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Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.
Pottier C, Bieniek KF, Finch N, van de Vorst M, Baker M, Perkersen R, Brown P, Ravenscroft T, van Blitterswijk M, Nicholson AM, DeTure M, Knopman DS, Josephs KA, Parisi JE, Petersen RC, Boylan KB, Boeve BF, Graff-Radford NR, Veltman JA, Gilissen C, Murray ME, Dickson DW, Rademakers R. Pottier C, et al. Among authors: parisi je. Acta Neuropathol. 2015 Jul;130(1):77-92. doi: 10.1007/s00401-015-1436-x. Epub 2015 May 6. Acta Neuropathol. 2015. PMID: 25943890 Free PMC article.
Rapidly progressive aphasic dementia and motor neuron disease.
Caselli RJ, Windebank AJ, Petersen RC, Komori T, Parisi JE, Okazaki H, Kokmen E, Iverson R, Dinapoli RP, Graff-Radford NR, et al. Caselli RJ, et al. Among authors: parisi je. Ann Neurol. 1993 Feb;33(2):200-7. doi: 10.1002/ana.410330210. Ann Neurol. 1993. PMID: 8257465
A kinematic study of progressive apraxia with and without dementia.
Caselli RJ, Stelmach GE, Caviness JN, Timmann D, Royer T, Boeve BF, Parisi JE. Caselli RJ, et al. Among authors: parisi je. Mov Disord. 1999 Mar;14(2):276-87. doi: 10.1002/1531-8257(199903)14:2<276::aid-mds1013>3.0.co;2-u. Mov Disord. 1999. PMID: 10091622
470 results