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Clinical and electrophysiological findings in patients with phenylketonuria and epilepsy: Reflex features

dc.contributor.authorGokyigit, Aysen
dc.contributor.authorBebek, Nerses
dc.contributor.authorGurses, Candan
dc.contributor.authorBaykan, Betul
dc.contributor.authorCelik, Senay Yildiz
dc.date.accessioned2021-03-03T13:50:34Z
dc.date.available2021-03-03T13:50:34Z
dc.identifier.citationCelik S. Y. , Bebek N., Gurses C., Baykan B., Gokyigit A., "Clinical and electrophysiological findings in patients with phenylketonuria and epilepsy: Reflex features", EPILEPSY & BEHAVIOR, cilt.82, ss.46-51, 2018
dc.identifier.issn1525-5050
dc.identifier.othervv_1032021
dc.identifier.otherav_365b6611-9c0d-41c4-b33f-7053054f4ecf
dc.identifier.urihttp://hdl.handle.net/20.500.12627/40705
dc.identifier.urihttps://doi.org/10.1016/j.yebeh.2018.02.024
dc.description.abstractObjective: Phenyl ketonuria (PKU) is the most common form of amino acid metabolism disorders with autosomal recessive inheritance. The brain damage can be prevented by early diagnosis and a phenylalanine-restricted diet. Untreated or late-treated patients may show mental retardation and other cognitive dysfunctions, as well as motor disability and/or epilepsy.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectSosyal ve Beşeri Bilimler
dc.subjectDavranış Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectKlinik Tıp (MED)
dc.subjectPsikiyatri
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSinirbilim ve Davranış
dc.subjectDAVRANIŞ BİLİMLERİ
dc.titleClinical and electrophysiological findings in patients with phenylketonuria and epilepsy: Reflex features
dc.typeMakale
dc.relation.journalEPILEPSY & BEHAVIOR
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume82
dc.identifier.startpage46
dc.identifier.endpage51
dc.contributor.firstauthorID252834


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