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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.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
October 14, 2008
Genetic susceptibility, evolution and the kuru epidemic
Simon Mead, Jerome Whitfield, Mark Poulter, et al.
Plos Genetics
|
February 14, 2009
HECTD2 is associated with susceptibility to mouse and human prion disease
Sarah E Lloyd, Emma G Maytham, Hirva Pota, et al.
Prion
|
September 30, 2025
Development of a user guide to support administration of the MRC Prion Disease Rating Scale in research and clinical settings for prion diseases
Robert S Pulido, Chris Marshall, Anne V Smith, 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.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 28, 2017
The TMEM106B risk allele is associated with lower cortical volumes in a clinically diagnosed frontotemporal dementia cohort
Sophie R Harding, Martina Bocchetta, Elizabeth Gordon, et al.
Nature Reviews. Neurology
|
November 10, 2020
Genetic testing in dementia - utility and clinical strategies
Carolin A M Koriath, Joanna Kenny, Natalie S Ryan, et al.
Blood
|
January 18, 2014
A highly specific blood test for vCJD
Graham S Jackson, Jesse Burk-Rafel, Julie A Edgeworth, et al.
American Journal of Human Genetics
|
March 20, 2024
Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemic
Liam Quinn, Jerome Whitfield, Michael P Alpers, et al.
Neurobiology of Aging
|
August 16, 2016
Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation
Jose Bras, Ruth Djaldetti, Ana Margarida Alves, et al.
Page
of 24
Search research articles
Search
Showing results (91-100 of 231) with videos related to
Sort By:
Page
of 24
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.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
October 14, 2008
Genetic susceptibility, evolution and the kuru epidemic
Simon Mead, Jerome Whitfield, Mark Poulter, et al.
Plos Genetics
|
February 14, 2009
HECTD2 is associated with susceptibility to mouse and human prion disease
Sarah E Lloyd, Emma G Maytham, Hirva Pota, et al.
Prion
|
September 30, 2025
Development of a user guide to support administration of the MRC Prion Disease Rating Scale in research and clinical settings for prion diseases
Robert S Pulido, Chris Marshall, Anne V Smith, 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.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 28, 2017
The TMEM106B risk allele is associated with lower cortical volumes in a clinically diagnosed frontotemporal dementia cohort
Sophie R Harding, Martina Bocchetta, Elizabeth Gordon, et al.
Nature Reviews. Neurology
|
November 10, 2020
Genetic testing in dementia - utility and clinical strategies
Carolin A M Koriath, Joanna Kenny, Natalie S Ryan, et al.
Blood
|
January 18, 2014
A highly specific blood test for vCJD
Graham S Jackson, Jesse Burk-Rafel, Julie A Edgeworth, et al.
American Journal of Human Genetics
|
March 20, 2024
Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemic
Liam Quinn, Jerome Whitfield, Michael P Alpers, et al.
Neurobiology of Aging
|
August 16, 2016
Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation
Jose Bras, Ruth Djaldetti, Ana Margarida Alves, et al.
Page
of 24