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Page 1
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: svetel m. J Psychosom Res. 2024 Dec;187:111911. doi: 10.1016/j.jpsychores.2024.111911. Epub 2024 Sep 1. J Psychosom Res. 2024. PMID: 39244967
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways.
Magrinelli F, Tesson C, Angelova PR, Salazar-Villacorta A, Rodriguez JA, Scardamaglia A, Chung BH, Jaconelli M, Vona B, Esteras N, Kwong AK, Courtin T, Maroofian R, Alavi S, Nirujogi R, Severino M, Lewis PA, Efthymiou S, O'Callaghan B, Buchert R, Sofan L, Lis P, Pinon C, Breedveld GJ, Chui MM, Murphy D, Pitz V, Makarious MB, Cassar M, Hassan BA, Iftikhar S, Rocca C, Bauer P, Tinazzi M, Svetel M, Samanci B, Hanağası HA, Bilgiç B, Obeso JA, Kurtis MM, Cogan G, Başak AN, Kiziltan G, Gül T, Yalçın G, Elibol B, Barišić N, Ng EW, Fan SS, Hershkovitz T, Weiss K, Raza Alvi J, Sultan T, Azmi Alkhawaja I, Froukh T, E Alrukban HA, Fauth C, Schatz UA, Zöggeler T, Zech M, Stals K, Varghese V, Gandhi S, Blauwendraat C, Hardy JA, Lesage S, Bonifati V, Haack TB, Bertoli-Avella AM, Steinfeld R, Alessi DR, Steller H, Brice A, Abramov AY, Bhatia KP, Houlden H. Magrinelli F, et al. Among authors: svetel m. medRxiv [Preprint]. 2024 Jun 20:2024.06.19.24308302. doi: 10.1101/2024.06.19.24308302. medRxiv. 2024. PMID: 39148840 Free PMC article. Preprint.
Early Screening for the Parkinson Variant of Multiple System Atrophy: A 6-Item Score.
Fanciulli A, Stankovic I, Avraham O, Jecmenica Lukic M, Ezra A, Leys F, Goebel G, Krismer F, Petrovic I, Svetel M, Seppi K, Kostic V, Giladi N, Poewe W, Wenning GK, Gurevich T. Fanciulli A, et al. Among authors: svetel m. Mov Disord Clin Pract. 2024 Apr 24;11(7):867-73. doi: 10.1002/mdc3.14048. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 38659282 Free PMC article.
Genotype-phenotype correlation in PRKN-associated Parkinson's disease.
Menon PJ, Sambin S, Criniere-Boizet B, Courtin T, Tesson C, Casse F, Ferrien M, Mariani LL, Carvalho S, Lejeune FX, Rebbah S, Martet G, Houot M, Lanore A, Mangone G, Roze E, Vidailhet M, Aasly J, Gan Or Z, Yu E, Dauvilliers Y, Zimprich A, Tomantschger V, Pirker W, Álvarez I, Pastor P, Di Fonzo A, Bhatia KP, Magrinelli F, Houlden H, Real R, Quattrone A, Limousin P, Korlipara P, Foltynie T, Grosset D, Williams N, Narendra D, Lin HP, Jovanovic C, Svetel M, Lynch T, Gallagher A, Vandenberghe W, Gasser T, Brockmann K, Morris HR, Borsche M, Klein C, Corti O, Brice A, Lesage S, Corvol JC; French Parkinson disease Genetics Study Group (PDG). Menon PJ, et al. Among authors: svetel m. NPJ Parkinsons Dis. 2024 Mar 29;10(1):72. doi: 10.1038/s41531-024-00677-3. NPJ Parkinsons Dis. 2024. PMID: 38553467 Free PMC article.
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: svetel m. Neurogenetics. 2024 Jul;25(3):165-177. doi: 10.1007/s10048-024-00755-x. Epub 2024 Mar 19. Neurogenetics. 2024. PMID: 38499745
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia.
Milovanović A, Dragaševic-Mišković N, Thomsen M, Borsche M, Hinrichs F, Westenberger A, Klein C, Brüggemann N, Branković M, Marjanović A, Svetel M, Kostić VS, Lohmann K. Milovanović A, et al. Among authors: svetel m. Mov Disord Clin Pract. 2024 Jun;11(6):626-633. doi: 10.1002/mdc3.14020. Epub 2024 Mar 15. Mov Disord Clin Pract. 2024. PMID: 38487929 Free PMC article.
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series.
Milovanović A, Westenberger A, Stanković I, Tamaš O, Branković M, Marjanović A, Laabs BH, Brand M, Rajalingam R, Marras C, Lohmann K, Branković V, Novaković I, Petrović I, Svetel M, Klein C, Kostić VS, Dragašević-Mišković N. Milovanović A, et al. Among authors: svetel m. Mov Disord. 2024 May;39(5):887-892. doi: 10.1002/mds.29729. Epub 2024 Mar 12. Mov Disord. 2024. PMID: 38469933
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: svetel m. 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.
167 results