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Psychiatry Research
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December 1, 1987
Neurotransmitter amino acids in post-mortem brains of chronic schizophrenic patients
E R Korpi, J E Kleinman, S I Goodman, et al.
Medical Biology
|
January 1, 1987
Relationship between tryptophan and serotonin concentrations in postmortem human brain
E 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 hydroxylysine
S 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 Amish
B 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 profiling
K 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 analysis
C 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 deficiency
B Wolf, R E Grier, W D Parker, et al.
Lancet (London, England)
|
November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiency
C 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 disorder
M 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 deficiency
B Wolf, R E Grier, R J Allen, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 130) with videos related to
Sort By:
Page
of 13
Psychiatry Research
|
December 1, 1987
Neurotransmitter amino acids in post-mortem brains of chronic schizophrenic patients
E R Korpi, J E Kleinman, S I Goodman, et al.
Medical Biology
|
January 1, 1987
Relationship between tryptophan and serotonin concentrations in postmortem human brain
E 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 hydroxylysine
S 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 Amish
B 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 profiling
K 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 analysis
C 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 deficiency
B Wolf, R E Grier, W D Parker, et al.
Lancet (London, England)
|
November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiency
C 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 disorder
M 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 deficiency
B Wolf, R E Grier, R J Allen, et al.
Page
of 13