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dc.contributor.authorTerzi, Murat
dc.contributor.authorYazici, Tuba
dc.contributor.authorAkdemir, Neslihan
dc.contributor.authorTerzi, Tuley
dc.contributor.authorOnar, Musa
dc.date.accessioned2020-06-21T14:39:38Z
dc.date.available2020-06-21T14:39:38Z
dc.date.issued2011
dc.identifier.issn1300-0667
dc.identifier.issn1309-4866
dc.identifier.urihttps://doi.org/10.4274/Npa.Y5787
dc.identifier.urihttps://hdl.handle.net/20.500.12712/17035
dc.descriptionWOS: 000295698900012en_US
dc.description.abstractSjogren's syndrome is a slowly progressive autoimmune disease. Neurological involvement is seen in approximately 20-25% of all cases of Sjogren's syndrome - 87% in the peripheral nervous system and almost 13% in the central nervous system. Neuromyelitis Optica (NMO)-like clinical picture is quite rare in Sjogren's syndrome. We present clinical and radiological features mimicking NMO spectrum disorder in two patients who were diagnosed with Sjogren's syndrome after investigation. In such cases, the early diagnosis and treatment of Sjogren's syndrome is of great importance for the prognosis of the disease. (Archives of Neuropsychiatry 2011; 48: 221-3)en_US
dc.language.isoturen_US
dc.publisherTurkish Neuropsychiatry Assoc-Turk Noropsikiyatri Dernegien_US
dc.relation.isversionof10.4274/Npa.Y5787en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSjogren's Syndromeen_US
dc.subjectcentral nervous systemen_US
dc.subjectoptic neuritisen_US
dc.subjectmyelitisen_US
dc.titleNeuromyelitis Optica Spectrum Disorder in Sjogren's Syndromeen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume48en_US
dc.identifier.issue3en_US
dc.identifier.startpage221en_US
dc.identifier.endpage223en_US
dc.relation.journalNoropsikiyatri Arsivi-Archives of Neuropsychiatryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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