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Simon Mead

Showing results (51-60 of 231) with videos related to

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Brain : a Journal of Neurology|January 31, 2019
Early neurophysiological biomarkers and spinal cord pathology in inherited prion diseasePeter Rudge, Zane Jaunmuktane, Harpreet Hyare, et al.
Lancet (London, England)|June 27, 2006
Kuru in the 21st century--an acquired human prion disease with very long incubation periodsJohn Collinge, Jerome Whitfield, Edward McKintosh, et al.
BMC Neurology|December 11, 2012
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob diseaseChristopher Carswell, Andrew Thompson, Ana Lukic, et al.
The American Journal of Psychiatry|March 4, 2014
Behavioral and psychiatric symptoms in prion diseaseAndrew Thompson, Angus MacKay, Peter Rudge, et al.
Brain Communications|September 21, 2020
Enteral feeding is associated with longer survival in the advanced stages of prion diseaseKirsty McNiven, Akin Nihat, Tze How Mok, et al.
Annals of Neurology|September 14, 2006
Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromesJonathan D Rohrer, Simon Mead, Rohani Omar, et al.
Journal of Alzheimer'S Disease : JAD|April 13, 2013
The presenilin 1 P264L mutation presenting as non-fluent/agrammatic primary progressive aphasiaColin J Mahoney, Laura E Downey, Jon Beck, et al.
Human Mutation|June 14, 2008
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platformsSimon Mead, Mark Poulter, John Beck, et al.
Scientific Reports|March 5, 2021
Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseasesTze How Mok, Akin Nihat, Connie Luk, et al.
Lancet (London, England)|January 30, 2010
Variant CJD in an individual heterozygous for PRNP codon 129Diego Kaski, Simon Mead, Harpreet Hyare, et al.
Pageof 24

Showing results (51-60 of 231) with videos related to

Sort By:
Pageof 24
Brain : a Journal of Neurology|January 31, 2019
Early neurophysiological biomarkers and spinal cord pathology in inherited prion diseasePeter Rudge, Zane Jaunmuktane, Harpreet Hyare, et al.
Lancet (London, England)|June 27, 2006
Kuru in the 21st century--an acquired human prion disease with very long incubation periodsJohn Collinge, Jerome Whitfield, Edward McKintosh, et al.
BMC Neurology|December 11, 2012
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob diseaseChristopher Carswell, Andrew Thompson, Ana Lukic, et al.
The American Journal of Psychiatry|March 4, 2014
Behavioral and psychiatric symptoms in prion diseaseAndrew Thompson, Angus MacKay, Peter Rudge, et al.
Brain Communications|September 21, 2020
Enteral feeding is associated with longer survival in the advanced stages of prion diseaseKirsty McNiven, Akin Nihat, Tze How Mok, et al.
Annals of Neurology|September 14, 2006
Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromesJonathan D Rohrer, Simon Mead, Rohani Omar, et al.
Journal of Alzheimer'S Disease : JAD|April 13, 2013
The presenilin 1 P264L mutation presenting as non-fluent/agrammatic primary progressive aphasiaColin J Mahoney, Laura E Downey, Jon Beck, et al.
Human Mutation|June 14, 2008
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platformsSimon Mead, Mark Poulter, John Beck, et al.
Scientific Reports|March 5, 2021
Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseasesTze How Mok, Akin Nihat, Connie Luk, et al.
Lancet (London, England)|January 30, 2010
Variant CJD in an individual heterozygous for PRNP codon 129Diego Kaski, Simon Mead, Harpreet Hyare, et al.
Pageof 24