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dc.contributor.authorBilginer, Burçak
dc.contributor.authorİlhan Algın, Demet
dc.contributor.authorTezer, F Irsel
dc.contributor.authorK Oguz, Kader
dc.contributor.authorSoylemezoglu, Figen
dc.contributor.authorSaygi, Serap
dc.date.accessioned2020-12-07T11:36:27Z
dc.date.available2020-12-07T11:36:27Z
dc.date.issued2019
dc.identifier.issn0967-5868
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/30962059/
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0967586819303704
dc.identifier.urihttp://hdl.handle.net/11655/23162
dc.identifier.urihttps://doi.org/10.1016/j.jocn.2019.03.055
dc.description.abstractNeurofibromatosis type 1 (NF1) is an autosomal dominantly inherited disorder, with an estimated prevalence of 1 in 3000-4000 people. Seizures occur 4-7% of individuals with NF1, mostly due to associated brain tumors or cortical malformations. Hippocampal sclerosis (HS) in the patients with NF1 has been reported very rarely and only 15 patients were found in review of English literature. We presented here 3 additional patients with NF1 and intractable seizures due to hippocampal sclerosis; in whom one of them underwent epilepsy surgery and he is seizure free for 5 years after right temporal lobectomy.tr_TR
dc.language.isoturtr_TR
dc.publisherElseviertr_TR
dc.relation.isversionof10.1016/j.jocn.2019.03.055tr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.rightsAttribution 4.0 United States
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectNeurofibromatosis.tr_TR
dc.subjectIntractable seizures epilepsy surgerytr_TR
dc.subjectHippocampal sclerosistr_TR
dc.titlePharmacoresistant seizures in neurofibromatosis type 1 related to hippocampal sclerosis: Three case presentation and reviewtr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.relation.journalJ Clin Neuroscitr_TR
dc.contributor.departmentBeyin ve Sinir Cerrahisitr_TR
dc.identifier.volumeJuntr_TR
dc.identifier.issue64tr_TR
dc.identifier.startpage14tr_TR
dc.identifier.endpage17tr_TR
dc.description.indexWoStr_TR
dc.fundingYoktr_TR


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