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Clinica Chimica Acta; International Journal of Clinical Chemistry|January 17, 1977
Cystic fibrosis: the effect of medium from cultured cystic fibrosis fibroblasts on ATPase activityD A Applegarth, A G Davidson, E M Haworth, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 1975
Interpretation of elevated blood glycine levels in childrenD A Applegarth, S PoonCanadian Family Physician Medecin De Famille Canadien|January 22, 2011
Metabolic diseases in childrenD A Applegarth, J E DimmickMolecular Genetics and Metabolism|October 11, 2001
Nonketotic hyperglycinemia (glycine encephalopathy): laboratory diagnosisD A Applegarth, J R TooneJournal of Inherited Metabolic Disease|January 1, 1980
Uptake of lysosomal enzymes by human fibroblasts: lack of uptake of fungal or plant glycosidases in comparison with a mammalian enzymeK C Dooley, D A ApplegarthClinical Biochemistry|April 1, 1979
Hyperprolinemia type II: evidence of the excretion of 3-hydroxy delta 1-pyrroline 5-carboxylic acidK C Dooley, D A ApplegarthJournal 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 ApplegarthPageof 15