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Molecular Genetics and Metabolism|January 16, 1999
Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolismC R Roe, S D Cederbaum, D S Roe, et al.The Journal of Pediatrics|October 1, 1974
Combined immunodeficiency presenting as the Letterer-Siwe syndromeS D Cederbaum, G Niwayama, E R Stiehm, et al.Molecular and Cellular Biochemistry|January 1, 1983
Regulation of expression of genes for enzymes of the mammalian urea cycle in permanent cell-culture lines of hepatic and non-hepatic originD F Haggerty, E B Spector, M Lynch, et al.The Southeast Asian Journal of Tropical Medicine and Public Health|June 13, 2001
Inherited metabolic disorders in Thailand--Siriraj experienceP Wasant, J Svasti, C Srisomsap, et al.Archives of Pathology & Laboratory Medicine|December 3, 1999
Optimization of an automated DNA purification protocol for neonatal screeningE M Heath, D P O'Brien, R Banas, et al.Journal of Inherited Metabolic Disease|January 1, 1980
Intermittent non-ketotic dicarboxylic aciduria in two siblings with hypoglycaemia: an apparent defect in beta-oxidation of fatty acidsE W Naylor, L L Mosovich, R Guthrie, et al.Clinical Chemistry|November 20, 1997
Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometryD H Chace, S L Hillman, J L Van Hove, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
DNA microarray technology for neonatal screeningS F Dobrowolski, R A Banas, E W Naylor, et al.The Journal of Biological Chemistry|March 10, 1982
Regulation of glucocorticoids of arginase and argininosuccinate synthetase in cultured rat hepatoma cellsD F Haggerty, E B Spector, M Lynch, et al.Genomics|December 1, 1996
Cloning and characterization of the human type II arginase geneJ G Vockley, C P Jenkinson, H Shukla, et al.Pageof 11