Svetel M - Search Results

1

Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations.

Kresojević N, Mijajlović M, Perić S, Pavlović A, Svetel M, Janković M, Dobričić V, Novaković I, Lakočević MB, Klein C, Kostić VS. Kresojević N, et al. Among authors: svetel m. Parkinsonism Relat Disord. 2013 Apr;19(4):431-5. doi: 10.1016/j.parkreldis.2012.12.006. Epub 2013 Jan 16. Parkinsonism Relat Disord. 2013. PMID: 23332636

2

[Clinico-pathomorphologic correlations in patients with symptomatic dystonias].

Ivanović N, Svetel M, Kozić D, Semnic R, Kostić V. Ivanović N, et al. Among authors: svetel m. Srp Arh Celok Lek. 2002 May-Jun;130(5-6):183-8. doi: 10.2298/sarh0206183i. Srp Arh Celok Lek. 2002. PMID: 12395440 Free article. Serbian.

3

Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia.

Müller B, Hedrich K, Kock N, Dragasevic N, Svetel M, Garrels J, Landt O, Nitschke M, Pramstaller PP, Reik W, Schwinger E, Sperner J, Ozelius L, Kostic V, Klein C. Müller B, et al. Among authors: svetel m. Am J Hum Genet. 2002 Dec;71(6):1303-11. doi: 10.1086/344531. Epub 2002 Nov 20. Am J Hum Genet. 2002. PMID: 12444570 Free PMC article.

4

Prevalence of primary late-onset focal dystonia in the Belgrade population.

Pekmezović T, Ivanović N, Svetel M, Nalić D, Smiljković T, Raicević R, Kostić VS. Pekmezović T, et al. Among authors: svetel m. Mov Disord. 2003 Nov;18(11):1389-92. doi: 10.1002/mds.10615. Mov Disord. 2003. PMID: 14639690

5

Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.

Djarmati A, Hedrich K, Svetel M, Schäfer N, Juric V, Vukosavic S, Hering R, Riess O, Romac S, Klein C, Kostic V. Djarmati A, et al. Among authors: svetel m. Hum Mutat. 2004 May;23(5):525. doi: 10.1002/humu.9240. Hum Mutat. 2004. PMID: 15108293

6

Bilateral chorea-ballism associated with hyperthyroidism.

Ristić AJ, Svetel M, Dragasević N, Zarković M, Koprivsek K, Kostić VS. Ristić AJ, et al. Among authors: svetel m. Mov Disord. 2004 Aug;19(8):982-3. doi: 10.1002/mds.20119. Mov Disord. 2004. PMID: 15300671

7

Incidence of vascular hemiballism in the population of Belgrade.

Pekmezović T, Svetel M, Ristić A, Raicević R, Ivanović N, Smiljković T, Kostić VS. Pekmezović T, et al. Among authors: svetel m. Mov Disord. 2004 Dec;19(12):1469-72. doi: 10.1002/mds.20256. Mov Disord. 2004. PMID: 15390051

8

Circulating and cerebrospinal fluid ghrelin and leptin: potential role in altered body weight in Huntington's disease.

Popovic V, Svetel M, Djurovic M, Petrovic S, Doknic M, Pekic S, Miljic D, Milic N, Glodic J, Dieguez C, Casanueva FF, Kostic V. Popovic V, et al. Among authors: svetel m. Eur J Endocrinol. 2004 Oct;151(4):451-5. doi: 10.1530/eje.0.1510451. Eur J Endocrinol. 2004. PMID: 15476444

9

Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin, and Jp-3 genes.

Keckarević M, Savić D, Svetel M, Kostić V, Vukosavić S, Romac S. Keckarević M, et al. Among authors: svetel m. Int J Neurosci. 2005 Feb;115(2):299-301. doi: 10.1080/00207450590519571. Int J Neurosci. 2005. PMID: 15764008

10

Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients.

Dragasević NT, Culjković B, Klein C, Ristić A, Keckarević M, Topisirović I, Vukosavić S, Svetel M, Kock N, Stefanova E, Romac S, Kostić VS. Dragasević NT, et al. Among authors: svetel m. Mov Disord. 2006 Feb;21(2):187-91. doi: 10.1002/mds.20687. Mov Disord. 2006. PMID: 16149098

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