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Journal of Inherited Metabolic Disease|May 25, 2010
Therapeutic liver repopulation for phenylketonuriaCary O Harding, K M GibsonBiologics : Targets & Therapy|August 18, 2010
New era in treatment for phenylketonuria: Pharmacologic therapy with sapropterin dihydrochlorideCary O HardingMolecular Frontiers Journal|June 12, 2020
Prospects for Cell-Directed Curative Therapy of Phenylketonuria (PKU)Cary O HardingFree Radical Biology & Medicine|May 22, 2003
L-2-oxothiazolidine-4-carboxylate supplementation in murine gamma-GT deficiencyPatrice Held, Cary O HardingMolecular Genetics and Metabolism|January 20, 2004
State-of-the-art 2003 on PKU gene therapyZhaobing Ding, Cary O Harding, Beat ThönyTopics in Clinical Nutrition|July 1, 2010
EFFECT OF FEEDING, EXERCISE AND GENOTYPE ON PLASMA 3-HYDROXYACYLCARNITINES IN CHILDREN WITH LCHAD DEFICIENCYMelanie B Gillingham, Dietrich Matern, Cary O HardingMolecular 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 HardingTopics in Clinical Nutrition|December 17, 2009
NORMAL FATTY ACID CONCENTRATIONS IN YOUNG CHILDREN WITH PHENYLKETONURIA (PKU)Stacey M Lavoie, Cary O Harding, Melanie B GillinghamSouthern Medical Journal|April 17, 2008
Postchemotherapy hyperammonemic encephalopathy emulating ornithine transcarbamoylase (OTC) deficiencyJoseph S Chan, Cary O Harding, Charles D BlankeHuman 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.Pageof 25