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J Collinge

Showing results (81-90 of 171) with videos related to

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The Journal of Pediatrics|June 1, 1986
Family support system in newborn medicine: does it work? Follow-up study of infants at riskC Perrault, A L Coates, J Collinge, et al.
Lancet (London, England)|March 6, 1993
Prion dementiaJ Collinge, M S Palmer, M N Rossor, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 2006
Neuroimaging findings in human prion diseaseR G Macfarlane, S J Wroe, J Collinge, et al.
BMJ (Clinical Research Ed.)|January 30, 1993
Inherited prion disease (PrP lysine 200) in Britain: two case reportsJ Collinge, M S Palmer, T Campbell, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Species-barrier-independent prion replication in apparently resistant speciesA F Hill, S Joiner, J Linehan, et al.
The Journal of Trauma|October 19, 2000
Ostomy as a risk factor for posttraumatic infection in penetrating colonic injuries: univariate and multivariate analysesC J Dente, J Tyburski, R F Wilson, et al.
Human Molecular Genetics|September 1, 1995
Familial non-specific dementia maps to chromosome 3J Brown, A Ashworth, S Gydesen, et al.
Neuropathology and Applied Neurobiology|July 29, 2008
Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseasesA M Isaacs, C Powell, T E Webb, et al.
Lancet (London, England)|January 9, 1993
Transmission of Creutzfeldt-Jakob disease by handling of dura materT Weber, H Tumani, B Holdorff, et al.
American Journal of Human Genetics|November 13, 2001
Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1S Mead, S P Mahal, J Beck, et al.
Pageof 18

Showing results (81-90 of 171) with videos related to

Sort By:
Pageof 18
The Journal of Pediatrics|June 1, 1986
Family support system in newborn medicine: does it work? Follow-up study of infants at riskC Perrault, A L Coates, J Collinge, et al.
Lancet (London, England)|March 6, 1993
Prion dementiaJ Collinge, M S Palmer, M N Rossor, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 2006
Neuroimaging findings in human prion diseaseR G Macfarlane, S J Wroe, J Collinge, et al.
BMJ (Clinical Research Ed.)|January 30, 1993
Inherited prion disease (PrP lysine 200) in Britain: two case reportsJ Collinge, M S Palmer, T Campbell, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Species-barrier-independent prion replication in apparently resistant speciesA F Hill, S Joiner, J Linehan, et al.
The Journal of Trauma|October 19, 2000
Ostomy as a risk factor for posttraumatic infection in penetrating colonic injuries: univariate and multivariate analysesC J Dente, J Tyburski, R F Wilson, et al.
Human Molecular Genetics|September 1, 1995
Familial non-specific dementia maps to chromosome 3J Brown, A Ashworth, S Gydesen, et al.
Neuropathology and Applied Neurobiology|July 29, 2008
Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseasesA M Isaacs, C Powell, T E Webb, et al.
Lancet (London, England)|January 9, 1993
Transmission of Creutzfeldt-Jakob disease by handling of dura materT Weber, H Tumani, B Holdorff, et al.
American Journal of Human Genetics|November 13, 2001
Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1S Mead, S P Mahal, J Beck, et al.
Pageof 18