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103 results

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Page 1
p62/SQSTM1 analysis in frontotemporal lobar degeneration.
Miller L, Rollinson S, Callister JB, Young K, Harris J, Gerhard A, Neary D, Richardson A, Snowden J, Mann DM, Pickering-Brown SM. Miller L, et al. Among authors: rollinson s. Neurobiol Aging. 2015 Mar;36(3):1603.e5-9. doi: 10.1016/j.neurobiolaging.2014.08.035. Epub 2014 Oct 18. Neurobiol Aging. 2015. PMID: 25433461
TDP-43 gene analysis in frontotemporal lobar degeneration.
Rollinson S, Snowden JS, Neary D, Morrison KE, Mann DM, Pickering-Brown SM. Rollinson S, et al. Neurosci Lett. 2007 May 23;419(1):1-4. doi: 10.1016/j.neulet.2007.03.044. Epub 2007 Mar 24. Neurosci Lett. 2007. PMID: 17434264
The genetics of frontotemporal lobar degeneration.
Sikkink S, Rollinson S, Pickering-Brown SM. Sikkink S, et al. Among authors: rollinson s. Curr Opin Neurol. 2007 Dec;20(6):693-8. doi: 10.1097/WCO.0b013e3282f1c961. Curr Opin Neurol. 2007. PMID: 17992091 Review.
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.
Pickering-Brown SM, Rollinson S, Du Plessis D, Morrison KE, Varma A, Richardson AM, Neary D, Snowden JS, Mann DM. Pickering-Brown SM, et al. Among authors: rollinson s. Brain. 2008 Mar;131(Pt 3):721-31. doi: 10.1093/brain/awm331. Epub 2008 Jan 11. Brain. 2008. PMID: 18192287
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration.
Rollinson S, Rizzu P, Sikkink S, Baker M, Halliwell N, Snowden J, Traynor BJ, Ruano D, Cairns N, Rohrer JD, Mead S, Collinge J, Rossor M, Akay E, Guerreiro R, Rademakers R, Morrison KE, Pastor P, Alonso E, Martinez-Lage P, Graff-Radford N, Neary D, Heutink P, Mann DM, Van Swieten J, Pickering-Brown SM. Rollinson S, et al. Neurobiol Aging. 2009 Apr;30(4):656-65. doi: 10.1016/j.neurobiolaging.2009.01.009. Epub 2009 Feb 12. Neurobiol Aging. 2009. PMID: 19217189 Free PMC article.
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration.
Rollinson S, Rohrer JD, van der Zee J, Sleegers K, Mead S, Engelborghs S, Collinge J, De Deyn PP, Mann DM, Van Broeckhoven C, Pickering-Brown SM. Rollinson S, et al. Neurobiol Aging. 2011 Apr;32(4):754-5. doi: 10.1016/j.neurobiolaging.2009.04.009. Epub 2009 May 14. Neurobiol Aging. 2011. PMID: 19446372
Analysis of optineurin in frontotemporal lobar degeneration.
Rollinson S, Bennion J, Toulson G, Halliwell N, Usher S, Snowden J, Richardson A, Neary D, Mann D, Pickering-Brown SM. Rollinson S, et al. Neurobiol Aging. 2012 Feb;33(2):425.e1-2. doi: 10.1016/j.neurobiolaging.2010.10.002. Epub 2010 Nov 12. Neurobiol Aging. 2012. PMID: 21074902
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: rollinson s. Acta Neuropathol. 2011 Jul;122(1):99-110. doi: 10.1007/s00401-011-0816-0. Epub 2011 Mar 20. Acta Neuropathol. 2011. PMID: 21424531
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations.
Snowden JS, Rollinson S, Thompson JC, Harris JM, Stopford CL, Richardson AM, Jones M, Gerhard A, Davidson YS, Robinson A, Gibbons L, Hu Q, DuPlessis D, Neary D, Mann DM, Pickering-Brown SM. Snowden JS, et al. Among authors: rollinson s. Brain. 2012 Mar;135(Pt 3):693-708. doi: 10.1093/brain/awr355. Epub 2012 Feb 2. Brain. 2012. PMID: 22300873 Free PMC article.
103 results