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Biochemical Medicine|February 1, 1985
Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblastsF E Frerman, S I GoodmanClinica Chimica Acta; International Journal of Clinical Chemistry|February 2, 1976
Inhibition of brain glutamate decarboxylase by glutarate, glutaconate, and beta-hydroxyglutarate: explanation of the symptoms in glutaric aciduria?O Stokke, S I Goodman, P G MoeEnzyme|January 1, 1987
Recent progress in understanding glutaric acidemiasS I Goodman, F E Frerman, J P LoehrPediatric Research|March 1, 1990
Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypesJ P Loehr, S I Goodman, F E FrermanThe Journal of Pediatrics|November 4, 2000
Age at symptom onset predicts severity of motor impairment and clinical outcome of glutaric acidemia type 1K B Bjugstad, S I Goodman, C R FreedBiochemistry|November 14, 2001
Binding, hydration, and decarboxylation of the reaction intermediate glutaconyl-coenzyme A by human glutaryl-CoA dehydrogenaseJ B Westover, S I Goodman, F E FrermanScience (New York, N.Y.)|September 20, 1974
Type 2 hyperprolinemia: absence of delta1-pyrroline-5-carboxylic acid dehydrogenase activityD L Valle, J M Phang, S I GoodmanMolecular Genetics and Metabolism|August 13, 1999
Assignment of electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence in situ hybridization and somatic cell hybridizationE B Spector, W K Seltzer, S I GoodmanJournal of Inherited Metabolic Disease|January 1, 1989
Medium-chain acyl-CoA dehydrogenase deficiency: metabolic effects and therapeutic efficacy of long-term L-carnitine supplementationW R Treem, C A Stanley, S I GoodmanJournal of Chromatography|November 11, 1977
Organic acid profiles of human tissue biopsies by capillary gas chromatography-mass spectrometryS I Goodman, P Helland, O Stokke, et al.Pageof 8