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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 15, 1988
Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolism
H A Simmonds, L D Fairbanks, G S Morris, et al.
BMC Infectious Diseases
|
January 14, 2016
HPV Vaccine utilization, Alberta 2008/09-2013/14 School year
Xianfang C Liu, Christopher A Bell, Kimberley A Simmonds, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications
|
October 12, 1999
Simultaneous separation by high-performance liquid chromatography of carbamoyl aspartate, carbamoyl phosphate and dihydroorotic acid
L D Fairbanks, E A Carrey, K Rückemann, et al.
Cardioscience
|
December 1, 1993
Depressed adenosine and total purine catabolite production in the postischemic rat heart
R T Smolenski, H A Simmonds, P B Garlick, et al.
Clinical Nephrology
|
October 1, 1980
Familial gout and renal failure in young women
H A Simmonds, D J Warren, J S Cameron, et al.
American Journal of Public Health
|
March 1, 1991
Using a state cancer registry to increase screening behaviors of sisters and daughters of breast cancer patients
P S Houts, S L Wojtkowiak, M A Simmonds, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Adenosine deaminase deficiency with altered biochemical parameters in two sisters with late-onset immunodeficiency
L D Fairbanks, C L Shovlin, A D Webster, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
Inosine formation from hypoxanthine by intact erythrocytes and fibroblasts of an immunodeficient child with purine nucleoside phosphorylase deficiency
L D Fairbanks, D R Webster, H A Simmonds, et al.
Lancet (London, England)
|
February 25, 1999
Diagnosis of molybdenum cofactor deficiency
H A Simmonds, G F Hoffmann, J L Pérignon, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1994
Renal urate hypoexcretion in Polynesian women is not as severe as in United Kingdom (UK) women with familial juvenile hyperuricaemic nephropathy (FJHN)
M B McBride, H A Simmonds, P J Hatfield, et al.
Page
of 41
Search research articles
Search
Showing results (271-280 of 401) with videos related to
Sort By:
Page
of 41
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 15, 1988
Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolism
H A Simmonds, L D Fairbanks, G S Morris, et al.
BMC Infectious Diseases
|
January 14, 2016
HPV Vaccine utilization, Alberta 2008/09-2013/14 School year
Xianfang C Liu, Christopher A Bell, Kimberley A Simmonds, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications
|
October 12, 1999
Simultaneous separation by high-performance liquid chromatography of carbamoyl aspartate, carbamoyl phosphate and dihydroorotic acid
L D Fairbanks, E A Carrey, K Rückemann, et al.
Cardioscience
|
December 1, 1993
Depressed adenosine and total purine catabolite production in the postischemic rat heart
R T Smolenski, H A Simmonds, P B Garlick, et al.
Clinical Nephrology
|
October 1, 1980
Familial gout and renal failure in young women
H A Simmonds, D J Warren, J S Cameron, et al.
American Journal of Public Health
|
March 1, 1991
Using a state cancer registry to increase screening behaviors of sisters and daughters of breast cancer patients
P S Houts, S L Wojtkowiak, M A Simmonds, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Adenosine deaminase deficiency with altered biochemical parameters in two sisters with late-onset immunodeficiency
L D Fairbanks, C L Shovlin, A D Webster, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
Inosine formation from hypoxanthine by intact erythrocytes and fibroblasts of an immunodeficient child with purine nucleoside phosphorylase deficiency
L D Fairbanks, D R Webster, H A Simmonds, et al.
Lancet (London, England)
|
February 25, 1999
Diagnosis of molybdenum cofactor deficiency
H A Simmonds, G F Hoffmann, J L Pérignon, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1994
Renal urate hypoexcretion in Polynesian women is not as severe as in United Kingdom (UK) women with familial juvenile hyperuricaemic nephropathy (FJHN)
M B McBride, H A Simmonds, P J Hatfield, et al.
Page
of 41