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J Collinge

Showing results (61-70 of 171) with videos related to

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Lancet (London, England)|July 6, 1996
Prion protein gene analysis in new variant cases of Creutzfeldt-Jakob diseaseJ Collinge, J Beck, T Campbell, et al.
Current Opinion in Genetics & Development|June 23, 1999
Molecular biology of prion propagationJ D Wadsworth, G S Jackson, A F Hill, et al.
Folia Neuropathologica|October 27, 2001
Report on the first polish case of the Gerstmann-Sträussler-Scheinker syndromeJ Kulczycki, J Collinge, W Lojkowska, et al.
Neurology|March 1, 1997
Peripheral neuropathy in Creutzfeldt-Jakob diseaseM M Esiri, W I Gordon, J Collinge, et al.
BMJ (Clinical Research Ed.)|August 14, 1998
Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum. Tonsil biopsy helps diagnose new variant Creutzfeldt-Jakob diseaseJ Collinge, M N Rossor, D Thomas, et al.
Royal Society Open Science|March 11, 2017
Cultural factors that affected the spatial and temporal epidemiology of kuruJ T Whitfield, W H Pako, J Collinge, et al.
Neuroscience Letters|August 11, 2000
Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob diseaseS Mead, J Beck, A Dickinson, et al.
Nature|July 25, 1991
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob diseaseM S Palmer, A J Dryden, J T Hughes, et al.
Neuroscience Letters|June 20, 1994
Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locusH Houlden, R Crook, J Hardy, et al.
Neuropathology and Applied Neurobiology|March 29, 2003
Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein geneA King, L Doey, M Rossor, et al.
Pageof 18

Showing results (61-70 of 171) with videos related to

Sort By:
Pageof 18
Lancet (London, England)|July 6, 1996
Prion protein gene analysis in new variant cases of Creutzfeldt-Jakob diseaseJ Collinge, J Beck, T Campbell, et al.
Current Opinion in Genetics & Development|June 23, 1999
Molecular biology of prion propagationJ D Wadsworth, G S Jackson, A F Hill, et al.
Folia Neuropathologica|October 27, 2001
Report on the first polish case of the Gerstmann-Sträussler-Scheinker syndromeJ Kulczycki, J Collinge, W Lojkowska, et al.
Neurology|March 1, 1997
Peripheral neuropathy in Creutzfeldt-Jakob diseaseM M Esiri, W I Gordon, J Collinge, et al.
BMJ (Clinical Research Ed.)|August 14, 1998
Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum. Tonsil biopsy helps diagnose new variant Creutzfeldt-Jakob diseaseJ Collinge, M N Rossor, D Thomas, et al.
Royal Society Open Science|March 11, 2017
Cultural factors that affected the spatial and temporal epidemiology of kuruJ T Whitfield, W H Pako, J Collinge, et al.
Neuroscience Letters|August 11, 2000
Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob diseaseS Mead, J Beck, A Dickinson, et al.
Nature|July 25, 1991
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob diseaseM S Palmer, A J Dryden, J T Hughes, et al.
Neuroscience Letters|June 20, 1994
Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locusH Houlden, R Crook, J Hardy, et al.
Neuropathology and Applied Neurobiology|March 29, 2003
Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein geneA King, L Doey, M Rossor, et al.
Pageof 18