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EEG Findings in Patients with Rett Syndrome

dc.contributor.authorOge, Ali Emre
dc.contributor.authorEraksoy, Mefkure
dc.contributor.authorGurses, Candan
dc.contributor.authorYapici, Zuhal
dc.contributor.authorAyta, Semih
dc.date.accessioned2021-03-04T08:29:52Z
dc.date.available2021-03-04T08:29:52Z
dc.date.issued2017
dc.identifier.citationAyta S., Oge A. E. , Gurses C., Yapici Z., Eraksoy M., "EEG Findings in Patients with Rett Syndrome", EPILEPSI, cilt.23, sa.2, ss.63-71, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_63999373-fa7a-4f51-bdc1-11b068814b38
dc.identifier.urihttp://hdl.handle.net/20.500.12627/69343
dc.identifier.urihttps://doi.org/10.14744/epilepsi.2017.28199
dc.description.abstractObjectives: Rett syndrome (RS) is a neurodevelopmental disorder that primarily affects girls and is characterized by microcephaly, regression of language, loss of effective hand use, epilepsy, and electroencephalogram (EEG) abnormalities. This study investigated EEG findings of 12 female patients diagnosed with RS.
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.titleEEG Findings in Patients with Rett Syndrome
dc.typeMakale
dc.relation.journalEPILEPSI
dc.contributor.departmentIstanbul Haseki Training & Research Hospital , ,
dc.identifier.volume23
dc.identifier.issue2
dc.identifier.startpage63
dc.identifier.endpage71
dc.contributor.firstauthorID238817


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