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Canadian Family Physician Medecin De Famille Canadien|January 22, 2011
Metabolic diseases in childrenD A Applegarth, J E DimmickPediatric Clinics of North America|February 1, 1989
Laboratory detection of metabolic diseaseD A Applegarth, J E Dimmick, J R TooneAmerican Journal of Medical Genetics|December 1, 1988
Juvenile galactosialidosis in a white male: a new variantD Chitayat, D A Applegarth, J Lewis, et al.Prenatal Diagnosis|January 1, 1985
Prenatal diagnosis of pyruvate carboxylase deficiencyB H Robinson, J R Toone, R P Benedict, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1990
The high incidence of valproate hepatotoxicity in infants may relate to familial metabolic defectsR E Appleton, K Farrell, D A Applegarth, et al.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.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 1975
Interpretation of elevated blood glycine levels in childrenD A Applegarth, S PoonDigestive Diseases and Sciences|April 1, 1991
Unique features of Helicobacter pylori disease in childrenE Hassall, J E DimmickPediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 27, 1999
Histopathologic approach to metabolic liver disease: Part 2G P Jevon, J E DimmickMolecular Genetics and Metabolism|October 11, 2001
Nonketotic hyperglycinemia (glycine encephalopathy): laboratory diagnosisD A Applegarth, J R ToonePageof 11