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Rani H Singh

Showing results (1-10 of 65) with videos related to

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Molecular Genetics and Metabolism|October 16, 2021
Natural history of children and adults with phenylketonuria in the NBS-PKU Connect registryAileen Kenneson, Rani H Singh
Orphanet Journal of Rare Diseases|October 10, 2020
Presentation and management of N-acetylglutamate synthase deficiency: a review of the literatureAileen Kenneson, Rani H Singh
The American Journal of Clinical Nutrition|December 5, 2021
Plasma metabolomic profile changes in females with phenylketonuria following a camp interventionMeriah S Schoen, Rani H Singh
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2010
Newborn dried bloodspot screening: long-term follow-up activities and information system requirementsRani H Singh, Alan R Hinman
Molecular Genetics and Metabolism|October 12, 2011
Using change in plasma phenylalanine concentrations and ability to liberalize diet to classify responsiveness to tetrahydrobiopterin therapy in patients with phenylketonuriaRani H Singh, Meghan E Quirk
Journal of the American Dietetic Association|December 19, 2002
Management of fatty acid oxidation disorders: a survey of current treatment strategiesJava O Solis, Rani H Singh
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2008
Standards of professional practice for genetic metabolic dietitiansRani H Singh, Melissa M Kaczmarczyk
Molecular Genetics and Metabolism Reports|August 11, 2020
Genetic testing experiences and genetics knowledge among families with inherited metabolic diseasesAileen Kenneson, Lauren Youngborg, Rani H Singh
The Cochrane Database of Systematic Reviews|February 28, 2015
Protein substitute for children and adults with phenylketonuriaSarah H L Yi, Rani H Singh
The Cochrane Database of Systematic Reviews|October 10, 2008
Protein substitute for children and adults with phenylketonuriaSarah H L Yi, Rani H Singh
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Molecular Genetics and Metabolism|October 16, 2021
Natural history of children and adults with phenylketonuria in the NBS-PKU Connect registryAileen Kenneson, Rani H Singh
Orphanet Journal of Rare Diseases|October 10, 2020
Presentation and management of N-acetylglutamate synthase deficiency: a review of the literatureAileen Kenneson, Rani H Singh
The American Journal of Clinical Nutrition|December 5, 2021
Plasma metabolomic profile changes in females with phenylketonuria following a camp interventionMeriah S Schoen, Rani H Singh
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2010
Newborn dried bloodspot screening: long-term follow-up activities and information system requirementsRani H Singh, Alan R Hinman
Molecular Genetics and Metabolism|October 12, 2011
Using change in plasma phenylalanine concentrations and ability to liberalize diet to classify responsiveness to tetrahydrobiopterin therapy in patients with phenylketonuriaRani H Singh, Meghan E Quirk
Journal of the American Dietetic Association|December 19, 2002
Management of fatty acid oxidation disorders: a survey of current treatment strategiesJava O Solis, Rani H Singh
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2008
Standards of professional practice for genetic metabolic dietitiansRani H Singh, Melissa M Kaczmarczyk
Molecular Genetics and Metabolism Reports|August 11, 2020
Genetic testing experiences and genetics knowledge among families with inherited metabolic diseasesAileen Kenneson, Lauren Youngborg, Rani H Singh
The Cochrane Database of Systematic Reviews|February 28, 2015
Protein substitute for children and adults with phenylketonuriaSarah H L Yi, Rani H Singh
The Cochrane Database of Systematic Reviews|October 10, 2008
Protein substitute for children and adults with phenylketonuriaSarah H L Yi, Rani H Singh
Pageof 7