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J Collinge

Showing results (91-100 of 171) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2005
The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion diseaseR J Cordery, K Alner, L Cipolotti, et al.
Lancet (London, England)|August 26, 1995
Transmission of fatal familial insomnia to laboratory animalsJ Collinge, M S Palmer, K C Sidle, et al.
Neurology|September 1, 1995
Frontal lobe or 'nonspecific' dementias are genetically heterogeneousA Ashworth, J Brown, S Gydesen, et al.
Neuroradiology|April 7, 2006
Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopyA D Waldman, R J Cordery, D G MacManus, et al.
Neuroscience Letters|March 31, 1995
Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's diseaseH Houlden, R Crook, K Duff, et al.
Nature Cell Biology|November 13, 1999
Strain-specific prion-protein conformation determined by metal ionsJ D Wadsworth, A F Hill, S Joiner, et al.
Brain Research. Molecular Brain Research|March 1, 1992
A dementing illness associated with a novel insertion in the prion protein geneF Owen, M Poulter, J Collinge, et al.
Lancet (London, England)|January 4, 1997
New variant Creutzfeldt-Jakob disease in FranceJ P Deslys, C I Lasmézas, N Streichenberger, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Genetic characterization of a novel familial dementiaJ Brown, S Smith, A Brun, et al.
European Journal of Neurology|June 28, 2007
A novel presenilin 1 deletion (p.L166del) associated with early onset familial Alzheimer's diseaseW D Knight, J Kennedy, S Mead, et al.
Pageof 18

Showing results (91-100 of 171) with videos related to

Sort By:
Pageof 18
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2005
The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion diseaseR J Cordery, K Alner, L Cipolotti, et al.
Lancet (London, England)|August 26, 1995
Transmission of fatal familial insomnia to laboratory animalsJ Collinge, M S Palmer, K C Sidle, et al.
Neurology|September 1, 1995
Frontal lobe or 'nonspecific' dementias are genetically heterogeneousA Ashworth, J Brown, S Gydesen, et al.
Neuroradiology|April 7, 2006
Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopyA D Waldman, R J Cordery, D G MacManus, et al.
Neuroscience Letters|March 31, 1995
Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's diseaseH Houlden, R Crook, K Duff, et al.
Nature Cell Biology|November 13, 1999
Strain-specific prion-protein conformation determined by metal ionsJ D Wadsworth, A F Hill, S Joiner, et al.
Brain Research. Molecular Brain Research|March 1, 1992
A dementing illness associated with a novel insertion in the prion protein geneF Owen, M Poulter, J Collinge, et al.
Lancet (London, England)|January 4, 1997
New variant Creutzfeldt-Jakob disease in FranceJ P Deslys, C I Lasmézas, N Streichenberger, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Genetic characterization of a novel familial dementiaJ Brown, S Smith, A Brun, et al.
European Journal of Neurology|June 28, 2007
A novel presenilin 1 deletion (p.L166del) associated with early onset familial Alzheimer's diseaseW D Knight, J Kennedy, S Mead, et al.
Pageof 18