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S I Goodman

Showing results (91-100 of 130) with videos related to

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Pediatrics|September 1, 1983
Hyperosmolality in small infants due to propylene glycolA M Glasgow, R L Boeckx, M K Miller, et al.
American Journal of Medical Genetics|March 1, 1989
Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathyG N Wilson, J P de Chadarévian, P Kaplan, et al.
The New England Journal of Medicine|October 9, 1980
Diagnostic importance of an increased serum anion gapP A Gabow, W D Kaehny, P V Fennessey, et al.
Acta Neuropathologica|January 1, 1989
Striatal degeneration in glutaric acidaemia type IIC W Chow, F E Frerman, S I Goodman, et al.
European Journal of Biochemistry|January 15, 1994
Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductaseS I Goodman, K M Axtell, L A Bindoff, et al.
The Journal of Pediatrics|August 1, 1977
5-oxoprolinuria: biochemical observations and case reportS P Spielberg, L I Kramer, S I Goodman, et al.
Human Mutation|August 26, 1998
Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutationsS I Goodman, D E Stein, S Schlesinger, et al.
Archives of General Psychiatry|June 1, 1986
Serotonin and 5-hydroxyindoleacetic acid in brains of suicide victims. Comparison in chronic schizophrenic patients with suicide as cause of deathE R Korpi, J E Kleinman, S I Goodman, et al.
Human Molecular Genetics|September 1, 1995
Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coliS I Goodman, L E Kratz, K A DiGiulio, et al.
Pediatric Research|July 1, 1985
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemiaD E Hale, M L Batshaw, P M Coates, et al.
Pageof 13

Showing results (91-100 of 130) with videos related to

Sort By:
Pageof 13
Pediatrics|September 1, 1983
Hyperosmolality in small infants due to propylene glycolA M Glasgow, R L Boeckx, M K Miller, et al.
American Journal of Medical Genetics|March 1, 1989
Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathyG N Wilson, J P de Chadarévian, P Kaplan, et al.
The New England Journal of Medicine|October 9, 1980
Diagnostic importance of an increased serum anion gapP A Gabow, W D Kaehny, P V Fennessey, et al.
Acta Neuropathologica|January 1, 1989
Striatal degeneration in glutaric acidaemia type IIC W Chow, F E Frerman, S I Goodman, et al.
European Journal of Biochemistry|January 15, 1994
Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductaseS I Goodman, K M Axtell, L A Bindoff, et al.
The Journal of Pediatrics|August 1, 1977
5-oxoprolinuria: biochemical observations and case reportS P Spielberg, L I Kramer, S I Goodman, et al.
Human Mutation|August 26, 1998
Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutationsS I Goodman, D E Stein, S Schlesinger, et al.
Archives of General Psychiatry|June 1, 1986
Serotonin and 5-hydroxyindoleacetic acid in brains of suicide victims. Comparison in chronic schizophrenic patients with suicide as cause of deathE R Korpi, J E Kleinman, S I Goodman, et al.
Human Molecular Genetics|September 1, 1995
Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coliS I Goodman, L E Kratz, K A DiGiulio, et al.
Pediatric Research|July 1, 1985
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemiaD E Hale, M L Batshaw, P M Coates, et al.
Pageof 13