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S I Goodman

Showing results (41-50 of 130) with videos related to

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The New England Journal of Medicine|June 30, 1988
Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthoodR Carmel, D Watkins, S I Goodman, et al.
Journal of Chromatography|November 11, 1977
Organic acid profiles of human tissue biopsies by capillary gas chromatography-mass spectrometryS I Goodman, P Helland, O Stokke, et al.
Biochemical Medicine|April 1, 1975
Glutaric aciduria; presence of glutaconic and beta-hydroxyglutaric acids in urineO Stokke, S I Goodman, J A Thompson, et al.
Blood|April 1, 1980
Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression testR Carmel, A A Bedros, J W Mace, et al.
American Journal of Human Genetics|November 1, 1984
Carrier screening for phenylketonuria: comparison of two discriminant analysis proceduresC L Freehauf, D Lezotte, S I Goodman, et al.
Clinical Biochemistry|February 1, 1977
Hyperprolinemia type II: identification of the glycine conjugate of pyrrole-2-carboxylic acid in urineD A Applegarth, S I Goodman, D G Irvine, et al.
Human Molecular Genetics|February 1, 1995
Characterization of a mutation that abolishes quinone reduction by electron transfer flavoprotein-ubiquinone oxidoreductaseS E Beard, S I Goodman, K Bemelen, et al.
Human Molecular Genetics|April 1, 1994
TaqI polymorphism in intron 2 of the GCDH geneJ C Haworth, R Singal, S I Goodman, et al.
Pediatric Research|March 1, 1986
Stable isotope dilution analysis of isovalerylglycine in amniotic fluid and urine and its application for the prenatal diagnosis of isovaleric acidemiaD G Hine, A M Hack, S I Goodman, et al.
The Journal of Pediatrics|June 1, 1989
Transient nonketotic hyperglycinemia in neonatesA S Luder, A Davidson, S I Goodman, et al.
Pageof 13

Showing results (41-50 of 130) with videos related to

Sort By:
Pageof 13
The New England Journal of Medicine|June 30, 1988
Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthoodR Carmel, D Watkins, S I Goodman, et al.
Journal of Chromatography|November 11, 1977
Organic acid profiles of human tissue biopsies by capillary gas chromatography-mass spectrometryS I Goodman, P Helland, O Stokke, et al.
Biochemical Medicine|April 1, 1975
Glutaric aciduria; presence of glutaconic and beta-hydroxyglutaric acids in urineO Stokke, S I Goodman, J A Thompson, et al.
Blood|April 1, 1980
Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression testR Carmel, A A Bedros, J W Mace, et al.
American Journal of Human Genetics|November 1, 1984
Carrier screening for phenylketonuria: comparison of two discriminant analysis proceduresC L Freehauf, D Lezotte, S I Goodman, et al.
Clinical Biochemistry|February 1, 1977
Hyperprolinemia type II: identification of the glycine conjugate of pyrrole-2-carboxylic acid in urineD A Applegarth, S I Goodman, D G Irvine, et al.
Human Molecular Genetics|February 1, 1995
Characterization of a mutation that abolishes quinone reduction by electron transfer flavoprotein-ubiquinone oxidoreductaseS E Beard, S I Goodman, K Bemelen, et al.
Human Molecular Genetics|April 1, 1994
TaqI polymorphism in intron 2 of the GCDH geneJ C Haworth, R Singal, S I Goodman, et al.
Pediatric Research|March 1, 1986
Stable isotope dilution analysis of isovalerylglycine in amniotic fluid and urine and its application for the prenatal diagnosis of isovaleric acidemiaD G Hine, A M Hack, S I Goodman, et al.
The Journal of Pediatrics|June 1, 1989
Transient nonketotic hyperglycinemia in neonatesA S Luder, A Davidson, S I Goodman, et al.
Pageof 13