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S I Goodman

Showing results (61-70 of 130) with videos related to

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Psychiatry Research|December 1, 1987
Neurotransmitter amino acids in post-mortem brains of chronic schizophrenic patientsE R Korpi, J E Kleinman, S I Goodman, et al.
Medical Biology|January 1, 1987
Relationship between tryptophan and serotonin concentrations in postmortem human brainE R Korpi, S I Goodman, J E Kleinman, et al.
Biochemical Medicine|August 1, 1972
Hydroxylysinemia; a disorder due to a defect in the metabolism of free hydroxylysineS I Goodman, J A Browder, R A Hiles, et al.
American Journal of Human Genetics|November 1, 1996
Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the AmishB J Biery, D E Stein, D H Morton, et al.
The Journal of Pediatrics|April 1, 1989
Succinic semialdehyde dehydrogenase deficiency associated with combined 4-hydroxybutyric and dicarboxylic acidurias: potential for clinical misdiagnosis based on urinary organic acid profilingK M Gibson, S I Goodman, F E Frerman, et al.
Genomics|May 1, 1994
Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysisC R Greenberg, A M Duncan, C A Gregory, et al.
The New England Journal of Medicine|January 20, 1983
Deficient biotinidase activity in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, W D Parker, et al.
Lancet (London, England)|November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiencyC R Scott, C C Teng, S I Goodman, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983
Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, R J Allen, et al.
Pageof 13

Showing results (61-70 of 130) with videos related to

Sort By:
Pageof 13
Psychiatry Research|December 1, 1987
Neurotransmitter amino acids in post-mortem brains of chronic schizophrenic patientsE R Korpi, J E Kleinman, S I Goodman, et al.
Medical Biology|January 1, 1987
Relationship between tryptophan and serotonin concentrations in postmortem human brainE R Korpi, S I Goodman, J E Kleinman, et al.
Biochemical Medicine|August 1, 1972
Hydroxylysinemia; a disorder due to a defect in the metabolism of free hydroxylysineS I Goodman, J A Browder, R A Hiles, et al.
American Journal of Human Genetics|November 1, 1996
Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the AmishB J Biery, D E Stein, D H Morton, et al.
The Journal of Pediatrics|April 1, 1989
Succinic semialdehyde dehydrogenase deficiency associated with combined 4-hydroxybutyric and dicarboxylic acidurias: potential for clinical misdiagnosis based on urinary organic acid profilingK M Gibson, S I Goodman, F E Frerman, et al.
Genomics|May 1, 1994
Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysisC R Greenberg, A M Duncan, C A Gregory, et al.
The New England Journal of Medicine|January 20, 1983
Deficient biotinidase activity in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, W D Parker, et al.
Lancet (London, England)|November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiencyC R Scott, C C Teng, S I Goodman, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983
Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, R J Allen, et al.
Pageof 13