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S I Goodman

Showing results (81-90 of 130) with videos related to

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The Journal of Pediatrics|January 1, 1984
Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acidR Matalon, D A Stumpf, K Michals, et al.
Biochemical Medicine|October 1, 1982
Glutaric, 3-hydroxypropionic, and lactic aciduria with metabolic acidemia, following extensive small bowel resectionE R McCabe, S I Goodman, P V Fennessey, et al.
Biochemical and Biophysical Research Communications|December 20, 1976
Normal amino acid uptake by cultured human fibroblasts does not require gamma-glutamyl transpeptidaseF Pellefigue, J D Butler, S P Spielberg, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Challenges for basic research in glutaryl-CoA dehydrogenase deficiencyS Kölker, K A Strauss, S I Goodman, et al.
Biochemical and Biophysical Research Communications|July 8, 1975
Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidaseJ D Schulman, S I Goodman, J W Mace, et al.
Journal of Pediatric Surgery|October 1, 1977
Pediatric kidney transplantation for cystinosisJ C West, S I Goodman, G P Schröter, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiencyS I Goodman, E R McCabe, P V Fennessey, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Glutaric aciduria type I: outcome in the Republic of IrelandE R Naughten, P D Mayne, A A Monavari, et al.
The Journal of Pediatrics|October 1, 1976
Letter: Failure of Leucovorin therapy in nonketotic hyperglycinemiaS P Speilberg, A W Lucky, J D Schulman, et al.
The Journal of Pediatrics|October 1, 1981
Biotin-responsive in vivo carboxylase deficiency in two siblings with secretory diarrhea receiving total parenteral nutritionC L Kien, E Kohler, S I Goodman, et al.
Pageof 13

Showing results (81-90 of 130) with videos related to

Sort By:
Pageof 13
The Journal of Pediatrics|January 1, 1984
Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acidR Matalon, D A Stumpf, K Michals, et al.
Biochemical Medicine|October 1, 1982
Glutaric, 3-hydroxypropionic, and lactic aciduria with metabolic acidemia, following extensive small bowel resectionE R McCabe, S I Goodman, P V Fennessey, et al.
Biochemical and Biophysical Research Communications|December 20, 1976
Normal amino acid uptake by cultured human fibroblasts does not require gamma-glutamyl transpeptidaseF Pellefigue, J D Butler, S P Spielberg, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Challenges for basic research in glutaryl-CoA dehydrogenase deficiencyS Kölker, K A Strauss, S I Goodman, et al.
Biochemical and Biophysical Research Communications|July 8, 1975
Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidaseJ D Schulman, S I Goodman, J W Mace, et al.
Journal of Pediatric Surgery|October 1, 1977
Pediatric kidney transplantation for cystinosisJ C West, S I Goodman, G P Schröter, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiencyS I Goodman, E R McCabe, P V Fennessey, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Glutaric aciduria type I: outcome in the Republic of IrelandE R Naughten, P D Mayne, A A Monavari, et al.
The Journal of Pediatrics|October 1, 1976
Letter: Failure of Leucovorin therapy in nonketotic hyperglycinemiaS P Speilberg, A W Lucky, J D Schulman, et al.
The Journal of Pediatrics|October 1, 1981
Biotin-responsive in vivo carboxylase deficiency in two siblings with secretory diarrhea receiving total parenteral nutritionC L Kien, E Kohler, S I Goodman, et al.
Pageof 13