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Genetic aspects of Alzheimer's disease.
Zekanowski C, Religa D, Graff C, Filipek S, Kuźnicki J. Zekanowski C, et al. Among authors: filipek s. 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. Among authors: filipek s. 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: filipek s. 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
A patient with posterior cortical atrophy possesses a novel mutation in the presenilin 1 gene.
Sitek EJ, Narożańska E, Pepłońska B, Filipek S, Barczak A, Styczyńska M, Mlynarczyk K, Brockhuis B, Portelius E, Religa D, Barcikowska M, Sławek J, Żekanowski C. Sitek EJ, et al. Among authors: filipek s. PLoS One. 2013 Apr 12;8(4):e61074. doi: 10.1371/journal.pone.0061074. Print 2013. PLoS One. 2013. PMID: 23593396 Free PMC article.
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: filipek s. PLoS One. 2014 Dec 26;9(12):e115470. doi: 10.1371/journal.pone.0115470. eCollection 2014. PLoS One. 2014. PMID: 25541946 Free PMC article.
134 results