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The clinical manifestations of two novel SPAST mutations.
Zádori D, Máté A, Róna-Vörös K, Gergev G, Zimmermann A, Nagy N, Széll M, Vécsei L, Sztriha L, Klivényi P. Zádori D, et al. Among authors: rona voros k. Clin Neurol Neurosurg. 2015 Sep;136:82-5. doi: 10.1016/j.clineuro.2015.05.009. Epub 2015 Jun 6. Clin Neurol Neurosurg. 2015. PMID: 26086985 No abstract available.
E-learning preferences of European junior neurologists-an EAYNT survey.
Sztriha LK, Varga ET, Róna-Vörös K, Holler N, Ilea R, Kobeleva X, Falup-Pecurariu C, Struhal W, Sellner J. Sztriha LK, et al. Among authors: rona voros k. Front Neurol. 2012 Dec 4;3:167. doi: 10.3389/fneur.2012.00167. eCollection 2012. Front Neurol. 2012. PMID: 23316182 Free PMC article. No abstract available.
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons.
Braunstein KE, Eschbach J, Ròna-Vörös K, Soylu R, Mikrouli E, Larmet Y, René F, Gonzalez De Aguilar JL, Loeffler JP, Müller HP, Bucher S, Kaulisch T, Niessen HG, Tillmanns J, Fischer K, Schwalenstöcker B, Kassubek J, Pichler B, Stiller D, Petersen A, Ludolph AC, Dupuis L. Braunstein KE, et al. Among authors: rona voros k. Hum Mol Genet. 2010 Nov 15;19(22):4385-98. doi: 10.1093/hmg/ddq361. Epub 2010 Aug 31. Hum Mol Genet. 2010. PMID: 20807776 Free PMC article.