Demirbilek A. V. , "Jeavons Syndrome: 12 Cases", EPILEPSI, cilt.23, sa.2, ss.72-76, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_6e034edf-ba24-418b-bd46-a66ae69678e1
dc.identifier.urihttp://hdl.handle.net/20.500.12627/75963
dc.identifier.urihttps://doi.org/10.14744/epilepsi.2016.88319
dc.description.abstractObjectives: 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.isoeng
dc.subjectTıp
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleJeavons Syndrome: 12 Cases
dc.typeMakale
dc.relation.journalEPILEPSI
dc.contributor.departmentIstanbul Bakirkoy Mental Health & Neurology Training & Research Hospital , ,
dc.identifier.volume23
dc.identifier.issue2
dc.identifier.startpage72
dc.identifier.endpage76
dc.contributor.firstauthorID238915


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