Neuromyelitis optica spectrum disorder: a pediatric case report
| dc.contributor.author | Arslan, Müjgan | |
| dc.contributor.author | Güngör, Serdal | |
| dc.contributor.author | Kılıç, Betül | |
| dc.contributor.author | Karlı Oğuz, Kader | |
| dc.date.accessioned | 2021-11-23T11:01:20Z | |
| dc.date.available | 2021-11-23T11:01:20Z | |
| dc.date.issued | 2017 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | Abstract: Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune demyelinating disorder of the central nervous system that predominantly affects the optic nerves and the spinal cord. Magnetic resonance imaging (MRI) has an increasingly important role in differentiating NMOSD from other inflammatory disorders of the central nervous system, particularly multiple sclerosis (MS). Specific antibodies against aquaporin-4 (AQP4) were identified and found to be directly responsible for the pathogenesis of the disease. We report on an AQP4 antibody-positive 12-year-old female with radiological findings in her brain MRI | en_US |
| dc.identifier.citation | ARSLAN M,GÜNGÖR S,KILIÇ B,OĞUZ K. K (2017). Neuromyelitis optica spectrum disorder: a pediatric case report. Medicine Science, 6(3), 562 - 566. | en_US |
| dc.identifier.endpage | 566 | en_US |
| dc.identifier.issn | 2147-0634 | |
| dc.identifier.issue | 3 | en_US |
| dc.identifier.startpage | 562 | en_US |
| dc.identifier.trdizinid | 264262 | en_US |
| dc.identifier.uri | https://hdl.handle.net/11616/43269 | |
| dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/264262 | |
| dc.identifier.volume | 6 | en_US |
| dc.indekslendigikaynak | TR-Dizin | en_US |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | Medicine Science | en_US |
| dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Neuromyelitis optica spectrum disorder: a pediatric case report | en_US |
| dc.type | Article | en_US |
