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Year Number of Results
2011 19
2012 15
2013 10
2014 8
2015 4
2016 3
2017 1
2018 1
2024 0

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47 results

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Page 1
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
DeJesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, Nicholson AM, Finch NA, Flynn H, Adamson J, Kouri N, Wojtas A, Sengdy P, Hsiung GY, Karydas A, Seeley WW, Josephs KA, Coppola G, Geschwind DH, Wszolek ZK, Feldman H, Knopman DS, Petersen RC, Miller BL, Dickson DW, Boylan KB, Graff-Radford NR, Rademakers R. DeJesus-Hernandez M, et al. Neuron. 2011 Oct 20;72(2):245-56. doi: 10.1016/j.neuron.2011.09.011. Epub 2011 Sep 21. Neuron. 2011. PMID: 21944778 Free PMC article.
Frontotemporal dementia and its subtypes: a genome-wide association study.
Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Waldö ML, Nilsson K, Nilsson C, Mackenzie IR, Hsiung GY, Mann DM, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, Pastor P, Razquin C, Ortega-Cubero S, Alonso E, Perneczky R, Diehl-Schmid J, Alexopoulos P, Kurz A, Rainero I, Rubino E, Pinessi L, Rogaeva E, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JC, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Deschamps W, Van Langenhove T, Cruts M, Van Broeckhoven C, Cappa SF, Le Ber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Spillanti… See abstract for full author list ➔ Ferrari R, et al. Lancet Neurol. 2014 Jul;13(7):686-99. doi: 10.1016/S1474-4422(14)70065-1. Lancet Neurol. 2014. PMID: 24943344 Free PMC article.
Parkinson's disease: experimental models and reality.
Jiang P, Dickson DW. Jiang P, et al. Acta Neuropathol. 2018 Jan;135(1):13-32. doi: 10.1007/s00401-017-1788-5. Epub 2017 Nov 18. Acta Neuropathol. 2018. PMID: 29151169 Free PMC article. Review.
Familial progressive supranuclear palsy: a literature review.
Fujioka S, Van Gerpen JA, Uitti RJ, Dickson DW, Wszolek ZK. Fujioka S, et al. Neurodegener Dis. 2014;13(2-3):180-2. doi: 10.1159/000354975. Epub 2013 Sep 24. Neurodegener Dis. 2014. PMID: 24080486 Free article. Review.
Genetic susceptibility variants in parkinsonism.
Soto-Ortolaza AI, Ross OA. Soto-Ortolaza AI, et al. Parkinsonism Relat Disord. 2016 Jan;22 Suppl 1(0 1):S7-11. doi: 10.1016/j.parkreldis.2015.09.011. Epub 2015 Sep 7. Parkinsonism Relat Disord. 2016. PMID: 26414118 Free PMC article. Review.
Update on genetics of parkinsonism.
Fujioka S, Wszolek ZK. Fujioka S, et al. Neurodegener Dis. 2012;10(1-4):257-60. doi: 10.1159/000334285. Epub 2012 Jan 17. Neurodegener Dis. 2012. PMID: 22261420 Free PMC article. Review.
TDP-43 in aging and Alzheimer's disease - a review.
Wilson AC, Dugger BN, Dickson DW, Wang DS. Wilson AC, et al. Int J Clin Exp Pathol. 2011 Jan 30;4(2):147-55. Int J Clin Exp Pathol. 2011. PMID: 21326809 Free PMC article. Review.
VPS35 mutations in Parkinson disease.
Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, Conibear E, Wasserman WW, Aasly JO, Burkhard PR, Djaldetti R, Ghika J, Hentati F, Krygowska-Wajs A, Lynch T, Melamed E, Rajput A, Rajput AH, Solida A, Wu RM, Uitti RJ, Wszolek ZK, Vingerhoets F, Farrer MJ. Vilariño-Güell C, et al. Am J Hum Genet. 2011 Jul 15;89(1):162-7. doi: 10.1016/j.ajhg.2011.06.001. Am J Hum Genet. 2011. PMID: 21763482 Free PMC article.
47 results