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Lancet (London, England)|July 10, 1982
An X-linked syndrome characterised by hyperuricaemia, deafness, and neurodevelopmental abnormalitiesH A Simmonds, D R Webster, J Wilson, et al.
Postgraduate Medical Journal|January 1, 1979
Hypertension, renal function and goutT Gibson, J Highton, H A Simmonds, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 30, 1990
Erythrocyte nucleotide stability and plasma hypoxanthine concentrations: improved ATP stability with short-term storage at room temperatureH A Simmonds, V Micheli, P M Davies, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
How should we treat tophaceous gout in patients with allopurinol hypersensitivity?R Grahame, H A Simmonds, M B McBride, et al.
Developmental Medicine and Child Neurology|February 12, 1998
Molybdenum cofactor deficiency-phenotypic variability in a family with a late-onset variantE F Hughes, L Fairbanks, H A Simmonds, et al.
Biomedica Biochimica Acta|January 1, 1990
Importance of the human erythrocyte in the diagnosis of inherited purine and pyrimidine disordersH A Simmonds, L D Fairbanks, J A Duley, et al.
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