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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.
The Lancet. Neurology|March 19, 2022
Prion protein monoclonal antibody (PRN100) therapy for Creutzfeldt-Jakob disease: evaluation of a first-in-human treatment programmeSimon Mead, Azadeh Khalili-Shirazi, Caroline Potter, et al.
Neuroimage. Clinical|November 18, 2019
Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian processLiane S Canas, Carole H Sudre, Enrico De Vita, 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.
Journal of Neurogenetics|January 10, 2025
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.
Journal of Neurology|March 29, 2025
PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Neurobiology of Disease|November 23, 2023
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6Emma Jones, Elizabeth Hill, Jacqueline Linehan, 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.
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