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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 26, 2025
Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?Nikola Kresojević, Vladana Marković, Cveta Geratović, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2024
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case SeriesAndona Milovanović, Ana Westenberger, Iva Stanković, et al.
Cells|September 23, 2022
Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from SerbiaStojan Perić, Vladana Marković, Ayşe Candayan, et al.
Genes|May 4, 2026
Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's DiseaseGaber Bergant, Vesna M van Midden, Polina Tsygankova, et al.
Parkinsonism & Related Disorders|June 19, 2018
Axial motor clues to identify atypical parkinsonism: A multicentre European cohort studyCarlijn D J M Borm, Florian Krismer, Gregor K Wenning, et al.
Nature Genetics|August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and miceAnnika Keller, Ana Westenberger, Maria J Sobrido, et al.
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