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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.
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.
Rheumatology (Oxford, England)|October 27, 1999
Effect of methotrexate on blood purine and pyrimidine levels in patients with rheumatoid arthritisZ Smoleńska, Z Kaznowska, D Zarówny, et al.
Journal of Inherited Metabolic Disease|June 1, 1997
When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indicationsH A Simmonds, J A Duley, L D Fairbanks, et al.
The American Journal of Medicine|September 1, 1988
Treatment of proteinuric idiopathic glomerulonephritides in adults: a retrospective surveyF P Schena, J S Cameron
Kidney International|November 26, 1999
The early introduction of percutaneous renal biopsy in ItalyG B Fogazzi, J S Cameron
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