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Simon Mead

Showing results (151-160 of 231) with videos related to

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Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
BMJ (Clinical Research Ed.)|October 17, 2013
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale surveyO Noel Gill, Yvonne Spencer, Angela Richard-Loendt, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.
Archives of Neurology|April 17, 2008
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin geneJonathan D Rohrer, Jason D Warren, Rohani Omar, et al.
Brain : a Journal of Neurology|February 28, 2012
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresColin J Mahoney, Jon Beck, Jonathan D Rohrer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2022
Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenonGargi Banerjee, Kiran Samra, Matthew E Adams, et al.
Brain Communications|September 21, 2020
Putaminal diffusion tensor imaging measures predict disease severity across human prion diseasesHarpreet Hyare, Enrico De Vita, Marie-Claire Porter, et al.
Journal of Alzheimer'S Disease : JAD|February 6, 2013
Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutationsRachael I Scahill, Gerard R Ridgway, Jonathan W Bartlett, et al.
The Lancet. Neurology|October 26, 2016
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case seriesNatalie S Ryan, Jennifer M Nicholas, Philip S J Weston, et al.
Pageof 24

Showing results (151-160 of 231) with videos related to

Sort By:
Pageof 24
Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
BMJ (Clinical Research Ed.)|October 17, 2013
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale surveyO Noel Gill, Yvonne Spencer, Angela Richard-Loendt, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.
Archives of Neurology|April 17, 2008
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin geneJonathan D Rohrer, Jason D Warren, Rohani Omar, et al.
Brain : a Journal of Neurology|February 28, 2012
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresColin J Mahoney, Jon Beck, Jonathan D Rohrer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2022
Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenonGargi Banerjee, Kiran Samra, Matthew E Adams, et al.
Brain Communications|September 21, 2020
Putaminal diffusion tensor imaging measures predict disease severity across human prion diseasesHarpreet Hyare, Enrico De Vita, Marie-Claire Porter, et al.
Journal of Alzheimer'S Disease : JAD|February 6, 2013
Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutationsRachael I Scahill, Gerard R Ridgway, Jonathan W Bartlett, et al.
The Lancet. Neurology|October 26, 2016
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case seriesNatalie S Ryan, Jennifer M Nicholas, Philip S J Weston, et al.
Pageof 24