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Transplantation|May 1, 1992
The importance of thiopurine methyltransferase activity for the use of azathioprine in transplant recipientsP R Chocair, J A Duley, H A Simmonds, et al.
The American Journal of Physiology|August 1, 1980
Micropuncture study of tubular transport of urate and PAH in the pig kidneyF Roch-Ramel, F White, L Vowles, et al.
Clinical Nephrology|October 1, 1980
Familial gout and renal failure in young womenH A Simmonds, D J Warren, J S Cameron, 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.
Lancet (London, England)|July 10, 1993
Low-dose allopurinol plus azathioprine/cyclosporin/prednisolone, a novel immunosuppressive regimenP Chocair, J Duley, H A Simmonds, et al.
The Quarterly Journal of Medicine|June 1, 1993
Fast and slow methylators: do racial differences influence risk of allograft rejection?P R Chocair, J A Duley, E Sabbaga, et al.
Clinical Nephrology|December 1, 1975
Experimental crystal nephropathy (one year study in the pig)D A Farebrother, P Hatfield, H A Simmonds, et al.
Clinical and Experimental Immunology|October 1, 1978
Absence of oroticaciduria in adenosine deaminase deficiency and purine nucleoside phosphorylase deficiencyH A Simmonds, C F Potter, A Sahota, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1989
Purine enzyme defects as a cause of acute renal failure in childhoodH A Simmonds, J S Cameron, T M Barratt, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1986
2,8-Dihydroxyadenine lithiasisH A Simmonds
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