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- W3082945211 abstract "CADASIL (Cerebral Autosomal Dominant Arteriopati, Subcortical Infarcts, Leukoencephalopathy) 19. kromozomun kisa kolunda lokalize Notch3 gen mutasyonu sonucu gelisen otozomal dominant gecisli ailesel kucuk damar hastaligidir. Klinik olarak tekrarlayan inme ataklari, migren veya migrenoz basagrilari, epileptik nobetler ve progresif kognitif bozukluk ile karakterizedir. Bu yazida klinik olarak CADASIL dusundugumuz, molekuler calisma ile CADASIL tanisini konfirme ettigimiz dort olgu klinik ve genetik ozellikleri ile sunulmustur." @default.
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- W3082945211 date "2021-01-21" @default.
- W3082945211 modified "2023-09-27" @default.
- W3082945211 title "CADASIL: Klinik-Genetik Korelasyon" @default.
- W3082945211 doi "https://doi.org/10.20515/otd.737592" @default.
- W3082945211 hasPublicationYear "2021" @default.
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