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S I Goodman

Showing results (101-110 of 130) with videos related to

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The Journal of Pediatrics|February 5, 2000
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyG M Enns, M J Bennett, C L Hoppel, et al.
Free Radical Biology & Medicine|October 26, 2001
Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant miceT T Huang, E J Carlson, H M Kozy, et al.
Annals of Neurology|May 1, 1980
Glycerol kinase deficiency with neuromuscular, skeletal, and adrenal abnormalitiesM A Guggenheim, E R McCabe, M Roig, et al.
The Journal of Pediatrics|May 1, 1984
A juvenile form of glycerol kinase deficiency with episodic vomiting, acidemia, and stuporE I Ginns, J A Barranger, S W McClean, et al.
East African Medical Journal|August 30, 2002
Biochemical and molecular diagnosis of glutaric aciduria type 1 in a black South African male child: case reportP J Ojwang, R J Pegoraro, W M Deppe, et al.
Biochemical and Biophysical Research Communications|October 24, 1977
Human glycerol kinase deficiency with hyperglycerolemia and glyceroluriaE R McCabe, P V Fennessey, M A Guggenheim, et al.
Genomics|August 10, 1995
Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase geneD M Koeller, K A DiGiulio, S V Angeloni, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Vascular dysfunction as an additional pathomechanism in glutaric aciduria type IC Mühlhausen, S Ergün, K A Strauss, et al.
The Journal of Pediatrics|June 1, 1982
Glutaric acidemia type II: clinical, biochemical, and morphologic considerationsS I Goodman, D O Stene, E R McCabe, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Comparison of urinary acylglycines and acylcarnitines as diagnostic markers of medium-chain acyl-CoA dehydrogenase deficiencyP Rinaldo, J J O'Shea, S I Goodman, et al.
Pageof 13

Showing results (101-110 of 130) with videos related to

Sort By:
Pageof 13
The Journal of Pediatrics|February 5, 2000
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyG M Enns, M J Bennett, C L Hoppel, et al.
Free Radical Biology & Medicine|October 26, 2001
Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant miceT T Huang, E J Carlson, H M Kozy, et al.
Annals of Neurology|May 1, 1980
Glycerol kinase deficiency with neuromuscular, skeletal, and adrenal abnormalitiesM A Guggenheim, E R McCabe, M Roig, et al.
The Journal of Pediatrics|May 1, 1984
A juvenile form of glycerol kinase deficiency with episodic vomiting, acidemia, and stuporE I Ginns, J A Barranger, S W McClean, et al.
East African Medical Journal|August 30, 2002
Biochemical and molecular diagnosis of glutaric aciduria type 1 in a black South African male child: case reportP J Ojwang, R J Pegoraro, W M Deppe, et al.
Biochemical and Biophysical Research Communications|October 24, 1977
Human glycerol kinase deficiency with hyperglycerolemia and glyceroluriaE R McCabe, P V Fennessey, M A Guggenheim, et al.
Genomics|August 10, 1995
Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase geneD M Koeller, K A DiGiulio, S V Angeloni, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Vascular dysfunction as an additional pathomechanism in glutaric aciduria type IC Mühlhausen, S Ergün, K A Strauss, et al.
The Journal of Pediatrics|June 1, 1982
Glutaric acidemia type II: clinical, biochemical, and morphologic considerationsS I Goodman, D O Stene, E R McCabe, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Comparison of urinary acylglycines and acylcarnitines as diagnostic markers of medium-chain acyl-CoA dehydrogenase deficiencyP Rinaldo, J J O'Shea, S I Goodman, et al.
Pageof 13