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Whole exome sequencing in Serbian patients with hereditary spastic paraplegia.
Neurogenetics. 2024 Mar 19. doi: 10.1007/s10048-024-00755-x. Online ahead of print.
Neurogenetics. 2024.
PMID: 38499745
Clinical score for early diagnosis of myotonic dystrophy type 2.
Ivanovic V, Peric S, Pesovic J, Tubic R, Bozovic I, Petrovic Djordjevic I, Savic-Pavicevic D, Meola G, Rakocevic-Stojanovic V.
Ivanovic V, et al. Among authors: tubic r.
Neurol Sci. 2023 Mar;44(3):1059-1067. doi: 10.1007/s10072-022-06507-9. Epub 2022 Nov 19.
Neurol Sci. 2023.
PMID: 36401657
Free PMC article.
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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: tubic r.
J Neurol. 2020 Dec;267(12):3617-3623. doi: 10.1007/s00415-020-10052-w. Epub 2020 Jul 8.
J Neurol. 2020.
PMID: 32642785
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