Vesna Brankovic
Belgrade, SE, Serbia
Last Updated: 09/26/2026
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Found 10 publications
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series.
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 11, 2023
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 29, 2021
A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine.
Journal: International journal of molecular sciences
Published: July 15, 2021
Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study.
Journal: Journal of medical genetics
Published: November 05, 2020
Novel unconventional variants expand the allelic spectrum of OPHN1 gene.
Journal: American journal of medical genetics. Part A
Published: September 25, 2020
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome.
Journal: Epilepsia
Published: June 05, 2020
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders.
Journal: Journal of medical genetics
Published: March 16, 2020
Phenotype of PLP1-related Disorder Caused by Novel Mutation: A Case Report.
Journal: Movement disorders clinical practice
Published: January 29, 2018
GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia.
Journal: Parkinsonism & related disorders
Published: April 17, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026