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Cary O Harding

Showing results (11-20 of 113) with videos related to

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Molecular Genetics and Metabolism|September 16, 2011
Hepatocytes from wild-type or heterozygous donors are equally effective in achieving successful therapeutic liver repopulation in murine phenylketonuria (PKU)Kelly J Hamman, Shelley R Winn, Cary O Harding
Topics in Clinical Nutrition|December 17, 2009
NORMAL FATTY ACID CONCENTRATIONS IN YOUNG CHILDREN WITH PHENYLKETONURIA (PKU)Stacey M Lavoie, Cary O Harding, Melanie B Gillingham
Southern Medical Journal|April 17, 2008
Postchemotherapy hyperammonemic encephalopathy emulating ornithine transcarbamoylase (OTC) deficiencyJoseph S Chan, Cary O Harding, Charles D Blanke
Human Gene Therapy|November 18, 2009
Comparison of adeno-associated virus pseudotype 1, 2, and 8 vectors administered by intramuscular injection in the treatment of murine phenylketonuriaAlexandre Rebuffat, Cary O Harding, Zhaobing Ding, et al.
Molecular Genetics and Metabolism|May 1, 2014
Use of propofol for short duration procedures in children with long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficienciesJulie M Martin, Melanie B Gillingham, Cary O Harding
Journal of Inherited Metabolic Disease|July 4, 2023
State-of-the-art 2023 on gene therapy for phenylketonuriaMichael Martinez, Cary O Harding, Gerald Schwank, et al.
Molecular Genetics and Metabolism|August 1, 2006
Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencyMelanie B Gillingham, Bradley Scott, Diane Elliott, et al.
Molecular Genetics and Metabolism|December 15, 2015
High dose sapropterin dihydrochloride therapy improves monoamine neurotransmitter turnover in murine phenylketonuria (PKU)Shelley R Winn, Tanja Scherer, Beat Thöny, et al.
Clinical Pediatrics|May 10, 2002
L-carnitine administration reduces number of episodes in cyclic vomiting syndromeSandra C Van Calcar, Cary O Harding, Jon A Wolff
Molecular Genetics and Metabolism|July 26, 2005
Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 genePaul J Isackson, Heather Bujnicki, Cary O Harding, et al.
Pageof 12

Showing results (11-20 of 113) with videos related to

Sort By:
Pageof 12
Molecular Genetics and Metabolism|September 16, 2011
Hepatocytes from wild-type or heterozygous donors are equally effective in achieving successful therapeutic liver repopulation in murine phenylketonuria (PKU)Kelly J Hamman, Shelley R Winn, Cary O Harding
Topics in Clinical Nutrition|December 17, 2009
NORMAL FATTY ACID CONCENTRATIONS IN YOUNG CHILDREN WITH PHENYLKETONURIA (PKU)Stacey M Lavoie, Cary O Harding, Melanie B Gillingham
Southern Medical Journal|April 17, 2008
Postchemotherapy hyperammonemic encephalopathy emulating ornithine transcarbamoylase (OTC) deficiencyJoseph S Chan, Cary O Harding, Charles D Blanke
Human Gene Therapy|November 18, 2009
Comparison of adeno-associated virus pseudotype 1, 2, and 8 vectors administered by intramuscular injection in the treatment of murine phenylketonuriaAlexandre Rebuffat, Cary O Harding, Zhaobing Ding, et al.
Molecular Genetics and Metabolism|May 1, 2014
Use of propofol for short duration procedures in children with long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficienciesJulie M Martin, Melanie B Gillingham, Cary O Harding
Journal of Inherited Metabolic Disease|July 4, 2023
State-of-the-art 2023 on gene therapy for phenylketonuriaMichael Martinez, Cary O Harding, Gerald Schwank, et al.
Molecular Genetics and Metabolism|August 1, 2006
Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencyMelanie B Gillingham, Bradley Scott, Diane Elliott, et al.
Molecular Genetics and Metabolism|December 15, 2015
High dose sapropterin dihydrochloride therapy improves monoamine neurotransmitter turnover in murine phenylketonuria (PKU)Shelley R Winn, Tanja Scherer, Beat Thöny, et al.
Clinical Pediatrics|May 10, 2002
L-carnitine administration reduces number of episodes in cyclic vomiting syndromeSandra C Van Calcar, Cary O Harding, Jon A Wolff
Molecular Genetics and Metabolism|July 26, 2005
Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 genePaul J Isackson, Heather Bujnicki, Cary O Harding, et al.
Pageof 12