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Page 1
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: berdynski m. J Alzheimers Dis. 2010;22(4):1123-33. doi: 10.3233/JAD-2010-101413. J Alzheimers Dis. 2010. PMID: 20930269 Free PMC article.
Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?
Sitek EJ, Narozanska E, Barczak A, Jasinska-Myga B, Harciarek M, Chodakowska-Zebrowska M, Kubiak M, Wieczorek D, Konieczna S, Rademakers R, Baker M, Berdynski M, Brockhuis B, Barcikowska M, Zekanowski C, Heilman KM, Wszolek ZK, Slawek J. Sitek EJ, et al. Among authors: berdynski m. Neurocase. 2014;20(1):69-86. doi: 10.1080/13554794.2012.732087. Epub 2012 Nov 5. Neurocase. 2014. PMID: 23121543 Free PMC article.
Overactive BRCA1 Affects Presenilin 1 in Induced Pluripotent Stem Cell-Derived Neurons in Alzheimer's Disease.
Wezyk M, Szybinska A, Wojsiat J, Szczerba M, Day K, Ronnholm H, Kele M, Berdynski M, Peplonska B, Fichna JP, Ilkowski J, Styczynska M, Barczak A, Zboch M, Filipek-Gliszczynska A, Bojakowski K, Skrzypczak M, Ginalski K, Kabza M, Makalowska I, Barcikowska-Kotowicz M, Wojda U, Falk A, Zekanowski C. Wezyk M, et al. Among authors: berdynski m. J Alzheimers Dis. 2018;62(1):175-202. doi: 10.3233/JAD-170830. J Alzheimers Dis. 2018. PMID: 29439343
TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients.
Peplonska B, Berdynski M, Mandecka M, Barczak A, Kuzma-Kozakiewicz M, Barcikowska M, Zekanowski C. Peplonska B, et al. Among authors: berdynski m. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):407-412. doi: 10.1080/21678421.2018.1451894. Epub 2018 Mar 20. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29557178
TREM2 Gene Compound Heterozygosity in Neurodegenerative Disorders.
Berdyński M, Ludwiczak J, Barczak A, Barcikowska-Kotowicz M, Kuźma-Kozakiewicz M, Dunin-Horkawicz S, Żekanowski C, Borzemska B. Berdyński M, et al. J Alzheimers Dis. 2022;89(4):1211-1219. doi: 10.3233/JAD-220210. J Alzheimers Dis. 2022. PMID: 36031890
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: berdynski m. BMC Med Genet. 2009 Nov 12;10:115. doi: 10.1186/1471-2350-10-115. BMC Med Genet. 2009. PMID: 19909517 Free PMC article.
29 results