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dc.contributor.authorYilmaz, Onat
dc.contributor.authorAbali, Osman
dc.date.accessioned2021-03-06T21:14:20Z
dc.date.available2021-03-06T21:14:20Z
dc.date.issued2012
dc.identifier.citationYilmaz O., Abali O., "Kleine-Levin Syndrome Treated with Carbamazepine: A Case Report", NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, cilt.49, ss.71-73, 2012
dc.identifier.issn1300-0667
dc.identifier.otherav_fdcd8e77-160e-4586-8282-45b704d88f41
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/166019
dc.identifier.urihttps://doi.org/10.4274/npa.y5836
dc.description.abstractKleine-Levin syndrome (KLS) is characterized by recurrent episodes of hypersomnia frequently associated with behavioral or cognitive disturbances, compulsive eating behavior, and hypersexuality. Although the syndrome is rare, it is important that clinicians be aware of this syndrome and distinguish it from organic or psychiatric diseases with more serious prognoses. Here, we report the case of a 14-year-old adolescent male with KLS, who showed significant improvement with carbamazepine during follow-up to age 26. This study describes the clinical course of KLS and results of long-term follow-up of carbamazepine treatment. (Archives of Neuropsychiatry 2012;49: 71-3)
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleKleine-Levin Syndrome Treated with Carbamazepine: A Case Report
dc.typeMakale
dc.relation.journalNOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
dc.contributor.departmentGulhane Military Medical Academy , ,
dc.identifier.volume49
dc.identifier.issue1
dc.identifier.startpage71
dc.identifier.endpage73
dc.contributor.firstauthorID203020


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