Showing results (21-30 of 54) with videos related to
Sort By:
Pageof 6
Noro Psikiyatri Arsivi|March 4, 2026
Posterior Atrophy is a Neuroimaging Marker of Mild Cognitive Impairment in Parkinson's DiseaseUlaş Ay, Zerrin Yıldırım, Ani Kicik, et al.Journal of Medical Genetics|March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.Epilepsy Research|November 12, 2016
Analysis of the tremor in juvenile myoclonic epilepsyZeynep Aydin-Özemir, Zeliha Matur, Betul Baykan, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 15, 2021
A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's diseaseGamze Guven, Bedia Samanci, Cagri Gulec, et al.Behavioural Brain Research|May 24, 2026
Beyond Atrophy: Network-Level Functional Disintegration Pattern Along the Cognitive Decline in Parkinson's DiseaseUlaş Ay, Ani Kicik, Emel Erdogdu, et al.Parkinsonism & Related Disorders|December 18, 2017
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in TurkeyChristoph Kessler, Burcu Atasu, Hasmet Hanagasi, et al.Human Genomics|July 29, 2021
A comprehensive analysis of copy number variation in a Turkish dementia cohortNadia Dehghani, Gamze Guven, Celia Kun-Rodrigues, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 30, 2016
PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset ParkinsonismAnamika Giri, Gamze Guven, Hasmet Hanagasi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.European Journal of Radiology|October 7, 2021
Detection of visual and frontoparietal network perfusion deficits in Parkinson's disease dementiaSena Azamat, Dilek Betul Arslan, Emel Erdogdu, et al.Pageof 6