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dc.contributor.authorKantarci, Orhun H.
dc.contributor.authorSiva, Aksel
dc.contributor.authorPelletier, Daniel
dc.contributor.authorOkuda, Darin T.
dc.contributor.authorLebrun, Christine
dc.date.accessioned2021-03-03T19:04:04Z
dc.date.available2021-03-03T19:04:04Z
dc.date.issued2018
dc.identifier.citationLebrun C., Kantarci O. H. , Siva A., Pelletier D., Okuda D. T. , "Anomalies Characteristic of Central Nervous System Demyelination Radiologically Isolated Syndrome", NEUROLOGIC CLINICS, cilt.36, sa.1, ss.59-69, 2018
dc.identifier.issn0733-8619
dc.identifier.otherav_528ea61b-47c7-4cb1-ab95-c376830e18a6
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/58594
dc.identifier.urihttps://doi.org/10.1016/j.ncl.2017.08.004
dc.description.abstractRadiologically isolated syndrome (RIS) was defined in 2009 for asymptomatic patients who presented incidentally identified white matter anomalies within the central nervous system suggestive of multiple sclerosis (MS). Approximately one-third of RIS subjects will have a seminal clinical demyelinating event within 5 years of the identification of their abnormal MRI. Clinical evolution mirrors relapsing remitting or progressive forms of MS. Pejorative factors for clinical conversion are male gender, age younger than 35 years, and spinal cord lesions.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSinirbilim ve Davranış
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleAnomalies Characteristic of Central Nervous System Demyelination Radiologically Isolated Syndrome
dc.typeMakale
dc.relation.journalNEUROLOGIC CLINICS
dc.contributor.departmentCHU Nice , ,
dc.identifier.volume36
dc.identifier.issue1
dc.identifier.startpage59
dc.identifier.endpage69
dc.contributor.firstauthorID251426


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