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Pediatric Research|January 1, 1980
Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoproteinS I Goodman, E R McCabe, P V Fennessey, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiencyS I Goodman, E R McCabe, P V Fennessey, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challengeS 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
Critical Care Medicine|September 29, 2000
A new approach to Advance DirectivesS Pollack
Israel Journal of Medical Sciences|October 1, 1993
Epidemiological and immunological study of HIV-seropositive Ethiopian immigrants in Israel. The Israel AIDS Study GroupS Pollack
Clinics in Perinatology|December 13, 1997
Catastrophic metabolic encephalopathies in the newborn period. Evaluation and managementC L Greene, S I Goodman
Proceedings 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 Goodman
The 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 Goodman
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