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Simon Mead

Showing results (141-150 of 231) with videos related to

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Alzheimer'S Research & Therapy|September 26, 2012
Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansionsColin J Mahoney, Laura E Downey, Gerard R Ridgway, et al.
Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.
Neurobiology of Aging|June 5, 2018
Evaluating the causality of novel sequence variants in the prion protein gene by exampleTze How Mok, Carolin Koriath, Zane Jaunmuktane, et al.
The Lancet. Neurology|December 17, 2008
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association studySimon Mead, Mark Poulter, James Uphill, et al.
Neurology|December 24, 2013
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopiesDavina J Hensman Moss, Mark Poulter, Jon Beck, et al.
Emerging Infectious Diseases|April 22, 2015
Recent US Case of Variant Creutzfeldt-Jakob Disease-Global ImplicationsAtul Maheshwari, Michael Fischer, Pierluigi Gambetti, et al.
Neurobiology of Aging|March 2, 2021
A novel presenilin 1 duplication mutation (Ile168dup) causing Alzheimer's disease associated with myoclonus, seizures and pyramidal featuresAntoinette O'Connor, Emily Abel, M R Fraser, et al.
Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2018
Plasma tau is increased in frontotemporal dementiaMartha S Foiani, Ione Oc Woollacott, Carolin Heller, et al.
Viruses|September 28, 2021
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat InsertionNicholas Brennecke, Ignazio Cali, Tze How Mok, et al.
Pageof 24

Showing results (141-150 of 231) with videos related to

Sort By:
Pageof 24
Alzheimer'S Research & Therapy|September 26, 2012
Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansionsColin J Mahoney, Laura E Downey, Gerard R Ridgway, et al.
Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.
Neurobiology of Aging|June 5, 2018
Evaluating the causality of novel sequence variants in the prion protein gene by exampleTze How Mok, Carolin Koriath, Zane Jaunmuktane, et al.
The Lancet. Neurology|December 17, 2008
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association studySimon Mead, Mark Poulter, James Uphill, et al.
Neurology|December 24, 2013
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopiesDavina J Hensman Moss, Mark Poulter, Jon Beck, et al.
Emerging Infectious Diseases|April 22, 2015
Recent US Case of Variant Creutzfeldt-Jakob Disease-Global ImplicationsAtul Maheshwari, Michael Fischer, Pierluigi Gambetti, et al.
Neurobiology of Aging|March 2, 2021
A novel presenilin 1 duplication mutation (Ile168dup) causing Alzheimer's disease associated with myoclonus, seizures and pyramidal featuresAntoinette O'Connor, Emily Abel, M R Fraser, et al.
Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2018
Plasma tau is increased in frontotemporal dementiaMartha S Foiani, Ione Oc Woollacott, Carolin Heller, et al.
Viruses|September 28, 2021
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat InsertionNicholas Brennecke, Ignazio Cali, Tze How Mok, et al.
Pageof 24