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Acta Neuropathologica|September 12, 2020
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt-Jakob diseaseLuke C Dabin, Fernando Guntoro, Tracy Campbell, et al.
Brain : a Journal of Neurology|August 23, 2006
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneitySimon Mead, Mark Poulter, Jon Beck, et al.
Brain : a Journal of Neurology|October 1, 2010
Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseasesDurrenajaf Siddique, Harpreet Hyare, Stephen Wroe, et al.
Brain : a Journal of Neurology|August 14, 2015
Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 yearsPeter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
Nature Communications|August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosisPenny J Norsworthy, Andrew G B Thompson, Tze H Mok, et al.
Plos Biology|June 10, 2020
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSSEmmanuel A Asante, Jacqueline M Linehan, Andrew Tomlinson, et al.
Nature|September 11, 2015
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyZane Jaunmuktane, Simon Mead, Matthew Ellis, et al.
Neuroimage. Clinical|December 13, 2016
Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry studyEnrico De Vita, Gerard R Ridgway, Mark J White, et al.
Alzheimer'S Research & Therapy|February 22, 2019
Longitudinal measurement of serum neurofilament light in presymptomatic familial Alzheimer's diseasePhilip S J Weston, Teresa Poole, Antoinette O'Connor, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2024
Huntington's disease phenocopy syndromes revisited: a clinical comparison and next-generation sequencing explorationCarolin Anna Maria Koriath, Fernando Guntoro, Penelope Norsworthy, et al.
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