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J Collinge

Showing results (151-160 of 171) with videos related to

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Neuroscience Letters|November 23, 1992
Prion protein immunocytochemistry helps to establish the true incidence of prion diseasesP L Lantos, I S McGill, I Janota, et al.
AJNR. American Journal of Neuroradiology|March 30, 2013
Multiparameter MR imaging in the 6-OPRI variant of inherited prion diseaseE De Vita, G R Ridgway, R I Scahill, et al.
Neurology|October 21, 2011
PRION-1 scales analysis supports use of functional outcome measures in prion diseaseS Mead, M Ranopa, G S Gopalakrishnan, et al.
Neuropathology and Applied Neurobiology|February 12, 2009
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L)T Webb, S Mead, J Beck, et al.
Human Genetics|September 1, 1996
Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP geneO Windl, M Dempster, J P Estibeiro, et al.
The American Journal of Pathology|June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Brain : a Journal of Neurology|April 25, 2000
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological studyJ C Janssen, M Hall, N C Fox, et al.
Brain : a Journal of Neurology|March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factorN C Fox, A M Kennedy, R J Harvey, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2011
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutationK Alner, H Hyare, S Mead, et al.
Archives of Neurology|June 19, 2001
Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutationJ C Janssen, P L Lantos, N C Fox, et al.
Pageof 18

Showing results (151-160 of 171) with videos related to

Sort By:
Pageof 18
Neuroscience Letters|November 23, 1992
Prion protein immunocytochemistry helps to establish the true incidence of prion diseasesP L Lantos, I S McGill, I Janota, et al.
AJNR. American Journal of Neuroradiology|March 30, 2013
Multiparameter MR imaging in the 6-OPRI variant of inherited prion diseaseE De Vita, G R Ridgway, R I Scahill, et al.
Neurology|October 21, 2011
PRION-1 scales analysis supports use of functional outcome measures in prion diseaseS Mead, M Ranopa, G S Gopalakrishnan, et al.
Neuropathology and Applied Neurobiology|February 12, 2009
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L)T Webb, S Mead, J Beck, et al.
Human Genetics|September 1, 1996
Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP geneO Windl, M Dempster, J P Estibeiro, et al.
The American Journal of Pathology|June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Brain : a Journal of Neurology|April 25, 2000
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological studyJ C Janssen, M Hall, N C Fox, et al.
Brain : a Journal of Neurology|March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factorN C Fox, A M Kennedy, R J Harvey, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2011
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutationK Alner, H Hyare, S Mead, et al.
Archives of Neurology|June 19, 2001
Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutationJ C Janssen, P L Lantos, N C Fox, et al.
Pageof 18