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Cary O Harding

Showing results (31-40 of 113) with videos related to

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Journal of Inherited Metabolic Disease|February 26, 2019
Response to Letter to the editorMelanie B Gillingham, Stephen B Heitner, Michael R Lasarev, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 26, 2008
Correction of murine PKU following AAV-mediated intramuscular expression of a complete phenylalanine hydroxylating systemZhaobing Ding, Cary O Harding, Alexandre Rebuffat, et al.
American Journal of Physiology. Endocrinology and Metabolism|September 26, 2013
Altered body composition and energy expenditure but normal glucose tolerance among humans with a long-chain fatty acid oxidation disorderMelanie B Gillingham, Cary O Harding, Dale A Schoeller, et al.
Journal of Inherited Metabolic Disease|February 4, 2014
Pharmacologic inhibition of L-tyrosine degradation ameliorates cerebral dopamine deficiency in murine phenylketonuria (PKU)Cary O Harding, Shelley R Winn, K Michael Gibson, et al.
Molecular Genetics and Metabolism|January 25, 2023
Resting and total energy expenditure of patients with long-chain fatty acid oxidation disorders (LC-FAODs)James P DeLany, Angela Horgan, Ashley Gregor, et al.
Nutrition Research (New York, N.Y.)|January 17, 2016
Normal vitamin D levels and bone mineral density among children with inborn errors of metabolism consuming medical food-based dietsKatie E Geiger, David M Koeller, Cary O Harding, et al.
Molecular Genetics and Metabolism|January 20, 2004
The fate of intravenously administered tetrahydrobiopterin and its implications for heterologous gene therapy of phenylketonuriaCary O Harding, Mark Neff, Krzysztof Wild, et al.
Molecular Genetics and Metabolism|March 31, 2012
Observations regarding retinopathy in mitochondrial trifunctional protein deficienciesAutumn L Fletcher, Mark E Pennesi, Cary O Harding, et al.
Molecular Genetics and Metabolism|September 26, 2006
Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencyMelanie B Gillingham, Jonathan Q Purnell, Julia Jordan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 27, 2005
Low therapeutic threshold for hepatocyte replacement in murine phenylketonuriaKelly Hamman, Heather Clark, Eugenio Montini, et al.
Pageof 12

Showing results (31-40 of 113) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|February 26, 2019
Response to Letter to the editorMelanie B Gillingham, Stephen B Heitner, Michael R Lasarev, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 26, 2008
Correction of murine PKU following AAV-mediated intramuscular expression of a complete phenylalanine hydroxylating systemZhaobing Ding, Cary O Harding, Alexandre Rebuffat, et al.
American Journal of Physiology. Endocrinology and Metabolism|September 26, 2013
Altered body composition and energy expenditure but normal glucose tolerance among humans with a long-chain fatty acid oxidation disorderMelanie B Gillingham, Cary O Harding, Dale A Schoeller, et al.
Journal of Inherited Metabolic Disease|February 4, 2014
Pharmacologic inhibition of L-tyrosine degradation ameliorates cerebral dopamine deficiency in murine phenylketonuria (PKU)Cary O Harding, Shelley R Winn, K Michael Gibson, et al.
Molecular Genetics and Metabolism|January 25, 2023
Resting and total energy expenditure of patients with long-chain fatty acid oxidation disorders (LC-FAODs)James P DeLany, Angela Horgan, Ashley Gregor, et al.
Nutrition Research (New York, N.Y.)|January 17, 2016
Normal vitamin D levels and bone mineral density among children with inborn errors of metabolism consuming medical food-based dietsKatie E Geiger, David M Koeller, Cary O Harding, et al.
Molecular Genetics and Metabolism|January 20, 2004
The fate of intravenously administered tetrahydrobiopterin and its implications for heterologous gene therapy of phenylketonuriaCary O Harding, Mark Neff, Krzysztof Wild, et al.
Molecular Genetics and Metabolism|March 31, 2012
Observations regarding retinopathy in mitochondrial trifunctional protein deficienciesAutumn L Fletcher, Mark E Pennesi, Cary O Harding, et al.
Molecular Genetics and Metabolism|September 26, 2006
Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencyMelanie B Gillingham, Jonathan Q Purnell, Julia Jordan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 27, 2005
Low therapeutic threshold for hepatocyte replacement in murine phenylketonuriaKelly Hamman, Heather Clark, Eugenio Montini, et al.
Pageof 12