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Page 1
A novel tau mutation, p.K317N, causes globular glial tauopathy.
Tacik P, DeTure M, Lin WL, Sanchez Contreras M, Wojtas A, Hinkle KM, Fujioka S, Baker MC, Walton RL, Carlomagno Y, Brown PH, Strongosky AJ, Kouri N, Murray ME, Petrucelli L, Josephs KA, Rademakers R, Ross OA, Wszolek ZK, Dickson DW. Tacik P, et al. Acta Neuropathol. 2015 Aug;130(2):199-214. doi: 10.1007/s00401-015-1425-0. Epub 2015 Apr 22. Acta Neuropathol. 2015. PMID: 25900293 Free PMC article.
Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy.
Tacik P, Sanchez-Contreras M, DeTure M, Murray ME, Rademakers R, Ross OA, Wszolek ZK, Parisi JE, Knopman DS, Petersen RC, Dickson DW. Tacik P, et al. Neuropathol Appl Neurobiol. 2017 Apr;43(3):200-214. doi: 10.1111/nan.12367. Epub 2017 Mar 8. Neuropathol Appl Neurobiol. 2017. PMID: 27859539 Free PMC article.
A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease.
Tacik P, DeTure M, Hinkle KM, Lin WL, Sanchez-Contreras M, Carlomagno Y, Pedraza O, Rademakers R, Ross OA, Wszolek ZK, Dickson DW. Tacik P, et al. J Neuropathol Exp Neurol. 2015 Nov;74(11):1042-52. doi: 10.1097/NEN.0000000000000248. J Neuropathol Exp Neurol. 2015. PMID: 26426266 Free PMC article.
FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G.
Tacik P, DeTure MA, Carlomagno Y, Lin WL, Murray ME, Baker MC, Josephs KA, Boeve BF, Wszolek ZK, Graff-Radford NR, Parisi JE, Petrucelli L, Rademakers R, Isaacson RS, Heilman KM, Petersen RC, Dickson DW, Kouri N. Tacik P, et al. Brain Pathol. 2017 Sep;27(5):612-626. doi: 10.1111/bpa.12428. Epub 2016 Oct 5. Brain Pathol. 2017. PMID: 27529406 Free PMC article.
[18F]AV-1451 tau-PET uptake does correlate with quantitatively measured 4R-tau burden in autopsy-confirmed corticobasal degeneration.
Josephs KA, Whitwell JL, Tacik P, Duffy JR, Senjem ML, Tosakulwong N, Jack CR, Lowe V, Dickson DW, Murray ME. Josephs KA, et al. Among authors: tacik p. Acta Neuropathol. 2016 Dec;132(6):931-933. doi: 10.1007/s00401-016-1618-1. Epub 2016 Sep 19. Acta Neuropathol. 2016. PMID: 27645292 Free PMC article. No abstract available.
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
Sanchez-Contreras M, Heckman MG, Tacik P, Diehl N, Brown PH, Soto-Ortolaza AI, Christopher EA, Walton RL, Ross OA, Golbe LI, Graff-Radford N, Wszolek ZK, Dickson DW, Rademakers R. Sanchez-Contreras M, et al. Among authors: tacik p. Mov Disord. 2017 Jan;32(1):115-123. doi: 10.1002/mds.26815. Epub 2016 Oct 6. Mov Disord. 2017. PMID: 27709685 Free PMC article.
Three sib-pairs of autopsy-confirmed progressive supranuclear palsy.
Fujioka S, Sanchez Contreras MY, Strongosky AJ, Ogaki K, Whaley NR, Tacik PM, van Gerpen JA, Uitti RJ, Ross OA, Wszolek ZK, Rademakers R, Dickson DW. Fujioka S, et al. Parkinsonism Relat Disord. 2015 Feb;21(2):101-5. doi: 10.1016/j.parkreldis.2014.10.028. Epub 2014 Nov 15. Parkinsonism Relat Disord. 2015. PMID: 25443551 Free PMC article.
Three families with Perry syndrome from distinct parts of the world.
Tacik P, Fiesel FC, Fujioka S, Ross OA, Pretelt F, Castañeda Cardona C, Kidd A, Hlavac M, Raizis A, Okun MS, Traynor S, Strongosky AJ, Springer W, Wszolek ZK. Tacik P, et al. Parkinsonism Relat Disord. 2014 Aug;20(8):884-8. doi: 10.1016/j.parkreldis.2014.05.004. Epub 2014 May 13. Parkinsonism Relat Disord. 2014. PMID: 24881494 Free PMC article.
54 results