Pitfalls in the diagnosis of Jeavons syndrome: a study of 32 cases and review of the literature

dc.contributor.author	Reyhani, Aylin
dc.contributor.author	ÖZKARA, Çiğdem
dc.date.accessioned	2021-03-02T18:11:53Z
dc.date.available	2021-03-02T18:11:53Z
dc.date.issued	2020
dc.identifier.citation	Reyhani A., ÖZKARA Ç., "Pitfalls in the diagnosis of Jeavons syndrome: a study of 32 cases and review of the literature", EPILEPTIC DISORDERS, cilt.22, sa.3, ss.281-290, 2020
dc.identifier.issn	1294-9361
dc.identifier.other	av_18922fe0-8f9b-490b-b9c0-9a53e67fbcc2
dc.identifier.other	vv_1032021
dc.identifier.uri	http://hdl.handle.net/20.500.12627/4665
dc.identifier.uri	https://doi.org/10.1684/epd.2020.1162
dc.description.abstract	Aims. Jeavons syndrome (JS) is mainly characterized by eyelid myoclonia with or without absences. It is thought to be underdiagnosed rather than have a rare prevalence. We aimed to investigate the electroclinical features of JS to determine possible factors influencing the diagnosis.
dc.language.iso	eng
dc.subject	Dahili Tıp Bilimleri
dc.subject	Nöroloji
dc.subject	Sağlık Bilimleri
dc.subject	Tıp
dc.subject	Klinik Tıp (MED)
dc.subject	Klinik Tıp
dc.subject	KLİNİK NEUROLOJİ
dc.title	Pitfalls in the diagnosis of Jeavons syndrome: a study of 32 cases and review of the literature
dc.type	Makale
dc.relation.journal	EPILEPTIC DISORDERS
dc.contributor.department	Fatih Sultan Mehmet Training & Research Hospital , ,
dc.identifier.volume	22
dc.identifier.issue	3
dc.identifier.startpage	281
dc.identifier.endpage	290
dc.contributor.firstauthorID	2282419

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