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Preferences of residents and junior neurologists to attend conferences--an EAYNT survey.
J Neurol Sci. 2015 Oct 15;357(1-2):297-9. doi: 10.1016/j.jns.2015.06.060. Epub 2015 Jun 28.
J Neurol Sci. 2015.
PMID: 26145197
No abstract available.
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.
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International issues: an international survey of young neurologists' perceptions of future health care and neurology.
Macerollo A, Róna-Vörös K, Struhal W, Kobeleva X, Sellner J.
Macerollo A, et al. Among authors: rona voros k.
Neurology. 2015 Jan 27;84(4):e20-3. doi: 10.1212/WNL.0000000000001180.
Neurology. 2015.
PMID: 25628436
No abstract available.
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Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation.
Rona-Voros K, Eschbach J, Vernay A, Wiesner D, Schwalenstocker B, Geniquet P, Mousson De Camaret B, Echaniz-Laguna A, Loeffler JP, Ludolph AC, Weydt P, Dupuis L.
Rona-Voros K, et al.
Hum Mol Genet. 2013 Dec 20;22(25):5096-106. doi: 10.1093/hmg/ddt359. Epub 2013 Jul 29.
Hum Mol Genet. 2013.
PMID: 23900073
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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.
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The role of PGC-1α in the pathogenesis of neurodegenerative disorders.
Róna-Vörös K, Weydt P.
Róna-Vörös K, et al.
Curr Drug Targets. 2010 Oct;11(10):1262-9. doi: 10.2174/1389450111007011262.
Curr Drug Targets. 2010.
PMID: 20840068
Review.
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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.
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