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The Journal of Pediatrics|March 1, 1992
Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiencyA Davidson-Mundt, A S Luder, C L GreeneAmerican Journal of Obstetrics and Gynecology|November 1, 1989
Maternal phenylketonuria and hyperphenylalaninemia: implications for medical practice in the United StatesA S Luder, C L GreeneClinics in Perinatology|December 13, 1997
Catastrophic metabolic encephalopathies in the newborn period. Evaluation and managementC L Greene, S I GoodmanThe Journal of Pediatrics|October 1, 1993
Molybdenum cofactor deficiencyG L Arnold, C L Greene, J P Stout, et al.International Journal of Cardiology|September 1, 1987
Very early presentation of Pompe's disease and its cross-sectional echocardiographic featuresA Lorber, A S LuderPediatric Pulmonology|October 17, 1998
Hypoxia and chest pain due to acute constipation: an underdiagnosed condition?A S Luder, D Segal, N SabaMilitary Medicine|September 30, 2000
Physiological and practical evaluation of a biological/chemical protective device for infantsI Amirav, Y Epstien, A S LuderJournal of Inherited Metabolic Disease|October 27, 2004
Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challengeS I GoodmanJournal of Inherited Metabolic Disease|January 1, 1992
Persistent hypermethioninaemia with dominant inheritanceH J Blom, A J Davidson, J D Finkelstein, et al.Postgraduate Medical Journal|April 1, 1980
Nephrotic syndrome complicated by tubular dysfunction. Case report and review of possible mechanismsA S Luder, S L Cohen, C FisherPageof 154