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Journal of Neural Transmission (Vienna, Austria : 1996)|March 24, 2005
Size frequency distribution of prion protein (PrP) aggregates in variant Creutzfeldt-Jakob disease (vCJD)R A Armstrong, N J Cairns, J W Ironside, et al.Neuropathology and Applied Neurobiology|April 26, 2002
Quantification of vacuolation ("spongiform change"), surviving neurones and prion protein deposition in eleven cases of variant Creutzfeldt-Jakob diseaseR A Armstrong, N J Cairns, J W Ironside, et al.Neuroscience Letters|August 2, 2003
Does the neuropathology of human patients with variant Creutzfeldt-Jakob disease reflect haematogenous spread of the disease?R A Armstrong, N J Cairns, J W Ironside, et al.Acta Neuropathologica|November 1, 2002
The spatial patterns of prion protein deposits in cases of variant Creutzfeldt-Jakob diseaseR A Armstrong, N J Cairns, J W Ironside, et al.Biological Psychiatry|January 1, 1995
Decreased phospholipase A2 activity in Alzheimer brainsW F Gattaz, A Maras, N J Cairns, et al.FEBS Letters|September 17, 1990
Methyllycaconitine: a selective probe for neuronal alpha-bungarotoxin binding sitesJ M Ward, V B Cockcroft, G G Lunt, et al.Neuroscience Letters|January 12, 1993
Beta A4 protein deposition in familial Alzheimer's disease with the mutation in codon 717 of the beta A4 amyloid precursor protein gene and sporadic Alzheimer's diseaseN J Cairns, A Chadwick, P L Lantos, et al.Neuroscience Letters|November 10, 1995
Neurons, intracellular and extracellular neurofibrillary tangles in subdivisions of the hippocampal cortex in normal ageing and Alzheimer's diseaseY Fukutani, K Kobayashi, I Nakamura, et al.Neuroscience|June 5, 2013
Regulation of dopamine D₃ receptor in the striatal regions and substantia nigra in diffuse Lewy body diseaseJ Sun, N J Cairns, J S Perlmutter, et al.Psychiatry and Clinical Neurosciences|August 1, 1997
Neurons and extracellular neurofibrillary tangles in the hippocampal subdivisions in early-onset familial Alzheimer's disease: a case studyY Fukutani, K Sasaki, M Mukai, et al.Pageof 19