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Journal of Developmental and Behavioral Pediatrics : JDBP|June 1, 1983
Pediatric diagnosis and management of children with developmental disabilitiesJ A BrowderDevelopmental Medicine and Child Neurology|October 1, 1975
Adoption and foster care of handicapped children in the United StatesJ A BrowderJournal of Inherited Metabolic Disease|October 27, 2004
Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challengeS I GoodmanBiochemical Medicine|February 1, 1984
Defective imino acid metabolism in hypoglycin-treated ratsS I Goodman, D ValleJournal of Developmental and Behavioral Pediatrics : JDBP|December 1, 1986
Augmentative communication, evolution, and progress for nonspeaking childrenJ A Browder, D E Anderson, M MeekClinics in Perinatology|December 13, 1997
Catastrophic metabolic encephalopathies in the newborn period. Evaluation and managementC L Greene, S I GoodmanProceedings of the National Academy of Sciences of the United States of America|July 1, 1985
Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblastsF E Frerman, S I GoodmanThe Journal of Biological Chemistry|March 25, 1986
The purification and characterization of glutaryl-coenzyme A dehydrogenase from porcine and human liverA C Lenich, S I GoodmanJournal of Inherited Metabolic Disease|January 1, 1984
Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency)S I Goodman, F E FrermanPageof 8