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C R Roe

Showing results (61-70 of 122) with videos related to

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Kidney International|May 1, 1981
Urine and serum lactic dehydrogenase, lactic dehydrogenase isoenzymes, and alkaline phosphatase in the nephrotic syndromeC B Murdock, P J Baker, E DeLong, et al.
Biochimica Et Biophysica Acta|December 31, 1997
Phytanic acid alpha-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Analytical Chemistry|November 1, 1986
Differentiation of isomeric acylcarnitines using tandem mass spectrometryS J Gaskell, C Guenat, D S Millington, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 3, 2001
Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotypeD S Roe, C Vianey-Saban, S Sharma, et al.
American Journal of Human Genetics|January 1, 1992
Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiencyJ H Ding, B Z Yang, Y Bao, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysisN M Verhoeven, C Jakobs, H J ten Brink, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Short-chain acyl-CoA dehydrogenase deficiency in a 16-year-old girl with severe muscle wasting and scoliosisK E Baerlocher, B Steinmann, A Aguzzi, et al.
The Journal of Clinical Investigation|June 1, 1984
L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemiaC R Roe, D S Millington, D A Maltby, et al.
Molecular Genetics and Metabolism|January 16, 1999
Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolismC R Roe, S D Cederbaum, D S Roe, et al.
The New England Journal of Medicine|August 30, 1990
Amelioration of proximal renal tubular dysfunction in type I glycogen storage disease with dietary therapyY T Chen, J I Scheinman, H K Park, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Kidney International|May 1, 1981
Urine and serum lactic dehydrogenase, lactic dehydrogenase isoenzymes, and alkaline phosphatase in the nephrotic syndromeC B Murdock, P J Baker, E DeLong, et al.
Biochimica Et Biophysica Acta|December 31, 1997
Phytanic acid alpha-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Analytical Chemistry|November 1, 1986
Differentiation of isomeric acylcarnitines using tandem mass spectrometryS J Gaskell, C Guenat, D S Millington, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 3, 2001
Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotypeD S Roe, C Vianey-Saban, S Sharma, et al.
American Journal of Human Genetics|January 1, 1992
Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiencyJ H Ding, B Z Yang, Y Bao, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysisN M Verhoeven, C Jakobs, H J ten Brink, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Short-chain acyl-CoA dehydrogenase deficiency in a 16-year-old girl with severe muscle wasting and scoliosisK E Baerlocher, B Steinmann, A Aguzzi, et al.
The Journal of Clinical Investigation|June 1, 1984
L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemiaC R Roe, D S Millington, D A Maltby, et al.
Molecular Genetics and Metabolism|January 16, 1999
Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolismC R Roe, S D Cederbaum, D S Roe, et al.
The New England Journal of Medicine|August 30, 1990
Amelioration of proximal renal tubular dysfunction in type I glycogen storage disease with dietary therapyY T Chen, J I Scheinman, H K Park, et al.
Pageof 13