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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: novakovic i. Neurogenetics. 2024 Mar 19. doi: 10.1007/s10048-024-00755-x. Online ahead of print. Neurogenetics. 2024. PMID: 38499745
Yield of the PMP22 deletion analysis in patients with compression neuropathies.
Ivanovic V, Brankovic M, Bjelica B, Kacar A, Tubic R, Jankovic M, Marjanovic A, Novakovic I, Rakocevic-Stojanovic V, Peric S. Ivanovic V, et al. Among authors: novakovic i. J Neurol. 2020 Dec;267(12):3617-3623. doi: 10.1007/s00415-020-10052-w. Epub 2020 Jul 8. J Neurol. 2020. PMID: 32642785
Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
Perić S, Marković V, Candayan A, De Vriendt E, Momčilović N, Savić A, Dragašević-Mišković N, Svetel M, Stević Z, Božović I, Mesaroš Š, Drulović J, Basta I, Petrović I, Tamaš O, Mijajlović M, Novaković I, Sokić D, Jordanova A. Perić S, et al. Among authors: novakovic i. Cells. 2022 Sep 8;11(18):2804. doi: 10.3390/cells11182804. Cells. 2022. PMID: 36139378 Free PMC article.
Neuropathic pain in patients with Charcot-Marie-Tooth type 1A.
Bjelica B, Peric S, Basta I, Bozovic I, Kacar A, Marjanovic A, Ivanovic V, Brankovic M, Jankovic M, Novakovic I, Rakocevic Stojanovic V. Bjelica B, et al. Among authors: novakovic i. Neurol Sci. 2020 Mar;41(3):625-630. doi: 10.1007/s10072-019-04142-5. Epub 2019 Nov 15. Neurol Sci. 2020. PMID: 31729581
GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia.
Dobričić V, Tomić A, Branković V, Kresojević N, Janković M, Westenberger A, Rašić VM, Klein C, Novaković I, Svetel M, Kostić VS. Dobričić V, et al. Among authors: novakovic i. Parkinsonism Relat Disord. 2017 Dec;45:81-84. doi: 10.1016/j.parkreldis.2017.09.017. Epub 2017 Sep 18. Parkinsonism Relat Disord. 2017. PMID: 28958832
Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review.
Dawod PGA, Jancic J, Marjanovic A, Brankovic M, Jankovic M, Samardzic J, Gamil Anwar Dawod A, Novakovic I, Abdel Motaleb FI, Radlovic V, Kostic VS, Nikolic D. Dawod PGA, et al. Among authors: novakovic i. Diagnostics (Basel). 2021 Oct 23;11(11):1969. doi: 10.3390/diagnostics11111969. Diagnostics (Basel). 2021. PMID: 34829316 Free PMC article.
158 results