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Pediatric Research|March 1, 1986
Biochemical and histologic pathology in an infant with cross-reacting material (negative) pyruvate carboxylase deficiencyL T Wong, A G Davidson, D A Applegarth, et al.Journal of Inherited Metabolic Disease|July 27, 2004
Glycine encephalopathy (nonketotic hyperglycinaemia) : review and updateD A Applegarth, J R TooneMedical Hypotheses|June 1, 1983
Is cystic fibrosis a disease confined to epithelial cells?D A Applegarth, M A BridgesJournal of Inherited Metabolic Disease|January 1, 1989
Use of placental enzyme analysis in assessment of the newborn at risk for non-ketotic hyperglycinaemia (NKH)J R Toone, D A ApplegarthBiochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|February 24, 2001
Glycine cleavage enzyme complex: rabbit H-protein cDNA sequence analysis and comparison to human, cow, and chickenF Choy, L Sharp, D A ApplegarthClinical Biochemistry|June 1, 1975
Analysis of urinary mucopolysaccharides using small ion exchange columnsD A Applegarth, G Bozoian, R B LowryPediatric Clinics of North America|February 1, 1989
Laboratory detection of metabolic diseaseD A Applegarth, J E Dimmick, J R ToonePediatric Pathology|January 1, 1983
Laboratory diagnosis of inborn errors of metabolism in childrenD A Applegarth, J R Toone, P M MacLeodPediatrics|January 5, 2000
Incidence of inborn errors of metabolism in British Columbia, 1969-1996D A Applegarth, J R Toone, R B LowryJournal of Inherited Metabolic Disease|January 1, 1992
Prenatal diagnosis of non-ketotic hyperglycinaemiaJ R Toone, D A Applegarth, H L LevyPageof 14