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Page 1
Clinical and Genetic Analysis of Psychosis in Parkinson's Disease.
Radojević B, Dragašević-Mišković NT, Marjanović A, Branković M, Dobričić V, Milovanović A, Tomić A, Svetel M, Petrović I, Jančić I, Stanisavljević D, Savić MM, Kostić VS. Radojević B, et al. Among authors: marjanovic a. J Parkinsons Dis. 2021;11(4):1973-1980. doi: 10.3233/JPD-212716. J Parkinsons Dis. 2021. PMID: 34151861
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: marjanovic a. 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: marjanovic a. Mov Disord. 2016 Jul;31(7):1071. doi: 10.1002/mds.26634. Epub 2016 May 4. Mov Disord. 2016. PMID: 27145302 No abstract available.
Five-year study of quality of life in myotonic dystrophy.
Peric S, Vujnic M, Dobricic V, Marjanovic A, Basta I, Novakovic I, Lavrnic D, Rakocevic-Stojanovic V. Peric S, et al. Among authors: marjanovic a. Acta Neurol Scand. 2016 Nov;134(5):346-351. doi: 10.1111/ane.12549. Epub 2015 Dec 21. Acta Neurol Scand. 2016. PMID: 27696366
Myotonic Dystrophy Type 2 - Data from the Serbian Registry.
Bozovic I, Peric S, Pesovic J, Bjelica B, Brkusanin M, Basta I, Bozic M, Sencanic I, Marjanovic A, Brankovic M, Savic-Pavicevic D, Rakocevic-Stojanovic V. Bozovic I, et al. Among authors: marjanovic a. J Neuromuscul Dis. 2018;5(4):461-469. doi: 10.3233/JND-180328. J Neuromuscul Dis. 2018. PMID: 30248060
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: marjanovic a. Neurol Sci. 2020 Mar;41(3):625-630. doi: 10.1007/s10072-019-04142-5. Epub 2019 Nov 15. Neurol Sci. 2020. PMID: 31729581
Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.
Peric S, Stevanovic J, Johnson K, Kosac A, Peric M, Brankovic M, Marjanovic A, Jankovic M, Banko B, Milenkovic S, Durdic M, Bozovic I, Glumac JN, Lavrnic D, Maksimovic R, Milic-Rasic V, Rakocevic-Stojanovic V. Peric S, et al. Among authors: marjanovic a. Acta Myol. 2019 Sep 1;38(3):163-171. eCollection 2019 Sep. Acta Myol. 2019. PMID: 31788660 Free PMC article.
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: marjanovic a. J Neurol. 2020 Dec;267(12):3617-3623. doi: 10.1007/s00415-020-10052-w. Epub 2020 Jul 8. J Neurol. 2020. PMID: 32642785
57 results