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Melanie B Gillingham

Showing results (1-10 of 61) with videos related to

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Topics 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 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
Molecular Genetics and Metabolism|March 2, 2024
A review of fatty acid oxidation disorder mouse modelsShannon J Babcock, Sander M Houten, Melanie B Gillingham
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
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.
The Journal of Pediatrics|September 3, 2013
Association of a genetic variant of carnitine palmitoyltransferase 1A with infections in Alaska Native childrenBradford D Gessner, Melanie B Gillingham, Thalia Wood, et al.
The Journal of Pediatrics|May 28, 2014
Reply: To PMID 23992672Bradford D Gessner, Melanie B Gillingham, Thalia Wood, et al.
The Journal of Pediatrics|June 15, 2014
Reply: To PMID 23992672Bradford D Gessner, Melanie B Gillingham, Thalia Wood, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|October 22, 2002
IGF-I treatment facilitates transition from parenteral to enteral nutrition in rats with short bowel syndromeMelanie B Gillingham, Elizabeth M Dahly, Sangita G Murali, et al.
Molecular Genetics and Metabolism Reports|May 19, 2020
Nutrient intake, body composition, and blood phenylalanine control in children with phenylketonuria compared to healthy controlsMelissa Sailer, Gabriela Elizondo, Julie Martin, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Topics 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 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
Molecular Genetics and Metabolism|March 2, 2024
A review of fatty acid oxidation disorder mouse modelsShannon J Babcock, Sander M Houten, Melanie B Gillingham
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
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.
The Journal of Pediatrics|September 3, 2013
Association of a genetic variant of carnitine palmitoyltransferase 1A with infections in Alaska Native childrenBradford D Gessner, Melanie B Gillingham, Thalia Wood, et al.
The Journal of Pediatrics|May 28, 2014
Reply: To PMID 23992672Bradford D Gessner, Melanie B Gillingham, Thalia Wood, et al.
The Journal of Pediatrics|June 15, 2014
Reply: To PMID 23992672Bradford D Gessner, Melanie B Gillingham, Thalia Wood, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|October 22, 2002
IGF-I treatment facilitates transition from parenteral to enteral nutrition in rats with short bowel syndromeMelanie B Gillingham, Elizabeth M Dahly, Sangita G Murali, et al.
Molecular Genetics and Metabolism Reports|May 19, 2020
Nutrient intake, body composition, and blood phenylalanine control in children with phenylketonuria compared to healthy controlsMelissa Sailer, Gabriela Elizondo, Julie Martin, et al.
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