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Nutricion Hospitalaria|March 23, 2018
[3-hydroxy-3-methylglutaryl-CoA lyase deficiency: a case report and literature review]Ozlem Yilmaz, Steve Kitchen, Alex Pinto, et al.
Molecular Genetics and Metabolism|October 24, 2022
Altered gut microbiome diversity and function in patients with propionic acidemiaSebastian Tims, Cyril Marsaux, Alex Pinto, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 10, 2018
The safety of Lipistart, a medium-chain triglyceride based formula, in the dietary treatment of long-chain fatty acid disorders: a phase I studyAnita MacDonald, Rachel Webster, Matthew Whitlock, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
When should social service referral be considered in phenylketonuria?Margreet van Rijn, Kirsten Ahring, Amaya Bélanger-Quintana, et al.
Orphanet Journal of Rare Diseases|January 16, 2014
Single amino acid supplementation in aminoacidopathies: a systematic reviewDanique van Vliet, Terry G J Derks, Margreet van Rijn, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|March 6, 2022
Dietary treatment in Dutch children with phenylketonuria: An inventory of associated social restrictions and eating problemsSietske Haitjema, Charlotte M A Lubout, David Abeln, et al.
Nutrients|December 11, 2025
Point-of-Care Testing in PKU: A New ERA of Blood Phenylalanine MonitoringAlex Pinto, Adam Gerrard, Suresh Vijay, et al.
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