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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1987
Abnormal podocyte CR-1 expression in glomerular diseases: association with glomerular cell proliferation and monocyte infiltrationF E Nolasco, J S Cameron, B Hartley, et al.
Clinical and Experimental Immunology|September 1, 1976
Disease activity in the nephritis of systemic lupus erythematosus in relation to serum complement concentrations. DNA-binding capacity and precipitating anti-DNA antibodyJ S Cameron, M H Lessof, C S Ogg, et al.
British Medical Journal|March 25, 1978
Relapsing polychondritis with crescentic glomerulonephritisG H Neild, J S Cameron, M H Lessof, et al.
Journal of Cardiovascular Electrophysiology|November 1, 2013
Atrioesophageal fistula during cryoballoon ablation for atrial fibrillationHae W Lim, Gregory A Cogert, Craig S Cameron, et al.
International Journal of Molecular Sciences|March 11, 2023
Participants in the Trans-Antarctic Winter Traverse Expedition Showed Increased Bacterial Load and Diversity in Saliva but Maintained Individual Differences within Stool Microbiota and Across Metabolite FingerprintsSimon J S Cameron, Arwyn Edwards, Robert J Lambert, et al.
Kidney International|June 1, 1986
Adult-onset minimal change nephrotic syndrome: a long-term follow-upF Nolasco, J S Cameron, E F Heywood, et al.
BMJ (Clinical Research Ed.)|November 14, 1992
Effect of using protocols on medical care: randomised trial of three methods of taking an antenatal historyR J Lilford, M Kelly, A Baines, et al.
Biochimica Et Biophysica Acta|July 18, 2016
Metabolomic-based biomarker discovery for non-invasive lung cancer screening: A case studyKeiron O'Shea, Simon J S Cameron, Keir E Lewis, et al.
Transplantation|December 1, 1992
In situ expression of tumor necrosis factor-alpha, interferon-gamma, and interleukin-2 receptors in renal allograft biopsiesI L Noronha, M Eberlein-Gonska, B Hartley, et al.
Nucleosides, Nucleotides & Nucleic Acids|October 27, 2006
Familial juvenile hyperuricaemic nephropathy is not such a rare genetic metabolic purine disease in BritainH A Simmonds, J S Cameron, D J Goldsmith, et al.
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