J S Cameron|H A Simmonds - JoVE Visualize

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British Journal of Rheumatology|October 1, 1994

Polynesian women are also at risk for hyperuricaemia and gout because of a genetic defect in renal urate handlingH A Simmonds, M B McBride, P J Hatfield, et al.

Annals of the Rheumatic Diseases|April 1, 1983

A controlled study of diet in patients with goutT Gibson, A V Rodgers, H A Simmonds, et al.

Clinical and Experimental Immunology|May 1, 1984

Prenatal diagnosis of three cases of severe combined immunodeficiency: severe T cell deficiency during the first half of gestation in fetuses with adenosine deaminase deficiencyD C Linch, R J Levinsky, C H Rodeck, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1983

Methylthioadenosine phosphorylase activity in human erythrocytesA Sahota, D R Webster, C F Potter, et al.

Nucleosides, Nucleotides & Nucleic Acids|December 2, 2004

GTP concentrations are elevated in erythrocytes of renal transplant recipients when conventional immunosuppression is replaced by the inosine monophosphate dehydrogenase inhibitor mycophenolic acid mofetil (MMF)D J A Goldsmith, E A Carrey, S M Edbury, et al.

The Clinical Investigator|July 1, 1994

Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasisS Bye, R Mallmann, J Duley, et al.

The Journal of Biological Chemistry|February 10, 1982

Human adenine phosphoribosyltransferase. Immunochemical quantitation and protein blot analysis of mutant forms of the enzymeJ M Wilson, P E Daddona, H A Simmonds, et al.

Ciba Foundation Symposium|January 1, 1978

Purine metabolism in adenosine deaminase deficiencyH A Simmonds, A Sahota, C F Potter, et al.

Clinical Nephrology|February 1, 1981

High dose frusemide in acute renal failure: a controlled trialC B Brown, C S Ogg, J S Cameron

QJM : Monthly Journal of the Association of Physicians|December 1, 1995

Early prediction of treatment outcome in idiopathic membranous nephropathyC A O'Callaghan, J S Cameron, S H Sacks

Pageof 39

Showing results (161-170 of 383) with videos related to

Sort By:

Pageof 39

British Journal of Rheumatology|October 1, 1994

Polynesian women are also at risk for hyperuricaemia and gout because of a genetic defect in renal urate handlingH A Simmonds, M B McBride, P J Hatfield, et al.

Annals of the Rheumatic Diseases|April 1, 1983

A controlled study of diet in patients with goutT Gibson, A V Rodgers, H A Simmonds, et al.

Clinical and Experimental Immunology|May 1, 1984

Prenatal diagnosis of three cases of severe combined immunodeficiency: severe T cell deficiency during the first half of gestation in fetuses with adenosine deaminase deficiencyD C Linch, R J Levinsky, C H Rodeck, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1983

Methylthioadenosine phosphorylase activity in human erythrocytesA Sahota, D R Webster, C F Potter, et al.

Nucleosides, Nucleotides & Nucleic Acids|December 2, 2004

GTP concentrations are elevated in erythrocytes of renal transplant recipients when conventional immunosuppression is replaced by the inosine monophosphate dehydrogenase inhibitor mycophenolic acid mofetil (MMF)D J A Goldsmith, E A Carrey, S M Edbury, et al.

The Clinical Investigator|July 1, 1994

Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasisS Bye, R Mallmann, J Duley, et al.

The Journal of Biological Chemistry|February 10, 1982

Human adenine phosphoribosyltransferase. Immunochemical quantitation and protein blot analysis of mutant forms of the enzymeJ M Wilson, P E Daddona, H A Simmonds, et al.

Ciba Foundation Symposium|January 1, 1978

Purine metabolism in adenosine deaminase deficiencyH A Simmonds, A Sahota, C F Potter, et al.

Clinical Nephrology|February 1, 1981

High dose frusemide in acute renal failure: a controlled trialC B Brown, C S Ogg, J S Cameron

QJM : Monthly Journal of the Association of Physicians|December 1, 1995

Early prediction of treatment outcome in idiopathic membranous nephropathyC A O'Callaghan, J S Cameron, S H Sacks

Pageof 39