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New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background.
Bartoníková T, Menšíková K, Kolaříková K, Vodička R, Vrtěl R, Otruba P, Kaiserová M, Vaštík M, Mikulicová L, Ovečka J, Šáchová L, Dvorský F, Krša J, Jugas P, Godava M, Bareš M, Janout V, Hluštík P, Procházka M, Kaňovský P. Bartoníková T, et al. Medicine (Baltimore). 2018 Sep;97(38):e12313. doi: 10.1097/MD.0000000000012313. Medicine (Baltimore). 2018. PMID: 30235682 Free PMC article.
Familial, autosomal-dominant neurodegenerative parkinsonism with cognitive deterioration spanning five generations in a genetically isolated population of south-eastern Moravia, Czech Republic.
Mensikova K, Godava M, Kanovsky P, Otruba P, Kaiserova M, Vastik M, Mikulicova L, Bartonikova T, Vrtel R, Vodicka R, Kurcova S, Jugas P, Ovecka J, Sachova L, Dvorsky F. Mensikova K, et al. Among authors: bartonikova t. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Mar;160(1):158-60. doi: 10.5507/bp.2015.013. Epub 2015 Apr 15. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016. PMID: 25877408 Free article.
Atypical parkinsonism of progressive supranuclear palsy-parkinsonism (PSP-P) phenotype with rare variants in FBXO7 and VPS35 genes associated with Lewy body pathology.
Menšíková K, Tučková L, Kolařiková K, Bartoníková T, Vodička R, Ehrmann J, Vrtěl R, Procházka M, Kaňovský P, Kovacs GG. Menšíková K, et al. Among authors: bartonikova t. Acta Neuropathol. 2019 Jan;137(1):171-173. doi: 10.1007/s00401-018-1923-y. Epub 2018 Oct 29. Acta Neuropathol. 2019. PMID: 30374525 No abstract available.