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Page 1
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
Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit.
Miletic A, Stojanovic JR, Parezanovic V, Rsovac S, Drakulic D, Soldatovic I, Mijovic M, Bosankic B, Petrovic H, Borlja N, Milivojevic M, Marjanovic A, Brankovic M, Cuturilo G. Miletic A, et al. Among authors: marjanovic a. Eur J Pediatr. 2021 Oct;180(10):3219-3227. doi: 10.1007/s00431-021-04097-w. Epub 2021 May 7. Eur J Pediatr. 2021. PMID: 33963417
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
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: marjanovic a. Diagnostics (Basel). 2021 Oct 23;11(11):1969. doi: 10.3390/diagnostics11111969. Diagnostics (Basel). 2021. PMID: 34829316 Free PMC article.
57 results