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dc.contributor.authorSakalli, Karagoz N.
dc.contributor.authorTopcular, Barış
dc.contributor.authorOzcan, M. E.
dc.contributor.authorKirbas, DURSUN
dc.contributor.authorGul, Gülsen
dc.contributor.authorAslan, Kalyoncu
dc.date.accessioned2021-03-06T10:24:43Z
dc.date.available2021-03-06T10:24:43Z
dc.identifier.citationKirbas D., Topcular B., Ozcan M. E. , Sakalli K. N. , Gul G., Aslan K., "IDIOPATHIC TOLOSA-HUNT SYNDROME: FOUR ADDITIONAL CASES", IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE, cilt.61, ss.250-254, 2008
dc.identifier.issn0019-1442
dc.identifier.othervv_1032021
dc.identifier.otherav_ea3fd196-2ae4-4eac-b468-e69df9d47647
dc.identifier.urihttp://hdl.handle.net/20.500.12627/153864
dc.description.abstractIdiopathic Tolosa Hunt syndrome (ITHS) is a very rare cause of painful ophthalmoplegia characterized by unilateral orbital pain, ipsilateral oculomotor paralysis and prompt response to steroids. In this paper we report 4 additional cases of ITHS. This rare cause of painful ophthalmoplegia effects the cranial nerves due to a granulomatous lesion of unknown etiology in the cavernous sinus or superior orbital fissure. The International Headache Society redefined the diagnostic criteria for ITHS but it is still mostly a diagnosis of exclusion. Careful evaluation and follow-up is essential for diagnosis. Optimal therapy duration and dosage and prophylactic treatment in recurrent cases needs further research.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleIDIOPATHIC TOLOSA-HUNT SYNDROME: FOUR ADDITIONAL CASES
dc.typeMakale
dc.relation.journalIDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE
dc.contributor.departmentIstanbul Bakirkoy Mental Health & Neurology Training & Research Hospital , ,
dc.identifier.volume61
dc.identifier.startpage250
dc.identifier.endpage254
dc.contributor.firstauthorID90102


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