2nd Department of Neurology Comenius University in Bratislava Faculty of Medicine University Hospital Bratislava Bratislava Slovak Republic

Department of Clinical Neurosciences Scientific Park MEDIPARK P J Safarik University Kosice Slovak Republic

Department of Neurology 2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic

Department of Neurology and Centre of Clinical Neuroscience 1st Faculty of Medicine Charles University and General University Hospital Prague Prague Czech Republic

Department of Neurology and HUN REN PTE Clinical Neuroscience MR Research Group University of Pecs Medical School Pécs Hungary

Department of Neurology Comenius University and University Hospital Martin Martin Slovak Republic

Department of Neurology P J Safarik University Kosice Slovak Republic

Department of Neurology Semmelweis University Budapest Hungary

Department of Neurology Silesian Centre of Neurology Katowice Katowice Poland

Department of Neurology University Hospital of L Pasteur Kosice Slovak Republic

Department of Neurology University of Szeged Szeged Hungary

Department of Neurology Zvolen Hospital Zvolen Slovak Republic

Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology London UK

Institute of Normal and Pathological Physiology Centre of Experimental Medicine Slovak Academy of Sciences Bratislava Slovak Republic

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Skorvanek M, Rizig M, Athanasiou‐Fragkouli A, et al. PubMed DOI

Font‐Porterias N, Arauna LR, Poveda A, et al. European Roma groups show complex west Eurasian admixture footprints and a common south Asian genetic origin. PLoS Genet. 2019;15(9):e1008417. doi: 10.1371/journal.pgen.1008417 PubMed DOI PMC

Ostrozovicova M, Jech R, Steel D, et al. A recurrent VPS16 p.Arg187* nonsense variant in early‐onset generalized dystonia. Mov Disord. 2021;36(8):1984‐1985. doi: 10.1002/mds.28647 PubMed DOI

Skorvanek M, Rektorova I, Mandemakers W, et al. WARS2 mutations cause DOPA‐responsive early‐onset parkinsonism and progressive myoclonus ataxia. Parkinsonism Relat Disord. 2022;94:54‐61. doi: 10.1016/j.parkreldis.2021.11.030 PubMed DOI

Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's Disease

p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central Europe