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JIMD Reports|July 21, 2020
Evaluation of 11 years of newborn screening for maple syrup urine disease in the Netherlands and a systematic review of the literature: Strategies for optimizationKevin Stroek, Anita Boelen, Marelle J Bouva, et al.Clinical Nutrition (Edinburgh, Scotland)|January 16, 2021
High protein prescription in methylmalonic and propionic acidemia patients and its negative association with long-term outcomeF Molema, H A Haijes, M C Janssen, et al.Journal of the American Dietetic Association|October 18, 2008
A survey of natural protein intake in Dutch phenylketonuria patients: insight into estimation or measurement of dietary intakeMargreet van Rijn, Jolanda Jansma, Aeltsje Brinksma, et al.Molecular Genetics and Metabolism|October 15, 2011
The 48-hour tetrahydrobiopterin loading test in patients with phenylketonuria: evaluation of protocol and influence of baseline phenylalanine concentrationK Anjema, G Venema, F C Hofstede, et al.Orphanet Journal of Rare Diseases|April 29, 2019
The natural history of classic galactosemia: lessons from the GalNet registryM E Rubio-Gozalbo, M Haskovic, A M Bosch, et al.Pageof 7