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Simon Mead

Showing results (41-50 of 231) with videos related to

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Nature Reviews. Disease Primers|February 29, 2024
Creutzfeldt-Jakob disease and other prion diseasesInga Zerr, Anna Ladogana, Simon Mead, et al.
Acta Neuropathologica|May 18, 2010
Tau, prions and Aβ: the triad of neurodegenerationLilla Reiniger, Ana Lukic, Jacqueline Linehan, et al.
Plos One|January 6, 2018
The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical featureDiana Caine, Akin Nihat, Philippa Crabb, et al.
BMC Neurology|June 29, 2021
Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob diseaseAhamad Hassan, Tracy Campbell, Lee Darwent, et al.
Brain : a Journal of Neurology|April 12, 2021
Cognitive decline heralds onset of symptomatic inherited prion diseaseJoseph Mole, Simon Mead, Peter Rudge, et al.
Scientific Reports|May 18, 2022
Prion protein gene mutation detection using long-read Nanopore sequencingFrançois Kroll, Athanasios Dimitriadis, Tracy Campbell, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2022
Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort StudyDanielle Sequeira, Akin Nihat, Tzehow Mok, et al.
JAMA Neurology|March 30, 2026
High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic ExposureGargi Banerjee, Tze How Mok, Harpreet Hyare, et al.
Journal of Neurology|October 8, 2014
Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutationAndreas C Themistocleous, Robin Kennett, Masud Husain, et al.
Annals of Indian Academy of Neurology|November 19, 2019
Familial Creutzfeldt-Jakob Disease in an Indian KindredSarosh M Katrak, Apoorva Pauranik, Shrinivas B Desai, et al.
Pageof 24

Showing results (41-50 of 231) with videos related to

Sort By:
Pageof 24
Nature Reviews. Disease Primers|February 29, 2024
Creutzfeldt-Jakob disease and other prion diseasesInga Zerr, Anna Ladogana, Simon Mead, et al.
Acta Neuropathologica|May 18, 2010
Tau, prions and Aβ: the triad of neurodegenerationLilla Reiniger, Ana Lukic, Jacqueline Linehan, et al.
Plos One|January 6, 2018
The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical featureDiana Caine, Akin Nihat, Philippa Crabb, et al.
BMC Neurology|June 29, 2021
Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob diseaseAhamad Hassan, Tracy Campbell, Lee Darwent, et al.
Brain : a Journal of Neurology|April 12, 2021
Cognitive decline heralds onset of symptomatic inherited prion diseaseJoseph Mole, Simon Mead, Peter Rudge, et al.
Scientific Reports|May 18, 2022
Prion protein gene mutation detection using long-read Nanopore sequencingFrançois Kroll, Athanasios Dimitriadis, Tracy Campbell, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2022
Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort StudyDanielle Sequeira, Akin Nihat, Tzehow Mok, et al.
JAMA Neurology|March 30, 2026
High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic ExposureGargi Banerjee, Tze How Mok, Harpreet Hyare, et al.
Journal of Neurology|October 8, 2014
Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutationAndreas C Themistocleous, Robin Kennett, Masud Husain, et al.
Annals of Indian Academy of Neurology|November 19, 2019
Familial Creutzfeldt-Jakob Disease in an Indian KindredSarosh M Katrak, Apoorva Pauranik, Shrinivas B Desai, et al.
Pageof 24