Keckarevic M - Search Results

1

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: keckarevic m. 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

2

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. Int J Neurosci. 2005 Feb;115(2):299-301. doi: 10.1080/00207450590519571. Int J Neurosci. 2005. PMID: 15764008

3

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

4

JP-3 gene polymorphism in a healthy population of Serbia and Montenegro.

Keckarević M, Savić D, Romac S. Keckarević M, et al. J Genet. 2005 Apr;84(1):69-71. doi: 10.1007/BF02715892. J Genet. 2005. PMID: 15876586

5

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: keckarevic m. Clin Genet. 2002 Oct;62(4):321-4. doi: 10.1034/j.1399-0004.2002.620412.x. Clin Genet. 2002. PMID: 12372061

6

Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data).

Keckarević D, Savić D, Keckarević M, Stevanović M, Tarasjev A, Culjković B, Darmati A, Vukosavić S, Romac S. Keckarević D, et al. Among authors: keckarevic m. Forensic Sci Int. 2005 Jul 16;151(2-3):315-6. doi: 10.1016/j.forsciint.2005.01.009. Forensic Sci Int. 2005. PMID: 15939169

7

[Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients] ].

Keckarević M, Savić D, Culjković B, Zamurović N, Major T, Keckarević D, Todorović S, Romac S. Keckarević M, et al. Srp Arh Celok Lek. 2002 May-Jun;130(5-6):154-8. doi: 10.2298/sarh0206154k. Srp Arh Celok Lek. 2002. PMID: 12395434 Free article. Serbian.

8

Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?

Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S. Savić D, et al. Among authors: keckarevic m. Psychiatr Genet. 2001 Dec;11(4):201-5. doi: 10.1097/00041444-200112000-00004. Psychiatr Genet. 2001. PMID: 11807410

9

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: keckarevic m. Acta Neurol Scand. 2004 Mar;109(3):185-7. doi: 10.1034/j.1600-0404.2003.00196.x. Acta Neurol Scand. 2004. PMID: 14763955

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