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Journal of Inherited Metabolic Disease|January 1, 1989
Transient neonatal tyrosinaemiaD N Rice, I B Houston, I C Lyon, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1988
Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolismH A Simmonds, L D Fairbanks, G S Morris, 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.Clinical Science (London, England : 1979)|December 1, 1983
Importance of platelet-free preparations for evaluating lymphocyte nucleotide levels in inherited or acquired immunodeficiency syndromesA Goday, H A Simmonds, D R Webster, et al.Clinical and Experimental Immunology|October 1, 1978
Absence of oroticaciduria in adenosine deaminase deficiency and purine nucleoside phosphorylase deficiencyH A Simmonds, C F Potter, A Sahota, et al.Pediatrics|June 1, 1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS Y Pang, M A Wallace, L Hofman, et al.Journal of Inherited Metabolic Disease|January 1, 1984
Pregnancy in xanthinuria: demonstration of fetal uric acid production?H A Simmonds, J H Stutchbury, D R Webster, et al.Advances in Experimental Medicine and Biology|January 1, 1980
Spectrum of 2,8-dihydroxyadenine urolithiasis in complete APRT deficiencyH A Simmonds, T M Barratt, D R Webster, et al.Pageof 5