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Two desmin gene mutations associated with myofibrillar myopathies in Polish families.
Fichna JP, Karolczak J, Potulska-Chromik A, Miszta P, Berdynski M, Sikorska A, Filipek S, Redowicz MJ, Kaminska A, Zekanowski C. Fichna JP, et al. Among authors: zekanowski c. PLoS One. 2014 Dec 26;9(12):e115470. doi: 10.1371/journal.pone.0115470. eCollection 2014. PLoS One. 2014. PMID: 25541946 Free PMC article.
[RNA editing].
Zekanowski C. Zekanowski C. Postepy Biochem. 1992;38(4):156-63. Postepy Biochem. 1992. PMID: 1293594 Review. Polish. No abstract available.
Genetic aspects of Alzheimer's disease.
Zekanowski C, Religa D, Graff C, Filipek S, Kuźnicki J. Zekanowski C, et al. Acta Neurobiol Exp (Wars). 2004;64(1):19-31. doi: 10.55782/ane-2004-1488. Acta Neurobiol Exp (Wars). 2004. PMID: 15190677 Free article. Review.
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. 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
Early-onset Alzheimer's disease with a de novo mutation in the presenilin 1 gene.
Golan MP, Styczyńska M, Jóźwiak K, Walecki J, Maruszak A, Pniewski J, Lugiewicz R, Filipek S, Zekanowski C, Barcikowska M. Golan MP, et al. Among authors: zekanowski c. Exp Neurol. 2007 Dec;208(2):264-8. doi: 10.1016/j.expneurol.2007.08.016. Epub 2007 Sep 5. Exp Neurol. 2007. PMID: 17931627
PIN1 gene variants in Alzheimer's disease.
Maruszak A, Safranow K, Gustaw K, Kijanowska-Haładyna B, Jakubowska K, Olszewska M, Styczyńska M, Berdyński M, Tysarowski A, Chlubek D, Siedlecki J, Barcikowska M, Zekanowski C. Maruszak A, et al. Among authors: zekanowski c. BMC Med Genet. 2009 Nov 12;10:115. doi: 10.1186/1471-2350-10-115. BMC Med Genet. 2009. PMID: 19909517 Free PMC article.
Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).
Gabryelewicz T, Masellis M, Berdynski M, Bilbao JM, Rogaeva E, St George-Hyslop P, Barczak A, Czyzewski K, Barcikowska M, Wszolek Z, Black SE, Zekanowski C. Gabryelewicz T, et al. Among authors: zekanowski c. J Alzheimers Dis. 2010;22(4):1123-33. doi: 10.3233/JAD-2010-101413. J Alzheimers Dis. 2010. PMID: 20930269 Free PMC article.
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.
Berdyński M, Kuźma-Kozakiewicz M, Ricci C, Kubiszewska J, Millecamps S, Salachas F, Łusakowska A, Carrera P, Meininger V, Battistini S, Kwieciński H, Zekanowski C. Berdyński M, et al. Among authors: zekanowski c. Amyotroph Lateral Scler. 2012 Jan;13(1):132-6. doi: 10.3109/17482968.2011.600316. Epub 2011 Aug 30. Amyotroph Lateral Scler. 2012. PMID: 21877919
111 results