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Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2022
Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenonGargi Banerjee, Kiran Samra, Matthew E Adams, et al.Brain Communications|September 21, 2020
Putaminal diffusion tensor imaging measures predict disease severity across human prion diseasesHarpreet Hyare, Enrico De Vita, Marie-Claire Porter, et al.The Lancet. Neurology|January 24, 2026
Genetic causes and modifiers of prion diseasesSimon Mead, Peter Hermann, Tze How Mok, et al.British Medical Bulletin|October 3, 2003
Molecular and clinical classification of human prion diseaseJonathan D F Wadsworth, Andrew F Hill, Jonathan A Beck, et al.Transfusion|February 26, 2010
Discrimination between prion-infected and normal blood samples by protein misfolding cyclic amplificationM Howard Tattum, Samantha Jones, Suvankar Pal, et al.Neurogenetics|October 2, 2009
A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouseSarah E Lloyd, Emma G Maytham, Julia Grizenkova, et al.Nature|January 5, 2017
Structural variation in amyloid-β fibrils from Alzheimer's disease clinical subtypesWei Qiang, Wai-Ming Yau, Jun-Xia Lu, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 11, 2008
Alterations in Ca2+-buffering in prion-null mice: association with reduced afterhyperpolarizations in CA1 hippocampal neuronsAndrew D Powell, Emil C Toescu, John Collinge, et al.Plos One|March 11, 2020
Citizen science improves our understanding of the impact of soil management on wild pollinator abundance in agroecosystemsLogan R Appenfeller, Sarah Lloyd, Zsofia SzendreiNeurology|July 13, 2026
Performance of Alzheimer Disease Plasma Biomarkers in Patients With Prion DiseasesThomas Coysh, Rhiannon Laban, Elena Veleva, et al.Pageof 43