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S I Goodman

Showing results (11-20 of 130) with videos related to

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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
Biochemical Medicine|June 1, 1975
Glutaric aciduria: inherited deficiency of glutaryl-CoA dehydrogenase activityS I Goodman, J G Kohlhoff
Clinical Chemistry|March 1, 1970
A gas chromatographic procedure for detection of pathological organic aciduriaK B Hammond, S I Goodman
Seminars in Perinatology|February 1, 1991
Inborn errors as causes of acute disease in infancyS I Goodman, C L Greene
Clinical Genetics|January 1, 1974
Detection of inborn errors of metabolism. II. Defects in propionic acid metabolismH Z Hill, S I Goodman
Progress in Clinical and Biological Research|January 1, 1990
Progress in cloning the gene for electron transfer flavoprotein:ubiquinone oxidoreductaseS I Goodman, F E Frerman
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
Journal of Inherited Metabolic Disease|January 1, 1984
Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency)S I Goodman, F E Frerman
Laboratory and Research Methods in Biology and Medicine|January 1, 1981
Diagnosis of organic acidemias by gas chromatography--mass spectrometryS I Goodman, S P Markey
Lancet (London, England)|November 28, 1970
Hydroxylysinuria in association with trisomy 21S I Goodman, J A Browder
Pageof 13

Showing results (11-20 of 130) with videos related to

Sort By:
Pageof 13
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
Biochemical Medicine|June 1, 1975
Glutaric aciduria: inherited deficiency of glutaryl-CoA dehydrogenase activityS I Goodman, J G Kohlhoff
Clinical Chemistry|March 1, 1970
A gas chromatographic procedure for detection of pathological organic aciduriaK B Hammond, S I Goodman
Seminars in Perinatology|February 1, 1991
Inborn errors as causes of acute disease in infancyS I Goodman, C L Greene
Clinical Genetics|January 1, 1974
Detection of inborn errors of metabolism. II. Defects in propionic acid metabolismH Z Hill, S I Goodman
Progress in Clinical and Biological Research|January 1, 1990
Progress in cloning the gene for electron transfer flavoprotein:ubiquinone oxidoreductaseS I Goodman, F E Frerman
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
Journal of Inherited Metabolic Disease|January 1, 1984
Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency)S I Goodman, F E Frerman
Laboratory and Research Methods in Biology and Medicine|January 1, 1981
Diagnosis of organic acidemias by gas chromatography--mass spectrometryS I Goodman, S P Markey
Lancet (London, England)|November 28, 1970
Hydroxylysinuria in association with trisomy 21S I Goodman, J A Browder
Pageof 13