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Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: genetic and bioinformatic assessment.
Zekanowski C, Golan MP, Krzyśko KA, Lipczyńska-Łojkowska W, Filipek S, Kowalska A, Rossa G, Pepłońska B, Styczyńska M, Maruszak A, Religa D, Wender M, Kulczycki J, Barcikowska M, Kuźnicki J. Zekanowski C, et al. Among authors: lipczynska lojkowska w. Exp Neurol. 2006 Jul;200(1):82-8. doi: 10.1016/j.expneurol.2006.01.022. Epub 2006 Mar 20. Exp Neurol. 2006. PMID: 16546171
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: lipczynska lojkowska w. 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
Paraoxonase activity and dementia.
Wehr H, Bednarska-Makaruk M, Graban A, Lipczyńska-Łojkowska W, Rodo M, Bochyńska A, Ryglewicz D. Wehr H, et al. Among authors: lipczynska lojkowska w. J Neurol Sci. 2009 Aug 15;283(1-2):107-8. doi: 10.1016/j.jns.2009.02.317. Epub 2009 Mar 5. J Neurol Sci. 2009. PMID: 19268306
25 results