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dc.contributor.authorSaltik, Sema
dc.contributor.authorSiva, Aksel
dc.contributor.authorYalcinkaya, Cengiz
dc.contributor.authorSaip, Sabahattin
dc.contributor.authorKocer, Naci
dc.date.accessioned2021-03-03T16:05:17Z
dc.date.available2021-03-03T16:05:17Z
dc.date.issued2004
dc.identifier.citationSaltik S., Saip S., Kocer N., Siva A., Yalcinkaya C., "MR1 findings in pediatric neuro-Behcet's disease", NEUROPEDIATRICS, cilt.35, sa.3, ss.190-193, 2004
dc.identifier.issn0174-304X
dc.identifier.othervv_1032021
dc.identifier.otherav_425374ee-7b01-4e87-aa1b-6ec053f46c56
dc.identifier.urihttp://hdl.handle.net/20.500.12627/48319
dc.identifier.urihttps://doi.org/10.1055/s-2004-815826
dc.description.abstractBehcet's disease (BD), a systemic vasculitis of unknown cause, affects many organs and systems. Neurological involvement is seen in 5-15% of the patients, and the two major forms of neurological disease seen in BD are central nervous system (CNS) parenchymal involvement and cerebral venous sinus thrombosis. We report a 14-year-old boy with BD who had neuro-parenchymal involvement. The diagnosis of the systemic disease was not made until the onset of the neurological manifestations, which led to an MRI study that revealed findings suggestive of CNS involvement of BD. We therefore emphasize the importance of the localization and appearance of other characteristics of the lesions on MRI in the differential diagnosis of parenchymal neuro-Behcet syndrome.
dc.language.isoeng
dc.subjectTıp
dc.subjectNöroloji
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectSağlık Bilimleri
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.titleMR1 findings in pediatric neuro-Behcet's disease
dc.typeMakale
dc.relation.journalNEUROPEDIATRICS
dc.contributor.departmentİstanbul Üniversitesi , Cerrahpaşa Tıp Fakültesi , Nöroloji
dc.identifier.volume35
dc.identifier.issue3
dc.identifier.startpage190
dc.identifier.endpage193
dc.contributor.firstauthorID23042


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