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Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
Elert-Dobkowska E, Stepniak I, Krysa W, Rajkiewicz M, Rakowicz M, Sobanska A, Rudzinska M, Wasielewska A, Pilch J, Kubalska J, Lipczynska-Lojkowska W, Kulczycki J, Kurdziel K, Sikorska A, Beetz C, Zaremba J, Sulek A. Elert-Dobkowska E, et al. Among authors: rajkiewicz m. J Neurol Sci. 2015 Dec 15;359(1-2):35-9. doi: 10.1016/j.jns.2015.10.030. Epub 2015 Oct 17. J Neurol Sci. 2015. PMID: 26671083
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: rajkiewicz m. 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
WITHDRAWN: Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.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: rajkiewicz m. Neurol Neurochir Pol. 2018 May 17:S0028-3843(18)30152-X. doi: 10.1016/j.pjnns.2018.04.004. Online ahead of print. Neurol Neurochir Pol. 2018. PMID: 29880430 Free article.
Does quantitative EMG differ myotonic dystrophy type 2 and type 1?
Szmidt-Salkowska E, Gawel M, Lusakowska A, Nojszewska M, Lipowska M, Sulek A, Krysa W, Rajkiewicz M, Seroka A, Kaminska AM. Szmidt-Salkowska E, et al. Among authors: rajkiewicz m. J Electromyogr Kinesiol. 2014 Oct;24(5):755-61. doi: 10.1016/j.jelekin.2014.05.012. Epub 2014 Jun 25. J Electromyogr Kinesiol. 2014. PMID: 25052913
14 results