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Page 1
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.
Vollstedt EJ, Madoev H, Aasly A, Ahmad-Annuar A, Al-Mubarak B, Alcalay RN, Alvarez V, Amorin I, Annesi G, Arkadir D, Bardien S, Barker RA, Barkhuizen M, Basak AN, Bonifati V, Boon A, Brighina L, Brockmann K, Carmine Belin A, Carr J, Clarimon J, Cornejo-Olivas M, Correia Guedes L, Corvol JC, Crosiers D, Damásio J, Das P, de Carvalho Aguiar P, De Rosa A, Dorszewska J, Ertan S, Ferese R, Ferreira J, Gatto E, Genç G, Giladi N, Gómez-Garre P, Hanagasi H, Hattori N, Hentati F, Hoffman-Zacharska D, Illarioshkin SN, Jankovic J, Jesús S, Kaasinen V, Kievit A, Klivenyi P, Kostic V, Koziorowski D, Kühn AA, Lang AE, Lim SY, Lin CH, Lohmann K, Markovic V, Martikainen MH, Mellick G, Merello M, Milanowski L, Mir P, Öztop-Çakmak Ö, Pimentel MMG, Pulkes T, Puschmann A, Rogaeva E, Sammler EM, Skaalum Petersen M, Skorvanek M, Spitz M, Suchowersky O, Tan AH, Termsarasab P, Thaler A, Tumas V, Valente EM, van de Warrenburg B, Williams-Gray CH, Wu RM, Zhang B, Zimprich A, Solle J, Padmanabhan S, Klein C. Vollstedt EJ, et al. Among authors: markovic v. PLoS One. 2023 Oct 3;18(10):e0292180. doi: 10.1371/journal.pone.0292180. eCollection 2023. PLoS One. 2023. PMID: 37788254 Free PMC article.
MRI biomarkers of freezing of gait development in Parkinson's disease.
Sarasso E, Basaia S, Cividini C, Stojkovic T, Stankovic I, Piramide N, Tomic A, Markovic V, Stefanova E, Kostic VS, Filippi M, Agosta F. Sarasso E, et al. Among authors: markovic v. NPJ Parkinsons Dis. 2022 Nov 15;8(1):158. doi: 10.1038/s41531-022-00426-4. NPJ Parkinsons Dis. 2022. PMID: 36379944 Free PMC article.
Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism".
Kresojević N, Marković V, Dobričić V, Stanković I, Stojković T, Tomić A, Lukić MJ, Janković M, Marjanović A, Branković M, Novaković I, Petrović I, Dragašević N, Svetel M, Kostić V. Kresojević N, et al. Among authors: markovic v. Mov Disord. 2023 Apr;38(4):712-713. doi: 10.1002/mds.29351. Mov Disord. 2023. PMID: 37061878 No abstract available.
Clinical and Genetic Features of Huntington's Disease Patients From Republic of Serbia: A Single-Center Experience.
Kresojević N, Perović I, Stanković I, Tomić A, Lukic MJ, Marković V, Stojković T, Mandić G, Janković M, Marjanović A, Branković M, Novaković I, Petrović I, Dragašević N, Stefanova E, Svetel M, Kostić V. Kresojević N, et al. Among authors: markovic v. J Mov Disord. 2023 Sep;16(3):333-335. doi: 10.14802/jmd.23028. Epub 2023 Jun 9. J Mov Disord. 2023. PMID: 37749975 Free PMC article. No abstract available.
Motor imagery ability in patients with functional dystonia.
Tomić A, Ječmenica Lukić M, Petrović I, Korkut V, Kresojević N, Marković V, Dragašević Mišković N, Svetel M, Kostić VS. Tomić A, et al. Among authors: markovic v. J Psychosom Res. 2024 Dec;187:111911. doi: 10.1016/j.jpsychores.2024.111911. Epub 2024 Sep 1. J Psychosom Res. 2024. PMID: 39244967
Whole exome sequencing in Serbian patients with hereditary spastic paraplegia.
Brankovic M, Ivanovic V, Basta I, Khang R, Lee E, Stevic Z, Ralic B, Tubic R, Seo G, Markovic V, Bozovic I, Svetel M, Marjanovic A, Veselinovic N, Mesaros S, Jankovic M, Savic-Pavicevic D, Jovin Z, Novakovic I, Lee H, Peric S. Brankovic M, et al. Among authors: markovic v. Neurogenetics. 2024 Jul;25(3):165-177. doi: 10.1007/s10048-024-00755-x. Epub 2024 Mar 19. Neurogenetics. 2024. PMID: 38499745
309 results