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Mutations in DYT1: extension of the phenotypic and mutational spectrum.
Kabakci K, Hedrich K, Leung JC, Mitterer M, Vieregge P, Lencer R, Hagenah J, Garrels J, Witt K, Klostermann F, Svetel M, Friedman J, Kostic V, Bressman SB, Breakefield XO, Ozelius LJ, Pramstaller PP, Klein C. Kabakci K, et al. Among authors: svetel m. Neurology. 2004 Feb 10;62(3):395-400. doi: 10.1212/01.wnl.0000113024.84178.f7. Neurology. 2004. PMID: 14872019
Genetic heterogeneity in ten families with myoclonus-dystonia.
Schüle B, Kock N, Svetel M, Dragasevic N, Hedrich K, De Carvalho Aguiar P, Liu L, Kabakci K, Garrels J, Meyer EM, Berisavac I, Schwinger E, Kramer PL, Ozelius LJ, Klein C, Kostic V. Schüle B, et al. Among authors: svetel m. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1181-5. doi: 10.1136/jnnp.2003.027177. J Neurol Neurosurg Psychiatry. 2004. PMID: 15258227 Free PMC article.
Glucocerebrosidase mutations in a Serbian Parkinson's disease population.
Kumar KR, Ramirez A, Göbel A, Kresojević N, Svetel M, Lohmann K, M Sue C, Rolfs A, Mazzulli JR, Alcalay RN, Krainc D, Klein C, Kostic V, Grünewald A. Kumar KR, et al. Among authors: svetel m, m sue c. Eur J Neurol. 2013 Feb;20(2):402-5. doi: 10.1111/j.1468-1331.2012.03817.x. Epub 2012 Jul 20. Eur J Neurol. 2013. PMID: 22812582
Transcranial sonography in dopa-responsive dystonia.
Svetel M, Tomić A, Mijajlović M, Dobričić V, Novaković I, Pekmezović T, Brajković L, Kostić VS. Svetel M, et al. Eur J Neurol. 2017 Jan;24(1):161-166. doi: 10.1111/ene.13172. Epub 2016 Oct 12. Eur J Neurol. 2017. PMID: 27731537
Paroxysmal hemiballism and idiopathic hypoparathyroidism.
Dragasević N, Petković-Medved B, Svetel M, Filipović SR, Kostić VS. Dragasević N, et al. Among authors: svetel m. J Neurol. 1997 Jun;244(6):389-90. doi: 10.1007/s004150050108. J Neurol. 1997. PMID: 9249626 No abstract available.
167 results