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Brain : a Journal of Neurology|February 28, 2012
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresColin J Mahoney, Jon Beck, Jonathan D Rohrer, et al.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.Journal of Alzheimer'S Disease : JAD|February 6, 2013
Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutationsRachael I Scahill, Gerard R Ridgway, Jonathan W Bartlett, et al.The Lancet. Neurology|October 26, 2016
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case seriesNatalie S Ryan, Jennifer M Nicholas, Philip S J Weston, et al.Human Brain Mapping|February 11, 2014
Profiles of white matter tract pathology in frontotemporal dementiaColin J Mahoney, Gerard R Ridgway, Ian B Malone, et al.Nature Genetics|October 16, 2012
A common single-nucleotide variant in T is strongly associated with chordomaNischalan Pillay, Vincent Plagnol, Patrick S Tarpey, et al.The Lancet. Neurology|February 20, 2021
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob diseasePeter Hermann, Brian Appleby, Jean-Philippe Brandel, et al.Neurology|July 13, 2026
Performance of Alzheimer Disease Plasma Biomarkers in Patients With Prion DiseasesThomas Coysh, Rhiannon Laban, Elena Veleva, et al.International Journal of Geriatric Psychiatry|December 20, 2019
Empowering Better End-of-Life Dementia Care (EMBED-Care): A mixed methods protocol to achieve integrated person-centred care across settingsElizabeth L Sampson, Janet E Anderson, Bridget Candy, et al.Pageof 22