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Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.Molecular Cell|May 1, 2007
Disease-associated prion protein oligomers inhibit the 26S proteasomeMark Kristiansen, Pelagia Deriziotis, Derek E Dimcheff, et al.Communications Biology|July 31, 2020
Structural effects of the highly protective V127 polymorphism on human prion proteinLaszlo L P Hosszu, Rebecca Conners, Daljit Sangar, et al.Brain : a Journal of Neurology|February 28, 2012
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic miceShabnam Ghazi-Noori, Kristina E Froud, Sarah Mizielinska, et al.Alzheimer'S Research & Therapy|September 26, 2012
Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansionsColin J Mahoney, Laura E Downey, Gerard R Ridgway, et al.Neurology|December 24, 2013
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopiesDavina J Hensman Moss, Mark Poulter, Jon Beck, et al.Emerging Infectious Diseases|April 22, 2015
Recent US Case of Variant Creutzfeldt-Jakob Disease-Global ImplicationsAtul Maheshwari, Michael Fischer, Pierluigi Gambetti, et al.Neurobiology of Aging|March 2, 2021
A novel presenilin 1 duplication mutation (Ile168dup) causing Alzheimer's disease associated with myoclonus, seizures and pyramidal featuresAntoinette O'Connor, Emily Abel, M R Fraser, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2018
Plasma tau is increased in frontotemporal dementiaMartha S Foiani, Ione Oc Woollacott, Carolin Heller, et al.Viruses|September 28, 2021
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat InsertionNicholas Brennecke, Ignazio Cali, Tze How Mok, et al.Pageof 36