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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: rademakers r. Neurocase. 2014;20(1):69-86. doi: 10.1080/13554794.2012.732087. Epub 2012 Nov 5. Neurocase. 2014. PMID: 23121543 Free PMC article.
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C, Snowden J, Adamson J, Sadovnick AD, Rollinson S, Cannon A, Dwosh E, Neary D, Melquist S, Richardson A, Dickson D, Berger Z, Eriksen J, Robinson T, Zehr C, Dickey CA, Crook R, McGowan E, Mann D, Boeve B, Feldman H, Hutton M. Baker M, et al. Among authors: rademakers r. Nature. 2006 Aug 24;442(7105):916-9. doi: 10.1038/nature05016. Epub 2006 Jul 16. Nature. 2006. PMID: 16862116
Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.
Boeve BF, Baker M, Dickson DW, Parisi JE, Giannini C, Josephs KA, Hutton M, Pickering-Brown SM, Rademakers R, Tang-Wai D, Jack CR Jr, Kantarci K, Shiung MM, Golde T, Smith GE, Geda YE, Knopman DS, Petersen RC. Boeve BF, et al. Among authors: rademakers r. Brain. 2006 Nov;129(Pt 11):3103-14. doi: 10.1093/brain/awl268. Epub 2006 Oct 9. Brain. 2006. PMID: 17030535
Pallidonigral TDP-43 pathology in Perry syndrome.
Wider C, Dickson DW, Stoessl AJ, Tsuboi Y, Chapon F, Gutmann L, Lechevalier B, Calne DB, Personett DA, Hulihan M, Kachergus J, Rademakers R, Baker MC, Grantier LL, Sujith OK, Brown L, Calne S, Farrer MJ, Wszolek ZK. Wider C, et al. Among authors: rademakers r. Parkinsonism Relat Disord. 2009 May;15(4):281-6. doi: 10.1016/j.parkreldis.2008.07.005. Epub 2008 Aug 23. Parkinsonism Relat Disord. 2009. PMID: 18723384 Free PMC article.
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN.
Whitwell JL, Jack CR Jr, Boeve BF, Senjem ML, Baker M, Rademakers R, Ivnik RJ, Knopman DS, Wszolek ZK, Petersen RC, Josephs KA. Whitwell JL, et al. Among authors: rademakers r. Neurology. 2009 Mar 3;72(9):813-20. doi: 10.1212/01.wnl.0000343851.46573.67. Neurology. 2009. PMID: 19255408 Free PMC article.
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease.
Jasinska-Myga B, Wider C, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Baker M, Rademakers R, Uitti RJ, Farrer MJ, Ross OA, Wszolek ZK. Jasinska-Myga B, et al. Among authors: rademakers r. Eur J Neurol. 2009 Aug;16(8):909-11. doi: 10.1111/j.1468-1331.2009.02621.x. Epub 2009 Mar 31. Eur J Neurol. 2009. PMID: 19473366
Psychometric evaluation of personality in a patient with FTDP-17.
Sitek EJ, Narozańska E, Sławek J, Wójcik J, Wieczorek D, Robowski P, Schinwelski M, Jasińska-Myga B, Baker M, Rademakers R, Wszołek ZK. Sitek EJ, et al. Among authors: rademakers r. Psychiatry Clin Neurosci. 2010 Apr;64(2):211-2. doi: 10.1111/j.1440-1819.2009.02056.x. Psychiatry Clin Neurosci. 2010. PMID: 20447016 Free article. No abstract available.
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: rademakers r. 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.
504 results