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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1992 1
1993 1
2003 2
2004 1
2005 4
2006 10
2007 17
2008 13
2009 10
2010 7
2011 1
2012 2
2014 2
2015 4
2016 3
2017 2
2018 3
2020 2
2021 3
2022 2
2023 2
2024 0

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Similar articles for PMID: 16979267

80 results

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Page 1
CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.
Cannon A, Baker M, Boeve B, Josephs K, Knopman D, Petersen R, Parisi J, Dickison D, Adamson J, Snowden J, Neary D, Mann D, Hutton M, Pickering-Brown SM. Cannon A, et al. Neurosci Lett. 2006 May 1;398(1-2):83-4. doi: 10.1016/j.neulet.2005.12.056. Epub 2006 Jan 23. Neurosci Lett. 2006. PMID: 16431024
No association of common VCP variants with sporadic frontotemporal dementia.
Schumacher A, Friedrich P, Diehl J, Ibach B, Schoepfer-Wendels A, Mueller JC, Konta L, Laws SM, Kurz A, Foerstl H, Riemenschneider M. Schumacher A, et al. Neurobiol Aging. 2009 Feb;30(2):333-5. doi: 10.1016/j.neurobiolaging.2007.05.023. Epub 2007 Jul 5. Neurobiol Aging. 2009. PMID: 17618707
Genetic analysis of MAPT haplotype diversity in frontotemporal dementia.
Laws SM, Friedrich P, Diehl-Schmid J, Müller J, Ibach B, Bäuml J, Eisele T, Förstl H, Kurz A, Riemenschneider M. Laws SM, et al. Neurobiol Aging. 2008 Aug;29(8):1276-8. doi: 10.1016/j.neurobiolaging.2007.02.019. Epub 2007 Mar 26. Neurobiol Aging. 2008. PMID: 17386961
The molecular basis of frontotemporal dementia.
Neumann M, Tolnay M, Mackenzie IR. Neumann M, et al. Expert Rev Mol Med. 2009 Jul 29;11:e23. doi: 10.1017/S1462399409001136. Expert Rev Mol Med. 2009. PMID: 19638255 Free article. Review.
Progranulin null mutations in both sporadic and familial frontotemporal dementia.
Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A; French Research Network on FTD/FTD-MND. Le Ber I, et al. Hum Mutat. 2007 Sep;28(9):846-55. doi: 10.1002/humu.20520. Hum Mutat. 2007. PMID: 17436289
TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3).
Rostgaard N, Roos P, Budtz-Jørgensen E, Johannsen P, Waldemar G, Nørremølle A, Lindquist SG, Gydesen S, Brown JM, Collinge J, Isaacs AM; FReJA collaboration; Nielsen TT, Nielsen JE. Rostgaard N, et al. Neurobiol Aging. 2017 Nov;59:221.e1-221.e7. doi: 10.1016/j.neurobiolaging.2017.06.026. Epub 2017 Jul 11. Neurobiol Aging. 2017. PMID: 28888721
80 results