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Drugs of Today (Barcelona, Spain : 1998)|September 11, 2010
Sapropterin dihydrochloride: a new drug and a new concept in the management of phenylketonuriaF K Trefz, A Belanger-QuintanaMolecular Genetics and Metabolism|January 6, 2012
Diet in phenylketonuria: a snapshot of special dietary costs and reimbursement systems in 10 international centersA Belanger-Quintana, K Dokoupil, H Gokmen-Ozel, et al.Orphanet Journal of Rare Diseases|August 4, 2025
Multicenter study on long-term growth in patients with phenylketonuriaS Stanescu, A Belanger-Quintana, J C Rocha, et al.Journal of Inherited Metabolic Disease|August 15, 2006
Persistent increase of plasma butyryl/isobutyrylcarnitine concentrations as marker of SCAD defect and ethylmalonic encephalopathyB Merinero, C Pérez-Cerdá, P Ruiz Sala, et al.JIMD Reports|July 30, 2017
Four Years' Experience in the Diagnosis of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency in Infants Detected in Three Spanish Newborn Screening CentersB Merinero, P Alcaide, E Martín-Hernández, et al.Molecular Genetics and Metabolism|October 27, 2015
The challenges of managing coexistent disorders with phenylketonuria: 30 casesA MacDonald, K Ahring, M F Almeida, et al.Molecular Genetics and Metabolism Reports|March 10, 2017
Dietary practices in isovaleric acidemia: A European surveyA Pinto, A Daly, S Evans, et al.Molecular Genetics and Metabolism Reports|October 13, 2017
Dietary practices in propionic acidemia: A European surveyA Daly, A Pinto, S Evans, et al.Molecular Genetics and Metabolism|April 12, 2015
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approachA Aguiar, K Ahring, M F Almeida, et al.Molecular Genetics and Metabolism Reports|February 2, 2019
Weaning practices in phenylketonuria vary between health professionals in EuropeA Pinto, S Adams, K Ahring, et al.Pageof 2