Yazar "Adapınar, Demet Özbabalık" için listeleme
-
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: ... -
Frequency of frontotemporal dementia-related gene variants in Turkey
Artan, Sevilhan; Gökalp, Ebru Erzurumluoğlu; Samanci, Bedia; Bas, Hasan; Tepgec, Fatih; Ekenel, Emilia Qomi; Cilingir, Oguz; Bilgic, Basar; Gurvit, Hakan; Hanagasi, Hasmet Ayhan; Kocagil, Sinem; Aras, Beyhan Durak; Uyguner, Oya; Emre, Murat (Elsevier Science İnc, 2021)Frontotemporal demansın (FTD) klinik heterojenliği gibi genetik temeli de çeşitlidir ve hastalık patogenezinde çok sayıda moleküler yolakların rol oynadığı düşünülmektedir. Bu çalışmada FTD ile ilişkili genler, 175 indeks ...
