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Lancet (London, England)
|
February 8, 2011
Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay
Julie Ann Edgeworth, Michael Farmer, Anita Sicilia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 13, 2022
Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease
Akin Nihat, Tze How Mok, Hans Odd, et al.
Acta Neuropathologica Communications
|
November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases
Lilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.
Dementia and Geriatric Cognitive Disorders Extra
|
September 11, 2012
Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1
Christopher Carswell, Michael Rañopa, Suvankar Pal, et al.
Annals of Clinical and Translational Neurology
|
May 23, 2015
The cognitive profile of prion disease: a prospective clinical and imaging study
Diana Caine, Renata J Tinelli, Harpreet Hyare, et al.
Acta Neuropathologica
|
May 28, 2021
Alzheimer's disease neuropathological change three decades after iatrogenic amyloid-β transmission
Zane Jaunmuktane, Gargi Banerjee, Simon Paine, et al.
The New England Journal of Medicine
|
January 19, 2017
Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129
Tzehow Mok, Zane Jaunmuktane, Susan Joiner, et al.
Brain : a Journal of Neurology
|
April 4, 2013
The Medical Research Council prion disease rating scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies
Andrew G B Thompson, Jessica Lowe, Zoe Fox, et al.
Brain : a Journal of Neurology
|
October 1, 2010
Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases
Durrenajaf 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 years
Peter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
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of 7
Search research articles
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Showing results (41-50 of 66) with videos related to
Sort By:
Page
of 7
Lancet (London, England)
|
February 8, 2011
Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay
Julie Ann Edgeworth, Michael Farmer, Anita Sicilia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 13, 2022
Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease
Akin Nihat, Tze How Mok, Hans Odd, et al.
Acta Neuropathologica Communications
|
November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases
Lilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.
Dementia and Geriatric Cognitive Disorders Extra
|
September 11, 2012
Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1
Christopher Carswell, Michael Rañopa, Suvankar Pal, et al.
Annals of Clinical and Translational Neurology
|
May 23, 2015
The cognitive profile of prion disease: a prospective clinical and imaging study
Diana Caine, Renata J Tinelli, Harpreet Hyare, et al.
Acta Neuropathologica
|
May 28, 2021
Alzheimer's disease neuropathological change three decades after iatrogenic amyloid-β transmission
Zane Jaunmuktane, Gargi Banerjee, Simon Paine, et al.
The New England Journal of Medicine
|
January 19, 2017
Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129
Tzehow Mok, Zane Jaunmuktane, Susan Joiner, et al.
Brain : a Journal of Neurology
|
April 4, 2013
The Medical Research Council prion disease rating scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies
Andrew G B Thompson, Jessica Lowe, Zoe Fox, et al.
Brain : a Journal of Neurology
|
October 1, 2010
Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases
Durrenajaf 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 years
Peter Rudge, Zane Jaunmuktane, Peter Adlard, et al.
Page
of 7