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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 1
2006 6
2008 1
2009 4
2010 4
2011 4
2012 6
2013 11
2014 4
2015 13
2016 9
2017 5
2018 1
2019 9
2020 9
2021 12
2022 9
2023 11
2024 3

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107 results

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Page 1
Genetic Testing in Parkinson's Disease.
Pal G, Cook L, Schulze J, Verbrugge J, Alcalay RN, Merello M, Sue CM, Bardien S, Bonifati V, Chung SJ, Foroud T, Gatto E, Hall A, Hattori N, Lynch T, Marder K, Mascalzoni D, Novaković I, Thaler A, Raymond D, Salari M, Shalash A, Suchowersky O, Mencacci NE, Simuni T, Saunders-Pullman R, Klein C. Pal G, et al. Among authors: novakovic i. Mov Disord. 2023 Aug;38(8):1384-1396. doi: 10.1002/mds.29500. Epub 2023 Jun 27. Mov Disord. 2023. PMID: 37365908 Free PMC article.
Genetic and Epigenomic Modifiers of Diabetic Neuropathy.
Jankovic M, Novakovic I, Nikolic D, Mitrovic Maksic J, Brankovic S, Petronic I, Cirovic D, Ducic S, Grajic M, Bogicevic D. Jankovic M, et al. Among authors: novakovic i. Int J Mol Sci. 2021 May 5;22(9):4887. doi: 10.3390/ijms22094887. Int J Mol Sci. 2021. PMID: 34063061 Free PMC article. Review.
NBIA Syndromes: A Step Forward from the Previous Knowledge.
Svetel M, Dragašević N, Petrović I, Novaković I, Tomić A, Kresojević N, Stanković I, Kostić V. Svetel M, et al. Among authors: novakovic i. Neurol India. 2021 Sep-Oct;69(5):1380-1388. doi: 10.4103/0028-3886.329603. Neurol India. 2021. PMID: 34747818 Free article. Review.
Incidence of Syndromes Associated With Frontotemporal Lobar Degeneration in 9 European Countries.
Logroscino G, Piccininni M, Graff C, Hardiman O, Ludolph AC, Moreno F, Otto M, Remes AM, Rowe JB, Seelaar H, Solje E, Stefanova E, Traykov L, Jelic V, Rydell MT, Pender N, Anderl-Straub S, Barandiaran M, Gabilondo A, Krüger J, Murley AG, Rittman T, van der Ende EL, van Swieten JC, Hartikainen P, Stojmenovic GM, Mehrabian S, Benussi L, Alberici A, Dell'Abate MT, Zecca C, Borroni B; FRONTIERS group. Logroscino G, et al. JAMA Neurol. 2023 Mar 1;80(3):279-286. doi: 10.1001/jamaneurol.2022.5128. JAMA Neurol. 2023. PMID: 36716024 Free PMC article.
Novel GATOR1 variants in focal epilepsy.
Kovačević M, Janković M, Branković M, Milićević O, Novaković I, Sokić D, Ristić A, Shamsani J, Vojvodić N. Kovačević M, et al. Among authors: novakovic i. Epilepsy Behav. 2023 Apr;141:109139. doi: 10.1016/j.yebeh.2023.109139. Epub 2023 Feb 26. Epilepsy Behav. 2023. PMID: 36848747
International Genetic Testing and Counseling Practices for Parkinson's Disease.
Saunders-Pullman R, Raymond D, Ortega RA, Shalash A, Gatto E, Salari M, Markgraf M, Alcalay RN, Mascalzoni D, Mencacci NE, Bonifati V, Merello M, Chung SJ, Novakovic I, Bardien S, Pal G, Hall A, Hattori N, Lynch T, Thaler A, Sue CM, Foroud T, Verbrugge J, Schulze J, Cook L, Marder K, Suchowersky O, Klein C, Simuni T. Saunders-Pullman R, et al. Among authors: novakovic i. Mov Disord. 2023 Aug;38(8):1527-1535. doi: 10.1002/mds.29442. Epub 2023 Jun 13. Mov Disord. 2023. PMID: 37310233
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.
Genetic Aspects of Inflammation and Immune Response in Stroke.
Nikolic D, Jankovic M, Petrovic B, Novakovic I. Nikolic D, et al. Among authors: novakovic i. Int J Mol Sci. 2020 Oct 8;21(19):7409. doi: 10.3390/ijms21197409. Int J Mol Sci. 2020. PMID: 33049931 Free PMC article. Review.
Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
Perić S, Marković V, Candayan A, De Vriendt E, Momčilović N, Savić A, Dragašević-Mišković N, Svetel M, Stević Z, Božović I, Mesaroš Š, Drulović J, Basta I, Petrović I, Tamaš O, Mijajlović M, Novaković I, Sokić D, Jordanova A. Perić S, et al. Among authors: novakovic i. Cells. 2022 Sep 8;11(18):2804. doi: 10.3390/cells11182804. Cells. 2022. PMID: 36139378 Free PMC article.
107 results