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Whole exome sequencing in Serbian patients with hereditary spastic paraplegia.
Brankovic M, Ivanovic V, Basta I, Khang R, Lee E, Stevic Z, Ralic B, Tubic R, Seo G, Markovic V, Bozovic I, Svetel M, Marjanovic A, Veselinovic N, Mesaros S, Jankovic M, Savic-Pavicevic D, Jovin Z, Novakovic I, Lee H, Peric S. Brankovic M, et al. Among authors: svetel m. Neurogenetics. 2024 Mar 19. doi: 10.1007/s10048-024-00755-x. Online ahead of print. Neurogenetics. 2024. PMID: 38499745
Presenting symptoms of GBA-related Parkinson's disease.
Kresojević N, Janković M, Petrović I, Kumar KR, Dragašević N, Dobričić V, Novaković I, Svetel M, Klein C, Pekmezović T, Kostić VS. Kresojević N, et al. Among authors: svetel m. Parkinsonism Relat Disord. 2015 Jul;21(7):804-7. doi: 10.1016/j.parkreldis.2015.04.028. Epub 2015 May 1. Parkinsonism Relat Disord. 2015. PMID: 25957717
Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited.
Dobričić V, Kresojević N, Žarković M, Tomić A, Marjanović A, Westenberger A, Cvetković D, Svetel M, Novaković I, Kostić VS. Dobričić V, et al. Among authors: svetel m. Parkinsonism Relat Disord. 2015 Oct;21(10):1256-9. doi: 10.1016/j.parkreldis.2015.08.001. Epub 2015 Aug 10. Parkinsonism Relat Disord. 2015. PMID: 26297380
HPCA-related dystonia: Too rare to be found?
Dobričić V, Kresojević N, Marjanović A, Tomić A, Svetel M, Novaković I, Kostić VS. Dobričić V, et al. Among authors: svetel m. Mov Disord. 2016 Jul;31(7):1071. doi: 10.1002/mds.26634. Epub 2016 May 4. Mov Disord. 2016. PMID: 27145302 No abstract available.
165 results