Show simple item record

Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation

dc.contributor.authorTepgec, Fatih
dc.contributor.authorAkarsu, Emel Oguz
dc.contributor.authorBaykan, Betul
dc.contributor.authorTekturk, Pinar
dc.contributor.authorYapici, Zuhal
dc.contributor.authorUyguner, Z. Oya
dc.date.accessioned2021-03-04T19:52:46Z
dc.date.available2021-03-04T19:52:46Z
dc.identifier.citationAkarsu E. O. , Tekturk P., Yapici Z., Tepgec F., Uyguner Z. O. , Baykan B., "Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation", SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, cilt.42, ss.49-51, 2016
dc.identifier.issn1059-1311
dc.identifier.othervv_1032021
dc.identifier.otherav_91df1095-9830-4a70-99fb-354d36fd29d9
dc.identifier.urihttp://hdl.handle.net/20.500.12627/98405
dc.identifier.urihttps://doi.org/10.1016/j.seizure.2016.09.007
dc.language.isoeng
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectKlinik Tıp (MED)
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleEyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation
dc.typeMakale
dc.relation.journalSEIZURE-EUROPEAN JOURNAL OF EPILEPSY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume42
dc.identifier.startpage49
dc.identifier.endpage51
dc.contributor.firstauthorID236263


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record