Novaković I - Search Results

1

Pharmacogenetics of drug response in Parkinson's disease.

Džoljić E, Novaković I, Krajinovic M, Grbatinić I, Kostić V. Džoljić E, et al. Among authors: novakovic i. Int J Neurosci. 2015;125(9):635-44. doi: 10.3109/00207454.2014.963851. Epub 2014 Oct 15. Int J Neurosci. 2015. PMID: 25226559 Review.

2

Homocysteine serum levels and MTHFR C677T genotype in patients with Parkinson's disease, with and without levodopa therapy.

Todorović Z, Dzoljić E, Novaković I, Mirković D, Stojanović R, Nesić Z, Krajinović M, Prostran M, Kostić V. Todorović Z, et al. Among authors: novakovic i. J Neurol Sci. 2006 Oct 25;248(1-2):56-61. doi: 10.1016/j.jns.2006.05.040. Epub 2006 Jun 13. J Neurol Sci. 2006. PMID: 16774768 Clinical Trial.

3

Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification.

Kostić VS, Lukić-Ječmenica M, Novaković I, Dobričić V, Brajković L, Krajinović M, Klein C, Pavlović A. Kostić VS, et al. Among authors: novakovic i. J Neurol. 2011 Sep;258(9):1637-42. doi: 10.1007/s00415-011-5985-1. Epub 2011 Mar 16. J Neurol. 2011. PMID: 21409505

4

Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort.

Dobricic V, Stefanova E, Jankovic M, Gurunlian N, Novakovic I, Hardy J, Kostic V, Guerreiro R. Dobricic V, et al. Among authors: novakovic i. Neurobiol Aging. 2012 Jul;33(7):1481.e7-12. doi: 10.1016/j.neurobiolaging.2011.12.007. Epub 2012 Jan 4. Neurobiol Aging. 2012. PMID: 22221884

5

Association of dihydrofolate reductase (DHFR) -317AA genotype with poor response to methotrexate in patients with rheumatoid arthritis.

Milic V, Jekic B, Lukovic L, Bunjevacki V, Milasin J, Novakovic I, Damnjanovic T, Popovic B, Maksimovic N, Damjanov N, Radunovic G, Pejnovic N, Krajinovic M. Milic V, et al. Among authors: novakovic i. Clin Exp Rheumatol. 2012 Mar-Apr;30(2):178-83. Epub 2012 Apr 13. Clin Exp Rheumatol. 2012. PMID: 22324981

6

Epilepsy in a child with Wolf-Hirschhorn syndrome.

Mitić V, Cuturilo G, Novaković I, Dimitrijević N, Damnjanović T, Dimitrijević A, Dobricić V, Kostić V, Radlović N. Mitić V, et al. Among authors: novakovic i. Srp Arh Celok Lek. 2011 Nov-Dec;139(11-12):795-9. Srp Arh Celok Lek. 2011. PMID: 22338478 Free article.

7

Association of the TYMS 3G/3G genotype with poor response and GGH 354GG genotype with the bone marrow toxicity of the methotrexate in RA patients.

Jekic B, Lukovic L, Bunjevacki V, Milic V, Novakovic I, Damnjanovic T, Milasin J, Popovic B, Maksimovic N, Damjanov N, Radunovic G, Kovacevic L, Krajinovic M. Jekic B, et al. Among authors: novakovic i. Eur J Clin Pharmacol. 2013 Mar;69(3):377-83. doi: 10.1007/s00228-012-1341-3. Epub 2012 Jul 5. Eur J Clin Pharmacol. 2013. PMID: 22763757

8

Skin and sural nerve biopsies: ultrastructural findings in the first genetically confirmed cases of CADASIL in Serbia.

Lackovic V, Bajcetic M, Lackovic M, Novakovic I, Labudović Borović M, Pavlovic A, Zidverc-Trajkovic J, Dzolic E, Rovcanin B, Sternic N, Kostic V. Lackovic V, et al. Among authors: novakovic i. Ultrastruct Pathol. 2012 Oct;36(5):325-35. doi: 10.3109/01913123.2012.679352. Ultrastruct Pathol. 2012. PMID: 23025651

9

Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia.

Dobričić VS, Kresojević ND, Svetel MV, Janković MZ, Petrović IN, Tomić AD, Novaković IV, Kostić VS. Dobričić VS, et al. J Neurol. 2013 Apr;260(4):1037-42. doi: 10.1007/s00415-012-6753-6. Epub 2012 Nov 20. J Neurol. 2013. PMID: 23180184

10

Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations.

Kresojević N, Mijajlović M, Perić S, Pavlović A, Svetel M, Janković M, Dobričić V, Novaković I, Lakočević MB, Klein C, Kostić VS. Kresojević N, et al. Among authors: novakovic i. Parkinsonism Relat Disord. 2013 Apr;19(4):431-5. doi: 10.1016/j.parkreldis.2012.12.006. Epub 2013 Jan 16. Parkinsonism Relat Disord. 2013. PMID: 23332636

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