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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: barczak a. PLoS One. 2013 Apr 12;8(4):e61074. doi: 10.1371/journal.pone.0061074. Print 2013. PLoS One. 2013. PMID: 23593396 Free PMC article.
Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland.
Zekanowski C, Styczyńska M, Pepłońska B, Gabryelewicz T, Religa D, Ilkowski J, Kijanowska-Haładyna B, Kotapka-Minc S, Mikkelsen S, Pfeffer A, Barczak A, Łuczywek E, Wasiak B, Chodakowska-Zebrowska M, Gustaw K, Łaczkowski J, Sobów T, Kuźnicki J, Barcikowska M. Zekanowski C, et al. Among authors: barczak a. Exp Neurol. 2003 Dec;184(2):991-6. doi: 10.1016/S0014-4886(03)00384-4. Exp Neurol. 2003. PMID: 14769392
The E318G substitution in PSEN1 gene is not connected with Alzheimer's disease in a large Polish cohort.
Zekanowski C, Pepłońska B, Styczyńska M, Religa D, Pfeffer A, Czyzewski K, Gabryelewicz T, Szybińska A, Kijanowska-Haładyna B, Kotapka-Minc S, Łuczywek E, Barczak A, Wasiak B, Chodakowska-Zebrowska M, Przekop I, Kuźnicki J, Barcikowska M. Zekanowski C, et al. Among authors: barczak a. Neurosci Lett. 2004 Mar 11;357(3):167-70. doi: 10.1016/j.neulet.2003.12.052. Neurosci Lett. 2004. PMID: 15003276
Neurocognition of centenarians: neuropsychological study of élite centenarians.
Luczywek E, Gabryelewicz T, Barczak A, Religa D, Pfeffer A, Styczynska M, Peplonska B, Chodakowska-Zebrowska M, Barcikowska M. Luczywek E, et al. Among authors: barczak a. Int J Geriatr Psychiatry. 2007 Oct;22(10):1004-8. doi: 10.1002/gps.1780. Int J Geriatr Psychiatry. 2007. PMID: 17431928
Prediction of deterioration of mild cognitive impairment with CT and SPECT.
Gabryelewicz T, Pawłowska-Detko A, Miśko J, Cwikła JB, Pfeffer A, Barczak A, Wasiak B, Łuczywek E, Królicki L, Walecki J, Barcikowska M. Gabryelewicz T, et al. Among authors: barczak a. Med Sci Monit. 2007 May;13 Suppl 1:31-7. Med Sci Monit. 2007. PMID: 17507882
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: barczak a. J Alzheimers Dis. 2010;22(4):1123-33. doi: 10.3233/JAD-2010-101413. J Alzheimers Dis. 2010. PMID: 20930269 Free PMC article.
141 results