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Neurological Research|July 9, 2025
The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson's diseaseBranislava Radojević, Andona Milovanović, Igor Petrović, et al.
Journal of Neurology|April 4, 2023
Long-term outcome of patients with neurological form of Wilson's disease compliant to the de-coppering treatmentIva Stanković, Čarna Jovanović, Jelena Vitković, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 15, 2014
De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patientValerija Dobričić, Nikola Kresojević, Ana Westenberger, et al.
Journal of Neurology|January 7, 2022
Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experienceNikola Kresojević, Valerija Dobričić, Milica Ječmenica Lukić, et al.
Parkinsonism & Related Disorders|April 10, 2022
The correlation between genetic factors and freezing of gait in patients with Parkinson's diseaseBranislava Radojević, Nataša T Dragašević-Mišković, Ana Marjanović, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2010
Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15Anne Weissbach, Ana Djarmati, Christine Klein, et al.
Journal of Parkinson'S Disease|June 21, 2021
Clinical and Genetic Analysis of Psychosis in Parkinson's DiseaseBranislava Radojević, Nataša T Dragašević-Mišković, Ana Marjanović, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 22, 2021
Longitudinal White Matter Damage Evolution in Parkinson's DiseasePietro Giuseppe Scamarcia, Federica Agosta, Edoardo Gioele Spinelli, et al.
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