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Orphanet Journal of Rare Diseases|December 24, 2015
Special low protein foods for phenylketonuria: availability in Europe and an examination of their nutritional profileMaria João Pena, Manuela Ferreira Almeida, Esther van Dam, et al.
JIMD Reports|September 27, 2014
Infants with Tyrosinemia Type 1: Should phenylalanine be supplemented?Danique van Vliet, Esther van Dam, Margreet van Rijn, et al.
Journal of Inherited Metabolic Disease|November 25, 2017
Daily variation of NTBC and its relation to succinylacetone in tyrosinemia type 1 patients comparing a single dose to two doses a dayNienke S Kienstra, Hannah E van Reemst, Willem G van Ginkel, et al.
Cell Metabolism|March 21, 2020
Sugar-Induced Obesity and Insulin Resistance Are Uncoupled from Shortened Survival in DrosophilaEsther van Dam, Lucie A G van Leeuwen, Eliano Dos Santos, et al.
Neurobiology of Disease|May 5, 2015
Generation and characterization of novel conformation-specific monoclonal antibodies for α-synuclein pathologyNishant N Vaikath, Nour K Majbour, Katerina E Paleologou, et al.
Nutrients|September 14, 2024
Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria SeverityAlex Pinto, Kirsten Ahring, Manuela Ferreira Almeida, et al.
Nutrients|July 13, 2024
Blood Phenylalanine Levels in Patients with Phenylketonuria from Europe between 2012 and 2018: Is It a Changing Landscape?Alex Pinto, Kirsten Ahring, Manuela Ferreira Almeida, et al.
Nutrients|July 15, 2026
How Well Is Blood Phenylalanine Controlled in Maternal PKU in Europe? Results from 102 PregnanciesAlex Pinto, Kirsten Ahring, Manuela Ferreira Almeida, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 18, 2019
Dietary practices in methylmalonic acidaemia: a European surveyAlex Pinto, Sharon Evans, Anne Daly, et al.
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