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P Rinaldo

Showing results (51-60 of 95) with videos related to

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Pediatrics|July 4, 2001
Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening cardJ C Wood, M J Magera, P Rinaldo, et al.
Annals of Neurology|November 1, 1993
Short-term response to dietary therapy in molybdenum cofactor deficiencyR G Boles, L R Ment, M S Meyn, et al.
Molecular Genetics and Metabolism|May 15, 2001
Quantitative determination of plasma c8-c26 total fatty acids for the biochemical diagnosis of nutritional and metabolic disordersS A Lagerstedt, D R Hinrichs, S M Batt, et al.
Progress in Clinical and Biological Research|January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidationE Schmidt-Sommerfeld, D Penn, M Duran, et al.
Clinical Chemistry|August 1, 1995
Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bileM S Rashed, P T Ozand, M J Bennett, et al.
The Journal of Pediatrics|April 1, 1993
Effect of treatment with glycine and L-carnitine in medium-chain acyl-coenzyme A dehydrogenase deficiencyP Rinaldo, E Schmidt-Sommerfeld, A P Posca, et al.
Pediatric Research|June 1, 1992
Urinary medium-chain acylcarnitines in medium-chain acyl-CoA dehydrogenase deficiency, medium-chain triglyceride feeding and valproic acid therapy: sensitivity and specificity of the radioisotopic exchange/high performance liquid chromatography methodE Schmidt-Sommerfeld, D Penn, P Rinaldo, et al.
Circulation|March 17, 1999
Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden deathA Mathur, H F Sims, D Gopalakrishnan, et al.
Molecular Genetics and Metabolism|June 3, 2004
Rapid, comprehensive screening of the human medium chain acyl-CoA dehydrogenase geneJ T McKinney, N Longo, S H Hahn, et al.
The New England Journal of Medicine|June 3, 1999
A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant womenJ A Ibdah, M J Bennett, P Rinaldo, et al.
Pageof 10

Showing results (51-60 of 95) with videos related to

Sort By:
Pageof 10
Pediatrics|July 4, 2001
Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening cardJ C Wood, M J Magera, P Rinaldo, et al.
Annals of Neurology|November 1, 1993
Short-term response to dietary therapy in molybdenum cofactor deficiencyR G Boles, L R Ment, M S Meyn, et al.
Molecular Genetics and Metabolism|May 15, 2001
Quantitative determination of plasma c8-c26 total fatty acids for the biochemical diagnosis of nutritional and metabolic disordersS A Lagerstedt, D R Hinrichs, S M Batt, et al.
Progress in Clinical and Biological Research|January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidationE Schmidt-Sommerfeld, D Penn, M Duran, et al.
Clinical Chemistry|August 1, 1995
Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bileM S Rashed, P T Ozand, M J Bennett, et al.
The Journal of Pediatrics|April 1, 1993
Effect of treatment with glycine and L-carnitine in medium-chain acyl-coenzyme A dehydrogenase deficiencyP Rinaldo, E Schmidt-Sommerfeld, A P Posca, et al.
Pediatric Research|June 1, 1992
Urinary medium-chain acylcarnitines in medium-chain acyl-CoA dehydrogenase deficiency, medium-chain triglyceride feeding and valproic acid therapy: sensitivity and specificity of the radioisotopic exchange/high performance liquid chromatography methodE Schmidt-Sommerfeld, D Penn, P Rinaldo, et al.
Circulation|March 17, 1999
Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden deathA Mathur, H F Sims, D Gopalakrishnan, et al.
Molecular Genetics and Metabolism|June 3, 2004
Rapid, comprehensive screening of the human medium chain acyl-CoA dehydrogenase geneJ T McKinney, N Longo, S H Hahn, et al.
The New England Journal of Medicine|June 3, 1999
A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant womenJ A Ibdah, M J Bennett, P Rinaldo, et al.
Pageof 10