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Acta Neurologica Belgica|March 20, 2012
Are irreversible morphological [corrected] signs of portal hypertension in neurological form of Wilson's disease associated with treatment delay? A pilot studyD B Kozic, R Semnic, I Petrovic, et al.European Journal of Neurology|August 28, 2003
SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonismM Svetel, A Djarmati, N Dragasević, et al.Srpski Arhiv Za Celokupno Lekarstvo|September 29, 1999
[Clinico-genetic study of type I spinocerebelllar ataxia]M Svetel, B Culjković, N Sternić, et al.European Journal of Neurology|October 13, 2016
Transcranial sonography in dopa-responsive dystoniaM Svetel, A Tomić, M Mijajlović, et al.Journal of the Neurological Sciences|August 13, 2018
Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's diseaseM Z Jankovic, V Dobricic, N Kresojevic, et al.European Journal of Neurology|May 29, 2009
Long-term outcome in Serbian patients with Wilson diseaseM Svetel, T Pekmezović, I Petrović, et al.European Journal of Neurology|July 21, 2012
Glucocerebrosidase mutations in a Serbian Parkinson's disease populationK R Kumar, A Ramirez, A Göbel, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Genetic heterogeneity in ten families with myoclonus-dystoniaB Schüle, N Kock, M Svetel, et al.Neurology|February 12, 2004
Mutations in DYT1: extension of the phenotypic and mutational spectrumK Kabakci, K Hedrich, J C Leung, et al.Pageof 3