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S I Goodman

Showing results (1-10 of 130) with videos related to

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American Journal of Human Genetics|November 1, 1980
An introduction to gas chromatography-mass spectrometry and the inherited organic acidemiasS I Goodman
Advances in Pediatrics|January 1, 1986
Inherited metabolic disease in the newborn: approach to diagnosis and treatmentS I Goodman
Journal of Inherited Metabolic Disease|October 27, 2004
Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challengeS I Goodman
Prenatal Diagnosis|January 12, 2002
Prenatal diagnosis of glutaric acidemiasS I Goodman
Pediatrics|September 1, 1981
Antenatal diagnosis of defects of ureagenesisS I Goodman
The American Journal of Clinical Nutrition|November 1, 1981
Organic aciduria in the riboflavin-deficient ratS I Goodman
Pediatrics|October 1, 1970
The critically ill child: acute metabolic disease in infancy and early childhoodD O'Brien, S I Goodman
Biochemical Medicine|February 1, 1984
Defective imino acid metabolism in hypoglycin-treated ratsS I Goodman, D Valle
Blood|February 1, 1982
Abnormal deoxyuridine suppression test in congenital methylmalonic aciduria-homocystinuria without megaloblastic anemia: divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in manR Carmel, S I Goodman
Clinics in Perinatology|December 13, 1997
Catastrophic metabolic encephalopathies in the newborn period. Evaluation and managementC L Greene, S I Goodman
Pageof 13

Showing results (1-10 of 130) with videos related to

Sort By:
Pageof 13
American Journal of Human Genetics|November 1, 1980
An introduction to gas chromatography-mass spectrometry and the inherited organic acidemiasS I Goodman
Advances in Pediatrics|January 1, 1986
Inherited metabolic disease in the newborn: approach to diagnosis and treatmentS I Goodman
Journal of Inherited Metabolic Disease|October 27, 2004
Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challengeS I Goodman
Prenatal Diagnosis|January 12, 2002
Prenatal diagnosis of glutaric acidemiasS I Goodman
Pediatrics|September 1, 1981
Antenatal diagnosis of defects of ureagenesisS I Goodman
The American Journal of Clinical Nutrition|November 1, 1981
Organic aciduria in the riboflavin-deficient ratS I Goodman
Pediatrics|October 1, 1970
The critically ill child: acute metabolic disease in infancy and early childhoodD O'Brien, S I Goodman
Biochemical Medicine|February 1, 1984
Defective imino acid metabolism in hypoglycin-treated ratsS I Goodman, D Valle
Blood|February 1, 1982
Abnormal deoxyuridine suppression test in congenital methylmalonic aciduria-homocystinuria without megaloblastic anemia: divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in manR Carmel, S I Goodman
Clinics in Perinatology|December 13, 1997
Catastrophic metabolic encephalopathies in the newborn period. Evaluation and managementC L Greene, S I Goodman
Pageof 13