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British Journal of Pharmacology|March 1, 1986
Prostaglandin endoperoxide analogues which are both thromboxane receptor antagonists and prostacyclin mimeticsR A Armstrong, R L Jones, J MacDermot, et al.
Boletin De La Asociacion Medica De Puerto Rico|September 12, 1998
Epidemiological trends of melanoma in Puerto Rico from 1975-1991J L Matta, C M Nazario, R A Armstrong, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt-Jakob disease (vCJD)R A Armstrong, J W Ironside, P L Lantos, et al.
Clinical Neuropathology|October 9, 2003
Differences in the density and spatial distribution of florid and diffuse plaques in variant Creutzfeldt-Jakob disease (vCJD)R A Armstrong, P L Lantos, J W Ironside, et al.
Pathophysiology : the Official Journal of the International Society for Pathophysiology|July 9, 2002
Quantitative variations in the pathology of 11 cases of variant Creutzfeldt-Jakob disease (vCJD)R A. Armstrong, N J. Cairns, J W. Ironside, et al.
Gerontology|January 1, 1993
Morphometric analysis of the muscle fibres of the soleus muscle of the ageing rat: long-term effect of hypophysectomy and food restrictionC D Shorey, A V Everitt, R A Armstrong, et al.
Community Dental Health|March 1, 1995
Healthy decision making: a new approach in health promotion using health state utilitiesR A Armstrong, M R Brickley, J P Shepherd, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 25, 2003
Spatial correlation between the vacuolation, prion protein, deposition and surviving neurons in patients with Creutzfeldt-Jakob disease (vCJD)R A Armstrong, P L Lantos, J W Ironside, et al.
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.
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