Keckarević-Marković M - Search Results

1

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: keckarevic markovic m. 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

2

Coexistence of Unverricht-Lundborg disease and congenital deafness: molecular resolution of a complex comorbidity.

Kecmanović M, Ristić AJ, Sokić D, Keckarević-Marković M, Vojvodić N, Ercegovac M, Janković S, Keckarević D, Savić-Pavićević D, Romac S. Kecmanović M, et al. Epilepsia. 2009 Jun;50(6):1612-5. doi: 10.1111/j.1528-1167.2008.01937.x. Epub 2008 Dec 15. Epilepsia. 2009. PMID: 19170735 Free article.

3

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. Int J Neurosci. 2010 Jul;120(7):496-501. doi: 10.3109/00207451003765907. Int J Neurosci. 2010. PMID: 20583902

4

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. Int J Neurosci. 2010 Jul;120(7):502-6. doi: 10.3109/00207451003765956. Int J Neurosci. 2010. PMID: 20583903

5

An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth.

Keckarevic Markovic MP, Dackovic J, Mladenovic J, Milic-Rasic V, Kecmanovic M, Keckarevic D, Romac S. Keckarevic Markovic MP, et al. Genet Test Mol Biomarkers. 2013 Jan;17(1):85-7. doi: 10.1089/gtmb.2012.0238. Epub 2012 Nov 19. Genet Test Mol Biomarkers. 2013. PMID: 23163601 Free PMC article.

6

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. Int J Neurosci. 2008 Mar;118(3):391-7. doi: 10.1080/00207450701593103. Int J Neurosci. 2008. PMID: 18300012

7

Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin.

Kecmanović M, Jović N, Keckarević-Marković M, Keckarević D, Stevanović G, Ignjatović P, Romac S. Kecmanović M, et al. Among authors: keckarevic markovic m. Clin Genet. 2016 Jan;89(1):104-8. doi: 10.1111/cge.12570. Epub 2015 Mar 19. Clin Genet. 2016. PMID: 25683376

8

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. 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

9

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. 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

10

Lafora disease: severe phenotype associated with homozygous deletion of the NHLRC1 gene.

Kecmanović M, Jović N, Cukić M, Keckarević-Marković M, Keckarević D, Stevanović G, Romac S. Kecmanović M, et al. Among authors: keckarevic markovic m. J Neurol Sci. 2013 Feb 15;325(1-2):170-3. doi: 10.1016/j.jns.2012.12.006. Epub 2013 Jan 11. J Neurol Sci. 2013. PMID: 23317923 Review.

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