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dc.contributor.authorCoban, Arzu
dc.contributor.authorTuzun, Erdem
dc.contributor.authorShugaiv, Erkingul
dc.date.accessioned2021-03-04T15:10:47Z
dc.date.available2021-03-04T15:10:47Z
dc.identifier.citationCoban A., Shugaiv E., Tuzun E., "Syndrome of Headache Accompanied with Transient Neurologic Deficits and Cerebrospinal Fluid Lymphocytosis", NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, cilt.50, ss.52-55, 2013
dc.identifier.issn1300-0667
dc.identifier.othervv_1032021
dc.identifier.otherav_8565938d-4047-47fc-9a80-ef2ae630c5b7
dc.identifier.urihttp://hdl.handle.net/20.500.12627/90703
dc.identifier.urihttps://doi.org/10.4274/npa.y7228
dc.description.abstractThe syndrome of headache accompanied with transient neurologic deficits and cerebrospinal fluid lymphocytosis (HaNDL), is a rare, benign and self limiting syndrome. In the 2nd Edition of the International Classification of Headache Disorders, HaNDL syndrome was defined in secondary headache group as "Headache attributed to non-vascular intracranial disorder". The etiology of HaNDL is still unknown. In recent years, some authors have shown that ion channel autoimmunity might at least partially contribute to HaNDL pathogenesis. In this paper, the definition of HaNDL syndrome, clinical picture and epidemiology of HaNDL syndrome, etiopathogenesis, differential diagnosis and treatment will be reviewed with the recent literature.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleSyndrome of Headache Accompanied with Transient Neurologic Deficits and Cerebrospinal Fluid Lymphocytosis
dc.typeMakale
dc.relation.journalNOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume50
dc.identifier.startpage52
dc.identifier.endpage55
dc.contributor.firstauthorID2239


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