Romac S - Search Results

1

Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history.

Savić D, Keckarević D, Branković-Srećković V, Apostolski S, Todorović S, Romac S. Savić D, et al. Among authors: romac s. Int J Neurosci. 2006 Dec;116(12):1509-18. doi: 10.1080/00207450600553182. Int J Neurosci. 2006. PMID: 17145685

2

250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.

Savić D, Rakocvic-Stojanovic V, Keckarevic D, Culjkovic B, Stojkovic O, Mladenovic J, Todorovic S, Apostolski S, Romac S. Savić D, et al. Among authors: romac s. Hum Mutat. 2002 Feb;19(2):131-9. doi: 10.1002/humu.10027. Hum Mutat. 2002. PMID: 11793472

3

Epidemiology of myotonic dystrophy type 1 (Steinert disease) in Belgrade (Serbia).

Mladenovic J, Pekmezovic T, Todorovic S, Rakocevic-Stojanovic V, Savic D, Romac S, Apostolski S. Mladenovic J, et al. Among authors: romac s. Clin Neurol Neurosurg. 2006 Dec;108(8):757-60. doi: 10.1016/j.clineuro.2006.04.004. Epub 2006 May 19. Clin Neurol Neurosurg. 2006. PMID: 16713671

4

A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from Serbia.

Kecmanović M, Ristić AJ, Ercegovac M, Keckarević-Marković M, Keckarević D, Sokić D, Romac S. Kecmanović M, et al. Among authors: romac s. Int J Neurosci. 2014 Feb;124(2):102-9. doi: 10.3109/00207454.2013.828723. Epub 2013 Sep 12. Int J Neurosci. 2014. PMID: 23883076

5

Haplotype analysis of the DM1 locus in the Serbian population.

Krndija D, Savić D, Mladenović J, Rakocević-Stojanović V, Apostolski S, Todorović S, Romac S. Krndija D, et al. Among authors: romac s. Acta Neurol Scand. 2005 Apr;111(4):274-7. doi: 10.1111/j.1600-0404.2005.00402.x. Acta Neurol Scand. 2005. PMID: 15740580

6

[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. Among authors: romac s. 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.

7

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

8

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: romac s. 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

9

Polymorphisms of the prion protein gene (PRNP) in a Serbian population.

Dimitrijević R, Cadez I, Keckarević-Marković M, Keckarević D, Kecmanović M, Dobricić V, Savić-Pavićević D, Brajusković G, Romac S. Dimitrijević R, et al. Among authors: romac s. Int J Neurosci. 2010 Jul;120(7):496-501. doi: 10.3109/00207451003765907. Int J Neurosci. 2010. PMID: 20583902

10

Schizophrenia and apolipoprotein E gene polymorphism in Serbian population.

Kecmanović M, Dobricić V, Dimitrijević R, Keckarević D, Savić-Pavićević D, Keckarević-Marković M, Ivkovic M, Romac S. Kecmanović M, et al. Among authors: romac s. Int J Neurosci. 2010 Jul;120(7):502-6. doi: 10.3109/00207451003765956. Int J Neurosci. 2010. PMID: 20583903

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