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Human Molecular Genetics|March 13, 2018
Expression of C9orf72-related dipeptides impairs motor function in a vertebrate modelAmrutha Swaminathan, Marilou Bouffard, Meijiang Liao, et al.
Neurobiology of Aging|November 16, 2010
Analysis of optineurin in frontotemporal lobar degenerationSara Rollinson, Janis Bennion, Greg Toulson, et al.
Neurocase|September 11, 2008
Progressive anomia revisited: focal degeneration associated with progranulin gene mutationJulie S Snowden, Stuart M Pickering-Brown, Daniel Du Plessis, et al.
Acta Neuropathologica|May 29, 2008
TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degenerationPenelope Foulds, Erica McAuley, Linda Gibbons, et al.
Neurogenetics|April 15, 2009
Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degenerationRoberto Colombo, Daniela Tavian, Matthew C Baker, et al.
Neurobiology of Aging|December 2, 2014
Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degenerationLinda Gibbons, Sara Rollinson, Jennifer C Thompson, et al.
Brain : a Journal of Neurology|January 15, 2008
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutationsStuart M Pickering-Brown, Sara Rollinson, Daniel Du Plessis, et al.
Neurobiology of Aging|December 1, 2014
p62/SQSTM1 analysis in frontotemporal lobar degenerationLouise Miller, Sara Rollinson, Janis Bennion Callister, et al.
Neuroscience Letters|January 25, 2006
CHMP2B mutations are not a common cause of frontotemporal lobar degenerationAshley Cannon, Matthew Baker, Brad Boeve, et al.
Neurobiology of Aging|May 19, 2009
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degenerationSara Rollinson, Jonathan D Rohrer, Julie van der Zee, et al.
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