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Neurology|April 3, 2016
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromesIan T S Coyle-Gilchrist, Katrina M Dick, Karalyn Patterson, et al.Proceedings of the National Academy of Sciences of the United States of America|September 9, 2020
Highly infectious prions are not directly neurotoxicIryna Benilova, Madeleine Reilly, Cassandra Terry, et al.Journal of Molecular Biology|February 21, 2021
Brazilin Removes Toxic Alpha-Synuclein and Seeding Competent Assemblies from Parkinson Brain by Altering Conformational EquilibriumGeorge R Nahass, Yuanzi Sun, Yong Xu, et al.Proceedings of the National Academy of Sciences of the United States of America|September 30, 2010
Pharmacological chaperone for the structured domain of human prion proteinAndrew J Nicoll, Clare R Trevitt, M Howard Tattum, et al.The Lancet. Neurology|September 19, 2020
Potential human transmission of amyloid β pathology: surveillance and risksElsa Lauwers, Giovanna Lalli, Sebastian Brandner, et al.Nature Communications|September 12, 2013
Amyloid-β nanotubes are associated with prion protein-dependent synaptotoxicityAndrew J Nicoll, Silvia Panico, Darragh B Freir, et al.The Lancet. Neurology|February 2, 2015
C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosisJonathan D Rohrer, Adrian M Isaacs, Sarah Mizielinska, et al.Neuroimage|August 15, 2009
Progressive logopenic/phonological aphasia: erosion of the language networkJonathan D Rohrer, Gerard R Ridgway, Sebastian J Crutch, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 14, 2014
Altered body schema processing in frontotemporal dementia with C9ORF72 mutationsLaura E Downey, Phillip D Fletcher, Hannah L Golden, et al.Acta Neuropathologica|September 12, 2015
Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathologyEmma L Clayton, Sarah Mizielinska, James R Edgar, et al.Pageof 36