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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: 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
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
Pathological correlates of frontotemporal lobar degeneration in the elderly.
Baborie A, Griffiths TD, Jaros E, McKeith IG, Burn DJ, Richardson A, Ferrari R, Moreno J, Momeni P, Duplessis D, Pal P, Rollinson S, Pickering-Brown S, Thompson JC, Neary D, Snowden JS, Perry R, Mann DM. Baborie A, et al. Among authors: rollinson s. Acta Neuropathol. 2011 Mar;121(3):365-71. doi: 10.1007/s00401-010-0765-z. Epub 2010 Oct 27. Acta Neuropathol. 2011. PMID: 20978901
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
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.
Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease.
Rollinson S, Halliwell N, Young K, Callister JB, Toulson G, Gibbons L, Davidson YS, Robinson AC, Gerhard A, Richardson A, Neary D, Snowden J, Mann DM, Pickering-Brown SM. Rollinson S, et al. Neurobiol Aging. 2012 Aug;33(8):1846.e5-6. doi: 10.1016/j.neurobiolaging.2012.01.109. Epub 2012 Mar 10. Neurobiol Aging. 2012. PMID: 22410647
Frontotemporal dementia with amyotrophic lateral sclerosis: a clinical comparison of patients with and without repeat expansions in C9orf72.
Snowden JS, Harris J, Richardson A, Rollinson S, Thompson JC, Neary D, Mann DM, Pickering-Brown S. Snowden JS, et al. Among authors: rollinson s. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Apr;14(3):172-6. doi: 10.3109/21678421.2013.765485. Epub 2013 Feb 19. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23421625
103 results