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R G Will

Showing results (111-120 of 139) with videos related to

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Lancet (London, England)|April 6, 1996
A new variant of Creutzfeldt-Jakob disease in the UKR G Will, J W Ironside, M Zeidler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein geneD Nicholl, O Windl, R de Silva, et al.
Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 2001
Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob diseaseA J Green, E J Thompson, G E Stewart, et al.
Annals of Neurology|June 18, 1998
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJDR G Will, A Alperovitch, S Poser, et al.
Annals of Neurology|May 11, 2000
Diagnosis of new variant Creutzfeldt-Jakob diseaseR G Will, M Zeidler, G E Stewart, et al.
Lancet (London, England)|April 11, 2001
Geographical distribution of variant Creutzfeldt-Jakob disease in Great Britain, 1994-2000S Cousens, P G Smith, H Ward, et al.
The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Lancet (London, England)|March 7, 2003
Deaths from variant Creutzfeldt-Jakob disease in the UKN J Andrews, C P Farrington, H J T Ward, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 22, 2010
Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UKC A Heath, S A Cooper, K Murray, et al.
Pageof 14

Showing results (111-120 of 139) with videos related to

Sort By:
Pageof 14
Lancet (London, England)|April 6, 1996
A new variant of Creutzfeldt-Jakob disease in the UKR G Will, J W Ironside, M Zeidler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein geneD Nicholl, O Windl, R de Silva, et al.
Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 2001
Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob diseaseA J Green, E J Thompson, G E Stewart, et al.
Annals of Neurology|June 18, 1998
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJDR G Will, A Alperovitch, S Poser, et al.
Annals of Neurology|May 11, 2000
Diagnosis of new variant Creutzfeldt-Jakob diseaseR G Will, M Zeidler, G E Stewart, et al.
Lancet (London, England)|April 11, 2001
Geographical distribution of variant Creutzfeldt-Jakob disease in Great Britain, 1994-2000S Cousens, P G Smith, H Ward, et al.
The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Lancet (London, England)|March 7, 2003
Deaths from variant Creutzfeldt-Jakob disease in the UKN J Andrews, C P Farrington, H J T Ward, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 22, 2010
Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UKC A Heath, S A Cooper, K Murray, et al.
Pageof 14