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P Rinaldo

Showing results (21-30 of 95) with videos related to

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Clinical Chemistry|November 9, 2000
Methylmalonic acid measured in plasma and urine by stable-isotope dilution and electrospray tandem mass spectrometryM J Magera, J K Helgeson, D Matern, et al.
Biochemical and Biophysical Research Communications|April 6, 1995
Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunitM J Weinberger, P Rinaldo, A W Strauss, et al.
Biology of the Neonate|January 1, 1987
Carnitine and the prematureF F Rubaltelli, A Orzali, P Rinaldo, et al.
The Journal of Pediatrics|March 1, 1992
Intentional infantile ethylene glycol poisoning presenting as an inherited metabolic disorderA D Woolf, A Wynshaw-Boris, P Rinaldo, et al.
Biological Mass Spectrometry|August 1, 1991
Mass spectrometric analysis of metabolite excretion in five Japanese patients with the late-onset form of glutaric aciduria type IIN Shimizu, S Yamaguchi, T Orii, et al.
Human Pathology|August 1, 1994
Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liverR G Boles, S K Martin, M G Blitzer, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypesX Fu, P Rinaldo, S H Hahn, et al.
Molecular Genetics and Metabolism|September 26, 2000
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathwaysJ Vockley, P Rinaldo, M J Bennett, et al.
The Journal of Pediatrics|September 1, 1996
Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapyM H Fries, P Rinaldo, E Schmidt-Sommerfeld, et al.
Progress in Clinical and Biological Research|January 1, 1992
The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase geneI Yokota, P M Coates, D E Hale, et al.
Pageof 10

Showing results (21-30 of 95) with videos related to

Sort By:
Pageof 10
Clinical Chemistry|November 9, 2000
Methylmalonic acid measured in plasma and urine by stable-isotope dilution and electrospray tandem mass spectrometryM J Magera, J K Helgeson, D Matern, et al.
Biochemical and Biophysical Research Communications|April 6, 1995
Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunitM J Weinberger, P Rinaldo, A W Strauss, et al.
Biology of the Neonate|January 1, 1987
Carnitine and the prematureF F Rubaltelli, A Orzali, P Rinaldo, et al.
The Journal of Pediatrics|March 1, 1992
Intentional infantile ethylene glycol poisoning presenting as an inherited metabolic disorderA D Woolf, A Wynshaw-Boris, P Rinaldo, et al.
Biological Mass Spectrometry|August 1, 1991
Mass spectrometric analysis of metabolite excretion in five Japanese patients with the late-onset form of glutaric aciduria type IIN Shimizu, S Yamaguchi, T Orii, et al.
Human Pathology|August 1, 1994
Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liverR G Boles, S K Martin, M G Blitzer, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypesX Fu, P Rinaldo, S H Hahn, et al.
Molecular Genetics and Metabolism|September 26, 2000
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathwaysJ Vockley, P Rinaldo, M J Bennett, et al.
The Journal of Pediatrics|September 1, 1996
Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapyM H Fries, P Rinaldo, E Schmidt-Sommerfeld, et al.
Progress in Clinical and Biological Research|January 1, 1992
The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase geneI Yokota, P M Coates, D E Hale, et al.
Pageof 10