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The Journal of Pediatrics|January 10, 2001
Laboratory evaluation of urea cycle disordersR D Steiner, S D CederbaumBiochemical Genetics|April 1, 1976
Glucose 6-phosphate dehydrogenase in rainbow troutS D Cederbaum, A YoshidaBiochimica Et Biophysica Acta|March 28, 1986
Kinetics of inhibition of rat liver and kidney arginases by proline and branched-chain amino acidsN Carvajal, S D CederbaumJournal of Inherited Metabolic Disease|January 1, 1981
Urinary pyrimidine excretion in arginase deficiencyE W Naylor, S D CederbaumClinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1977
Rapid diagnosis of pyruvate and ketoglutarate dehydrogenase deficiencies in platelet-enriched preparations from bloodJ P Blass, S D Cederbaum, R A KarkPediatric Research|December 1, 1983
Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patientsE B Spector, S C Rice, S D CederbaumClinical Chemistry|October 1, 1979
Adsorption of organic acids from amniotic fluid and urine onto silica gel before analysis by gas chromatography and combined gas chromatography/mass spectrometryV P Williams, D K Ching, S D CederbaumPageof 10