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The Journal of Biological Chemistry|July 31, 2014
N-terminal domain of prion protein directs its oligomeric associationClare R Trevitt, Laszlo L P Hosszu, Mark Batchelor, 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.
Neurology|October 27, 2017
Serum neurofilament light in familial Alzheimer disease: A marker of early neurodegenerationPhilip S J Weston, Teresa Poole, Natalie S Ryan, et al.
Neurobiology of Aging|January 18, 2015
Small deletion in C9orf72 hides a proportion of expansion carriers in FTLDSara Rollinson, Janis Bennion Callister, Kate Young, et al.
Human Molecular Genetics|March 13, 2010
Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutationsHazel Urwin, Astrid Authier, Jorgen E Nielsen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
No evidence that extended tracts of homozygosity are associated with Alzheimer's diseaseRebecca Sims, Sarah Dwyer, Denise Harold, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|February 24, 2017
The clinical, neuroanatomical, and neuropathologic phenotype of TBK1-associated frontotemporal dementia: A longitudinal case reportCarolin A M Koriath, Martina Bocchetta, Emilie Brotherhood, et al.
Acta Neuropathologica|April 2, 2020
Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizooticO Noel Gill, Yvonne Spencer, Angela Richard-Loendt, et al.
Acta Neuropathologica|December 20, 2019
PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteinsGrant T Corbett, Zemin Wang, Wei Hong, et al.
Human Molecular Genetics|January 18, 2017
Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutationEmma L Clayton, Renzo Mancuso, Troels Tolstrup Nielsen, et al.
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