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S I Goodman

Showing results (51-60 of 130) with videos related to

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The Journal of Clinical Investigation|November 1, 1979
Genetic evidence for a common enzyme catalyzing the second step in the degradation of proline and hydroxyprolineD Valle, S I Goodman, S C Harris, et al.
Clinical Genetics|January 1, 1973
Antenatal diagnosis of argininosuccinic aciduriaS I Goodman, J W Mace, B Turner, et al.
Journal of Inherited Metabolic Disease|September 1, 2006
Infant mice with glutaric acidaemia type I have increased vulnerability to 3-nitropropionic acid toxicityK B Bjugstad, L S Crnic, S I Goodman, et al.
The Journal of Pediatrics|October 1, 1993
Molybdenum cofactor deficiencyG L Arnold, C L Greene, J P Stout, et al.
Clinical Pediatrics|January 1, 1976
The child with an unusual odor. A clinical resuméJ W Mace, S I Goodman, W R Centerwall, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 16, 1976
4-hydroxycyclohexane-1-carboxylic acid: an unusual compound isolated from the urine of children with suspected disorders of metabolismT H Bindel, P V Fennessey, B S Miles, et al.
Biochemistry|September 14, 2000
Proton abstraction reaction, steady-state kinetics, and oxidation-reduction potential of human glutaryl-CoA dehydrogenaseT M Dwyer, K S Rao, S I Goodman, et al.
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.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1982
NAD glycohydrolase: enzyme characterization using intact mammalian erythrocytesS I Goodman, R J Wyatt, J B Trepel, et al.
The Journal of Pediatrics|January 1, 1988
A case of glutaric acidemia type I: effect of riboflavin and carnitineP H Lipkin, C R Roe, S I Goodman, et al.
Pageof 13

Showing results (51-60 of 130) with videos related to

Sort By:
Pageof 13
The Journal of Clinical Investigation|November 1, 1979
Genetic evidence for a common enzyme catalyzing the second step in the degradation of proline and hydroxyprolineD Valle, S I Goodman, S C Harris, et al.
Clinical Genetics|January 1, 1973
Antenatal diagnosis of argininosuccinic aciduriaS I Goodman, J W Mace, B Turner, et al.
Journal of Inherited Metabolic Disease|September 1, 2006
Infant mice with glutaric acidaemia type I have increased vulnerability to 3-nitropropionic acid toxicityK B Bjugstad, L S Crnic, S I Goodman, et al.
The Journal of Pediatrics|October 1, 1993
Molybdenum cofactor deficiencyG L Arnold, C L Greene, J P Stout, et al.
Clinical Pediatrics|January 1, 1976
The child with an unusual odor. A clinical resuméJ W Mace, S I Goodman, W R Centerwall, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 16, 1976
4-hydroxycyclohexane-1-carboxylic acid: an unusual compound isolated from the urine of children with suspected disorders of metabolismT H Bindel, P V Fennessey, B S Miles, et al.
Biochemistry|September 14, 2000
Proton abstraction reaction, steady-state kinetics, and oxidation-reduction potential of human glutaryl-CoA dehydrogenaseT M Dwyer, K S Rao, S I Goodman, et al.
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.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1982
NAD glycohydrolase: enzyme characterization using intact mammalian erythrocytesS I Goodman, R J Wyatt, J B Trepel, et al.
The Journal of Pediatrics|January 1, 1988
A case of glutaric acidemia type I: effect of riboflavin and carnitineP H Lipkin, C R Roe, S I Goodman, et al.
Pageof 13