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dc.contributor.authorBaykan, Betul
dc.contributor.authorAras, Yavuz
dc.contributor.authorBilgic, Bilge
dc.contributor.authorBebek, Nerses
dc.contributor.authorSabanci, Pulat Akin
dc.contributor.authorTimer, Emin
dc.contributor.authorCharsouei, Saeid
dc.contributor.authorIzgi, Nail
dc.contributor.authorGurses, Candan
dc.date.accessioned2021-03-04T10:11:17Z
dc.date.available2021-03-04T10:11:17Z
dc.identifier.citationTimer E., Charsouei S., Bebek N., Baykan B., Bilgic B., Sabanci P. A. , Aras Y., Izgi N., Gurses C., "Neurosurgical treatment of nonconvulsive status epilepticus due to focal cortical dysplasia", EPILEPSY & BEHAVIOR CASE REPORTS, cilt.10, ss.4-7, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_6becf9ae-1a90-400f-bc96-e06fc7aab5ab
dc.identifier.urihttp://hdl.handle.net/20.500.12627/74621
dc.identifier.urihttps://doi.org/10.1016/j.ebcr.2018.03.003
dc.description.abstractWe present a rare case of focal cortical dysplasia (FCD) and nonconvulsive status epilepticus (NCSE) treated successfully with early surgical intervention. Our case is a 9-year-old boy whose seizures, characterized by short episodes of loss of consciousness, appeared at the age of 7, and he showed progressive cognitive decline in the following years. NCSE was diagnosed, and his MRI revealed FCD in the left frontal region which was the same side as his EEG abnormality. Following lesionectomy, his NCSE disappeared and cognitive functions improved. Histopathologic analysis of the resected tissue revealed type-IIB FCD. This case illustrates the importance of early surgery to help restore cognitive functions by eliminating the clinical and electrophysiological features of NCSE. (C) 2018 The Authors. Published by Elsevier Inc.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleNeurosurgical treatment of nonconvulsive status epilepticus due to focal cortical dysplasia
dc.typeMakale
dc.relation.journalEPILEPSY & BEHAVIOR CASE REPORTS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume10
dc.identifier.startpage4
dc.identifier.endpage7
dc.contributor.firstauthorID249852


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