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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. ... -
Evaluation of cognitive deficits in patients infected with COVID-19
Arica-Polat, B. S.; Gündoğdu, A. A.; Cinar, N.; Uncu, Gülgün; Ayas, Z. O.; Iseri, P.; Karadas, O.; Adapınar, Demet Özbabalık (Verduci Publisher, 2022)OBJECTIVE: COVID-19 infection can cause impairments in many cognitive areas. The aim of the present study was to evaluate the cognitive functions of patients who had been infected with COVID-19. PATIENTS AND METHODS: ...
