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L Sweetman

Showing results (101-110 of 175) with videos related to

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Annals of the New York Academy of Sciences|January 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatmentD M Mock, D L Baswell, H Baker, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
3-Ketothiolase deficiency: heterogeneity in a defect of mitochondrial acetoacetyl-CoA thiolase biosynthesis in fibroblasts from four patientsH Nagasawa, S Yamaguchi, T Orii, et al.
European Journal of Pediatrics|September 1, 1984
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyW G Wilson, M B Cass, O Søvik, et al.
Biophysical Journal|May 12, 2009
Nature of the individual Ca binding sites in Ca-regenerated bacteriorhodopsinY N Zhang, L L Sweetman, E S Awad, et al.
American Journal of Medical Genetics|April 1, 1990
Pyridoxine-unresponsive homocystinuria with an unusual clinical courseF B Cochran, L Sweetman, K Schmidt, et al.
The New England Journal of Medicine|April 2, 1981
Biotin deficiency: an unusual complication of parenteral alimentationD M Mock, A A deLorimer, W M Liebman, et al.
The Journal of Pediatrics|May 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatmentD M Mock, D L Baswell, H Baker, et al.
Pediatric Research|August 1, 1979
Abnormal pyruvate and alpha-ketoglutarate dehydrogenase complexes in a patient with lactic acidemiaY Kuroda, J J Kline, L Sweetman, et al.
The Journal of Pediatrics|June 1, 1980
Glutaric aciduria Type IIL Sweetman, W L Nyhan, D A Tauner, et al.
Monographs in Human Genetics|January 1, 1978
The diagnosis and management of propionic acidemiaC de Cespedes, A R Loria, Y Estrada, et al.
Pageof 18

Showing results (101-110 of 175) with videos related to

Sort By:
Pageof 18
Annals of the New York Academy of Sciences|January 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatmentD M Mock, D L Baswell, H Baker, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
3-Ketothiolase deficiency: heterogeneity in a defect of mitochondrial acetoacetyl-CoA thiolase biosynthesis in fibroblasts from four patientsH Nagasawa, S Yamaguchi, T Orii, et al.
European Journal of Pediatrics|September 1, 1984
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyW G Wilson, M B Cass, O Søvik, et al.
Biophysical Journal|May 12, 2009
Nature of the individual Ca binding sites in Ca-regenerated bacteriorhodopsinY N Zhang, L L Sweetman, E S Awad, et al.
American Journal of Medical Genetics|April 1, 1990
Pyridoxine-unresponsive homocystinuria with an unusual clinical courseF B Cochran, L Sweetman, K Schmidt, et al.
The New England Journal of Medicine|April 2, 1981
Biotin deficiency: an unusual complication of parenteral alimentationD M Mock, A A deLorimer, W M Liebman, et al.
The Journal of Pediatrics|May 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatmentD M Mock, D L Baswell, H Baker, et al.
Pediatric Research|August 1, 1979
Abnormal pyruvate and alpha-ketoglutarate dehydrogenase complexes in a patient with lactic acidemiaY Kuroda, J J Kline, L Sweetman, et al.
The Journal of Pediatrics|June 1, 1980
Glutaric aciduria Type IIL Sweetman, W L Nyhan, D A Tauner, et al.
Monographs in Human Genetics|January 1, 1978
The diagnosis and management of propionic acidemiaC de Cespedes, A R Loria, Y Estrada, et al.
Pageof 18