Romac S - Search Results

1

HD phenocopies--possible role of Saitohin gene.

Janković N, Kecmanović M, Dimitrijević R, Keckarević Marković M, Dobricić V, Keckarević D, Savić Pavicević D, Romac S. Janković N, et al. Among authors: romac s. Int J Neurosci. 2008 Mar;118(3):391-7. doi: 10.1080/00207450701593103. Int J Neurosci. 2008. PMID: 18300012

2

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

3

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

4

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

5

Human Y-specific STR haplotypes in population of Serbia and Montenegro.

Stevanović M, Dobricić V, Keckarević D, Perović A, Savić-Pavićević D, Keckarević-Marković M, Jovanović A, Romac S. Stevanović M, et al. Among authors: romac s. Forensic Sci Int. 2007 Sep 13;171(2-3):216-21. doi: 10.1016/j.forsciint.2006.05.038. Epub 2006 Jun 30. Forensic Sci Int. 2007. PMID: 16806776

6

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

7

Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients.

Keckarevic-Markovic M, Milic-Rasic V, Mladenovic J, Dackovic J, Kecmanovic M, Keckarevic D, Savic-Pavicevic D, Romac S. Keckarevic-Markovic M, et al. Among authors: romac s. J Peripher Nerv Syst. 2009 Jun;14(2):125-36. doi: 10.1111/j.1529-8027.2009.00222.x. J Peripher Nerv Syst. 2009. PMID: 19691535

8

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

9

Endothelial nitric oxide synthase gene polymorphisms and prostate cancer risk in Serbian population.

Branković A, Brajušković G, Nikolić Z, Vukotić V, Cerović S, Savić-Pavićević D, Romac S. Branković A, et al. Among authors: romac s. Int J Exp Pathol. 2013 Dec;94(6):355-61. doi: 10.1111/iep.12045. Epub 2013 Sep 2. Int J Exp Pathol. 2013. PMID: 23998439 Free PMC article.

10

The status of SCA1, MJD/SCA3, FRDA, DRPLA and MD triplet containing genes in patients with Huntington disease and healthy controls.

Keckarevic D, Culjkovic B, Savic D, Stojkovic O, Kostic V, Vukosavic S, Romac S. Keckarevic D, et al. Among authors: romac s. J Neurogenet. 2000 Dec;14(4):257-63. doi: 10.3109/01677060009084502. J Neurogenet. 2000. PMID: 11342385

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