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[Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
Rakowicz M, Zdzienicka E, Poniatowska R, Waliniowska E, Sułek A, Jakubowska T, Niedzielska K, Rola R, Wierzbicka A, Hoffman-Zacharska D, Głazowski C, Jakubczyk T, Niewiadomska M, Zaremba J. Rakowicz M, et al. Among authors: zaremba j. Neurol Neurochir Pol. 2005 Jul-Aug;39(4):263-275. Neurol Neurochir Pol. 2005. PMID: 16096942 Polish.
[Familial occurrence of FXTAS caused by premutation in the FMR1 gene].
Koziorowski D, Rajkiewicz M, Sułek-Piątkowska A, Zaremba J, Kaca-Oryńska M, Mandat T, Friedman A. Koziorowski D, et al. Among authors: zaremba j. Neurol Neurochir Pol. 2011 Jul-Aug;45(4):391-8. doi: 10.1016/s0028-3843(14)60111-0. Neurol Neurochir Pol. 2011. PMID: 22102001 Polish.
Hereditary form of prion disease in Poland.
Zimowski J, Kulczycki J, Lojkowska W, Szpak G, Krysa W, Szirkowiec W, Limon-Sztencel A, Zaremba J. Zimowski J, et al. Among authors: zaremba j. Neurol Neurochir Pol. 2012 Nov-Dec;46(6):509-18. doi: 10.5114/ninp.2012.32353. Neurol Neurochir Pol. 2012. PMID: 23319218
Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.
Sulek A, Lusakowska A, Krysa W, Rajkiewicz M, Kaminska A, Nojszewska M, Kostera-Pruszczyk A, Zdzienicka E, Kubalska J, Rakowicz M, Szirkowiec W, Kwiecinski H, Zaremba J. Sulek A, et al. Among authors: zaremba j. Neurol Neurochir Pol. 2018 Nov-Dec;52(6):736-742. doi: 10.1016/j.pjnns.2018.02.008. Epub 2018 Mar 7. Neurol Neurochir Pol. 2018. PMID: 29588063
[Clinical and genetic study of juvenile form of Huntington's disease].
Zdzienicka E, Rakowicz M, Mierzewska H, Hoffman-Zacharska D, Jakubowska T, Poniatowska R, Sułek A, Waliniowska E, Zalewska U, Kulczycki J, Zaremba J. Zdzienicka E, et al. Among authors: zaremba j. Neurol Neurochir Pol. 2002 Mar-Apr;36(2):245-58. Neurol Neurochir Pol. 2002. PMID: 12046502 Polish.
203 results