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C R Roe

Showing results (91-100 of 122) with videos related to

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Circulation|July 1, 1973
Recognition of postoperative acute myocardial infarction. Application of isoenzyme techniquesS H Dixon, L E Limbird, C R Roe, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1992
Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavinW J Triggs, C R Roe, W J Rhead, et al.
Archives of Disease in Childhood|November 1, 1983
Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groupsC R Roe, C L Hoppel, T E Stacey, et al.
Pediatrics|July 1, 1985
Creatine kinase brain isoenzyme: relationship of cerebrospinal fluid concentration to the neurologic condition of newborns and cellular localization in the human brainG Worley, B Lipman, I H Gewolb, et al.
Progress in Clinical and Biological Research|January 1, 1992
The role of tandem mass spectrometry in the diagnosis of fatty acid oxidation disordersD S Millington, N Terada, D H Chace, et al.
The Journal of Pediatrics|January 1, 1988
Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuriaD W Bartholomew, M L Batshaw, R H Allen, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, C Vianey-Saban, P Bross, et al.
Biochemical and Molecular Medicine|June 1, 1996
Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathyM C Brown-Harrison, M A Nada, H Sprecher, et al.
Molecular Genetics and Metabolism|April 18, 2000
Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyB Z Yang, J H Ding, C Zhou, et al.
Progress in Clinical and Biological Research|January 1, 1990
The L-3-hydroxyacyl-CoA dehydrogenase deficiencyD E Hale, C Thorpe, K Braat, et al.
Pageof 13

Showing results (91-100 of 122) with videos related to

Sort By:
Pageof 13
Circulation|July 1, 1973
Recognition of postoperative acute myocardial infarction. Application of isoenzyme techniquesS H Dixon, L E Limbird, C R Roe, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1992
Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavinW J Triggs, C R Roe, W J Rhead, et al.
Archives of Disease in Childhood|November 1, 1983
Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groupsC R Roe, C L Hoppel, T E Stacey, et al.
Pediatrics|July 1, 1985
Creatine kinase brain isoenzyme: relationship of cerebrospinal fluid concentration to the neurologic condition of newborns and cellular localization in the human brainG Worley, B Lipman, I H Gewolb, et al.
Progress in Clinical and Biological Research|January 1, 1992
The role of tandem mass spectrometry in the diagnosis of fatty acid oxidation disordersD S Millington, N Terada, D H Chace, et al.
The Journal of Pediatrics|January 1, 1988
Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuriaD W Bartholomew, M L Batshaw, R H Allen, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, C Vianey-Saban, P Bross, et al.
Biochemical and Molecular Medicine|June 1, 1996
Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathyM C Brown-Harrison, M A Nada, H Sprecher, et al.
Molecular Genetics and Metabolism|April 18, 2000
Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyB Z Yang, J H Ding, C Zhou, et al.
Progress in Clinical and Biological Research|January 1, 1990
The L-3-hydroxyacyl-CoA dehydrogenase deficiencyD E Hale, C Thorpe, K Braat, et al.
Pageof 13