Dragasević N - Search Results

1

Spinocerebellar ataxia type 17 in the Yugoslav population.

Alendar A, Euljković B, Savić D, Djarmati A, Keckarević M, Ristić A, Dragasević N, Kosić V, Romac S. Alendar A, et al. Among authors: dragasevic n. Acta Neurol Scand. 2004 Mar;109(3):185-7. doi: 10.1034/j.1600-0404.2003.00196.x. Acta Neurol Scand. 2004. PMID: 14763955

2

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. Mov Disord. 2006 Feb;21(2):187-91. doi: 10.1002/mds.20687. Mov Disord. 2006. PMID: 16149098

3

Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.

Topisirovic I, Dragasevic N, Savic D, Ristic A, Keckarevic M, Keckarevic D, Culjkovic B, Petrovic I, Romac S, Kostic VS. Topisirovic I, et al. Among authors: dragasevic n. Clin Genet. 2002 Oct;62(4):321-4. doi: 10.1034/j.1399-0004.2002.620412.x. Clin Genet. 2002. PMID: 12372061

4

SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism.

Svetel M, Djarmati A, Dragasević N, Savić D, Culjković B, Romac S, Kostić VS. Svetel M, et al. Among authors: dragasevic n. Eur J Neurol. 2003 Sep;10(5):597. doi: 10.1046/j.1468-1331.2003.00671.x. Eur J Neurol. 2003. PMID: 12940846

5

Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.

Weissbach A, Djarmati A, Klein C, Dragasević N, Zühlke C, Raković A, Guzvić M, Butz E, Tönnies H, Siebert R, Petrović I, Svetel M, Kostić VS, Lohmann K. Weissbach A, et al. Among authors: dragasevic n. Mov Disord. 2010 Aug 15;25(11):1577-82. doi: 10.1002/mds.22857. Mov Disord. 2010. PMID: 20589871

6

Survival of Huntington's disease patients in Serbia: longer survival in female patients.

Pekmezovic T, Svetel M, Maric J, Dujmovic-Basuroski I, Dragasevic N, Keckarevic M, Romac S, Kostic VS. Pekmezovic T, et al. Among authors: dragasevic n. Eur J Epidemiol. 2007;22(8):523-6. doi: 10.1007/s10654-007-9157-7. Epub 2007 Jul 25. Eur J Epidemiol. 2007. PMID: 17653603

7

Long-term prognosis of vascular hemiballismus.

Ristic A, Marinkovic J, Dragasevic N, Stanisavljevic D, Kostic V. Ristic A, et al. Among authors: dragasevic n. Stroke. 2002 Aug;33(8):2109-11. doi: 10.1161/01.str.0000022810.76115.c0. Stroke. 2002. PMID: 12154272

8

Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.

Stefanova E, Djarmati A, Momcilović D, Dragasević N, Svetel M, Klein C, Kostić VS. Stefanova E, et al. Among authors: dragasevic n. Mov Disord. 2006 Nov;21(11):2010-5. doi: 10.1002/mds.21095. Mov Disord. 2006. PMID: 16972263

9

Hereditary neuropathy with liability to pressure palsies associated with central nervous system myelin lesions.

Dacković J, Rakocević-Stojanović V, Pavlović S, Zamurović N, Dragasević N, Romac S, Apostolski S. Dacković J, et al. Among authors: dragasevic n. Eur J Neurol. 2001 Nov;8(6):689-92. doi: 10.1046/j.1468-1331.2001.00306.x. Eur J Neurol. 2001. PMID: 11784354

10

Bilateral chorea-ballism associated with hyperthyroidism.

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

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