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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: brockhuis b. Neurocase. 2014;20(1):69-86. doi: 10.1080/13554794.2012.732087. Epub 2012 Nov 5. Neurocase. 2014. PMID: 23121543 Free PMC article.
Frontotemporal dementia and parkinsonism linked to chromosome 17--the first Polish family.
Narożańska E, Jasińska-Myga B, Sitek EJ, Robowski P, Brockhuis B, Lass P, Dubaniewicz M, Wieczorek D, Baker M, Rademakers R, Wszolek ZK, Sławek J. Narożańska E, et al. Among authors: brockhuis b. Eur J Neurol. 2011 Mar;18(3):535-7. doi: 10.1111/j.1468-1331.2010.03107.x. Eur J Neurol. 2011. PMID: 20561037 Free PMC article.
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: brockhuis b. PLoS One. 2013 Apr 12;8(4):e61074. doi: 10.1371/journal.pone.0061074. Print 2013. PLoS One. 2013. PMID: 23593396 Free PMC article.
23 results