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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: barcikowska 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: barcikowska m. Neurocase. 2014;20(1):69-86. doi: 10.1080/13554794.2012.732087. Epub 2012 Nov 5. Neurocase. 2014. PMID: 23121543 Free PMC article.
Association between Cerebrospinal Fluid Biomarkers for Alzheimer's Disease, APOE Genotypes and Auditory Verbal Learning Task in Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer's Disease.
Mandecka M, Budziszewska M, Barczak A, Pepłońska B, Chodakowska-Żebrowska M, Filipek-Gliszczyńska A, Nesteruk M, Styczyńska M, Barcikowska M, Gabryelewicz T. Mandecka M, et al. Among authors: barcikowska m. J Alzheimers Dis. 2016 Jul 29;54(1):157-68. doi: 10.3233/JAD-160176. J Alzheimers Dis. 2016. PMID: 27472875
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: barcikowska 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
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: barcikowska 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.
PARK2 variability in Polish Parkinson's disease patients--interaction with mitochondrial haplogroups.
Gaweda-Walerych K, Safranow K, Jasinska-Myga B, Bialecka M, Klodowska-Duda G, Rudzinska M, Czyzewski K, Cobb SA, Slawek J, Styczynska M, Opala G, Drozdzik M, Nishioka K, Farrer MJ, Ross OA, Wszolek ZK, Barcikowska M, Zekanowski C. Gaweda-Walerych K, et al. Among authors: barcikowska m. Parkinsonism Relat Disord. 2012 Jun;18(5):520-4. doi: 10.1016/j.parkreldis.2012.01.021. Epub 2012 Feb 22. Parkinsonism Relat Disord. 2012. PMID: 22361577 Free PMC article.
TOMM40 and APOE common genetic variants are not Parkinson's disease risk factors.
Peplonska B, Safranow K, Gaweda-Walerych K, Maruszak A, Czyzewski K, Rudzinska M, Barcikowska M, Zekanowski C. Peplonska B, et al. Among authors: barcikowska m. Neurobiol Aging. 2013 Aug;34(8):2078.e1-2. doi: 10.1016/j.neurobiolaging.2013.02.018. Epub 2013 Mar 21. Neurobiol Aging. 2013. PMID: 23522842
167 results