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Showing results (141-150 of 173) with videos related to

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The Lancet. Neurology|April 25, 2006
Predicting susceptibility and incubation time of human-to-human transmission of vCJDM T Bishop, P Hart, L Aitchison, et al.
Neurology|December 15, 2004
A case-control study of sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of clusteringL Linsell, S N Cousens, P G Smith, et al.
European Journal of Neurology|August 8, 2008
MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter-observer agreement studyA Krasnianski, K Kallenberg, D A Collie, et al.
Nature|October 23, 1997
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agentM E Bruce, R G Will, J W Ironside, et al.
Lancet (London, England)|May 3, 2000
The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob diseaseM Zeidler, R J Sellar, D A Collie, et al.
Annals of Neurology|June 3, 2004
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002Mark W Head, Tristan J R Bunn, Matthew T Bishop, et al.
BMC Infectious Diseases|January 13, 2006
Comparative evidence for a link between Peyer's patch development and susceptibility to transmissible spongiform encephalopathiesSuzanne G St Rose, Nora Hunter, Louise Matthews, et al.
Lancet (London, England)|October 7, 1997
New variant Creutzfeldt-Jakob disease: neurological features and diagnostic testsM Zeidler, G E Stewart, C R Barraclough, et al.
Annals of Neurology|April 1, 2009
Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strainJean-Philippe Brandel, Craig A Heath, Mark W Head, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 22, 2006
Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UKC A Heath, R A Barker, T F G Esmonde, et al.
Pageof 18

Showing results (141-150 of 173) with videos related to

Sort By:
Pageof 18
The Lancet. Neurology|April 25, 2006
Predicting susceptibility and incubation time of human-to-human transmission of vCJDM T Bishop, P Hart, L Aitchison, et al.
Neurology|December 15, 2004
A case-control study of sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of clusteringL Linsell, S N Cousens, P G Smith, et al.
European Journal of Neurology|August 8, 2008
MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter-observer agreement studyA Krasnianski, K Kallenberg, D A Collie, et al.
Nature|October 23, 1997
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agentM E Bruce, R G Will, J W Ironside, et al.
Lancet (London, England)|May 3, 2000
The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob diseaseM Zeidler, R J Sellar, D A Collie, et al.
Annals of Neurology|June 3, 2004
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002Mark W Head, Tristan J R Bunn, Matthew T Bishop, et al.
BMC Infectious Diseases|January 13, 2006
Comparative evidence for a link between Peyer's patch development and susceptibility to transmissible spongiform encephalopathiesSuzanne G St Rose, Nora Hunter, Louise Matthews, et al.
Lancet (London, England)|October 7, 1997
New variant Creutzfeldt-Jakob disease: neurological features and diagnostic testsM Zeidler, G E Stewart, C R Barraclough, et al.
Annals of Neurology|April 1, 2009
Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strainJean-Philippe Brandel, Craig A Heath, Mark W Head, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 22, 2006
Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UKC A Heath, R A Barker, T F G Esmonde, et al.
Pageof 18