Browsing by ORCID "Demet Özbabalık Adapınar /0000-0002-3650-2876"
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A Case of CADASIL with NOTCH3 Gene Mutation Presenting with Focal Epileptic Seizure: A Case of CADASIL Presenting with Focal Epileptic Seizure
Uncu, Gülgün; Algın, Demet İlhan; Erdinç, Oğuz Osman; Adapınar, Demet Özbabalık (Galenos Publishing House, 2023)CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is a hereditary disease of cerebral microvessels with autosomal dominant inheritance due to the NOTCH3 gene mutation. ...