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The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene.
Snowden JS, Hu Q, Rollinson S, Halliwell N, Robinson A, Davidson YS, Momeni P, Baborie A, Griffiths TD, Jaros E, Perry RH, Richardson A, Pickering-Brown SM, Neary D, Mann DM. Snowden JS, et al. Among authors: richardson a. Acta Neuropathol. 2011 Jul;122(1):99-110. doi: 10.1007/s00401-011-0816-0. Epub 2011 Mar 20. Acta Neuropathol. 2011. PMID: 21424531
Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation.
Pickering-Brown S, Baker M, Bird T, Trojanowski J, Lee V, Morris H, Rossor M, Janssen JC, Neary D, Craufurd D, Richardson A, Snowden J, Hardy J, Mann D, Hutton M. Pickering-Brown S, et al. Among authors: richardson a. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):79-82. doi: 10.1002/ajmg.b.20083. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755449
The apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in males.
Srinivasan R, Davidson Y, Gibbons L, Payton A, Richardson AM, Varma A, Julien C, Stopford C, Thompson J, Horan MA, Pendleton N, Pickering-Brown SM, Neary D, Snowden JS, Mann DM. Srinivasan R, et al. Among authors: richardson am. J Neurol Neurosurg Psychiatry. 2006 Feb;77(2):154-8. doi: 10.1136/jnnp.2005.063966. J Neurol Neurosurg Psychiatry. 2006. PMID: 16421115 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: richardson a. Nature. 2006 Aug 24;442(7105):916-9. doi: 10.1038/nature05016. Epub 2006 Jul 16. Nature. 2006. PMID: 16862116
Inferring thought and action in motor neurone disease.
Gibbons ZC, Snowden JS, Thompson JC, Happé F, Richardson A, Neary D. Gibbons ZC, et al. Among authors: richardson a. Neuropsychologia. 2007 Mar 25;45(6):1196-207. doi: 10.1016/j.neuropsychologia.2006.10.008. Epub 2006 Nov 22. Neuropsychologia. 2007. PMID: 17118410
Cognitive phenotypes in Alzheimer's disease and genetic risk.
Snowden JS, Stopford CL, Julien CL, Thompson JC, Davidson Y, Gibbons L, Pritchard A, Lendon CL, Richardson AM, Varma A, Neary D, Mann D. Snowden JS, et al. Among authors: richardson am. Cortex. 2007 Oct;43(7):835-45. doi: 10.1016/s0010-9452(08)70683-x. Cortex. 2007. PMID: 17941342
3,391 results