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A Simmonds

Showing results (211-220 of 401) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
Heterogeneity of symptomatology in two male siblings with thymine uraciluriaM J Henderson, S Jones, P Walker, et al.
European Journal of Clinical Investigation|August 1, 1980
Purine and pyrimidine metabolism in hereditary orotic aciduria: some unexpected effects of allopurinolH A Simmonds, D R Webster, D M Becroft, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
Genetic mechanism(s) responsible for a deficiency of adenine phosphoribosyltransferase in manJ M Wilson, P E Daddona, H A Simmonds, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Pyrimidine and purine metabolites in ornithine carbamoyl transferase deficiencyD R Webster, H A Simmonds, D M Barry, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Inheritance of adenine phosphoribosyltransferase (APRT) deficiencyK J Van Acker, H A Simmonds, C F Potter, et al.
Advances in Experimental Medicine and Biology|January 1, 1977
Purine excretion in complete adenine phosphoribosyltransferase deficiency: effect of diet and allopurinol therapyH A Simmonds, K J Van Acker, J S Cameron, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiencyD M Becroft, D M Barry, D R Webster, et al.
Annals of the Rheumatic Diseases|July 1, 1973
Acute intratubular crystal deposition causing permanent renal damage in the pigP J Hatfield, H A Simmonds, D A Farebrother, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1990
Demonstration of a combined deficiency of xanthine oxidase and aldehyde oxidase in xanthinuric patients not forming oxipurinolS Reiter, H A Simmonds, N Zöllner, et al.
QJM : Monthly Journal of the Association of Physicians|January 30, 2004
Familial juvenile hyperuricaemic nephropathyL D Fairbanks, A M Marinaki, H A Simmonds, et al.
Pageof 41

Showing results (211-220 of 401) with videos related to

Sort By:
Pageof 41
Journal of Inherited Metabolic Disease|January 1, 1995
Heterogeneity of symptomatology in two male siblings with thymine uraciluriaM J Henderson, S Jones, P Walker, et al.
European Journal of Clinical Investigation|August 1, 1980
Purine and pyrimidine metabolism in hereditary orotic aciduria: some unexpected effects of allopurinolH A Simmonds, D R Webster, D M Becroft, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
Genetic mechanism(s) responsible for a deficiency of adenine phosphoribosyltransferase in manJ M Wilson, P E Daddona, H A Simmonds, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Pyrimidine and purine metabolites in ornithine carbamoyl transferase deficiencyD R Webster, H A Simmonds, D M Barry, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Inheritance of adenine phosphoribosyltransferase (APRT) deficiencyK J Van Acker, H A Simmonds, C F Potter, et al.
Advances in Experimental Medicine and Biology|January 1, 1977
Purine excretion in complete adenine phosphoribosyltransferase deficiency: effect of diet and allopurinol therapyH A Simmonds, K J Van Acker, J S Cameron, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiencyD M Becroft, D M Barry, D R Webster, et al.
Annals of the Rheumatic Diseases|July 1, 1973
Acute intratubular crystal deposition causing permanent renal damage in the pigP J Hatfield, H A Simmonds, D A Farebrother, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1990
Demonstration of a combined deficiency of xanthine oxidase and aldehyde oxidase in xanthinuric patients not forming oxipurinolS Reiter, H A Simmonds, N Zöllner, et al.
QJM : Monthly Journal of the Association of Physicians|January 30, 2004
Familial juvenile hyperuricaemic nephropathyL D Fairbanks, A M Marinaki, H A Simmonds, et al.
Pageof 41