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Journal of Cancer Education : the Official Journal of the American Association for Cancer Education
|
January 1, 1991
Information needs of families of cancer patients: a literature review and recommendations
P S Houts, I Rusenas, M A Simmonds, et al.
Acta Biochimica Polonica
|
January 1, 1994
Substrate specificity of methylthioadenosine phosphorylase from human liver
K Fabianowska-Majewska, J Duley, L Fairbanks, et al.
Biochemical Pharmacology
|
March 1, 1984
Metabolism of deoxynucleosides by lymphocytes in long-term culture deficient in different purine enzymes
H A Simmonds, A Goday, G S Morris, et al.
Biochemical Pharmacology
|
July 15, 1983
On the metabolism of allopurinol. Formation of allopurinol-1-riboside in purine nucleoside phosphorylase deficiency
S Reiter, H A Simmonds, D R Webster, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
An alternative pathway of adenylate and ATP synthesis
C Montero, R T Smolenski, J A Duley, et al.
Biomedical Chromatography : BMC
|
July 1, 1991
A high performance liquid chromatographic assay for AMP-deaminase activity in the erythrocytes of healthy subjects and patients with inherited purine disorders
R T Smolenski, C Montero, A V Rodgers, et al.
Clinical Science (London, England : 1979)
|
March 1, 1991
Orotidine accumulation in human erythrocytes during allopurinol therapy: association with high urinary oxypurinol-7-riboside concentrations in renal failure and in the Lesch-Nyhan syndrome
H A Simmonds, S Reiter, P M Davies, et al.
Annals of the Rheumatic Diseases
|
August 1, 1980
Tienilic acid: a single treatment for hyperuricaemia and hypertension?
T Gibson, V A Rodgers, C F Potter, et al.
The American Journal of Physiology
|
June 1, 1976
Uric acid excretion by the pig kidney
H A Simmonds, P J Hatfield, J S Cameron, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Urinary uracil concentrations are a useful guide to genetic disorders associated with neurological deficits and abnormal pyrimidine metabolism
P M Davies, L D Fairbanks, J A Duley, et al.
Page
of 41
Search research articles
Search
Showing results (191-200 of 401) with videos related to
Sort By:
Page
of 41
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education
|
January 1, 1991
Information needs of families of cancer patients: a literature review and recommendations
P S Houts, I Rusenas, M A Simmonds, et al.
Acta Biochimica Polonica
|
January 1, 1994
Substrate specificity of methylthioadenosine phosphorylase from human liver
K Fabianowska-Majewska, J Duley, L Fairbanks, et al.
Biochemical Pharmacology
|
March 1, 1984
Metabolism of deoxynucleosides by lymphocytes in long-term culture deficient in different purine enzymes
H A Simmonds, A Goday, G S Morris, et al.
Biochemical Pharmacology
|
July 15, 1983
On the metabolism of allopurinol. Formation of allopurinol-1-riboside in purine nucleoside phosphorylase deficiency
S Reiter, H A Simmonds, D R Webster, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
An alternative pathway of adenylate and ATP synthesis
C Montero, R T Smolenski, J A Duley, et al.
Biomedical Chromatography : BMC
|
July 1, 1991
A high performance liquid chromatographic assay for AMP-deaminase activity in the erythrocytes of healthy subjects and patients with inherited purine disorders
R T Smolenski, C Montero, A V Rodgers, et al.
Clinical Science (London, England : 1979)
|
March 1, 1991
Orotidine accumulation in human erythrocytes during allopurinol therapy: association with high urinary oxypurinol-7-riboside concentrations in renal failure and in the Lesch-Nyhan syndrome
H A Simmonds, S Reiter, P M Davies, et al.
Annals of the Rheumatic Diseases
|
August 1, 1980
Tienilic acid: a single treatment for hyperuricaemia and hypertension?
T Gibson, V A Rodgers, C F Potter, et al.
The American Journal of Physiology
|
June 1, 1976
Uric acid excretion by the pig kidney
H A Simmonds, P J Hatfield, J S Cameron, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Urinary uracil concentrations are a useful guide to genetic disorders associated with neurological deficits and abnormal pyrimidine metabolism
P M Davies, L D Fairbanks, J A Duley, et al.
Page
of 41