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European Journal of Clinical Nutrition|December 2, 2010
Blood phenylalanine control in phenylketonuria: a survey of 10 European centresK Ahring, A Bélanger-Quintana, K Dokoupil, et al.
Molecular 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.
Molecular Genetics and Metabolism|December 26, 2012
Use of sapropterin in the management of phenylketonuria: seven case reportsH Gokmen Ozel, A M Lammardo, K Motzfeldt, 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.
Molecular Genetics and Metabolism|October 12, 2013
Micronutrient status in phenylketonuriaM Robert, J C Rocha, M van Rijn, et al.
Molecular Genetics and Metabolism|September 11, 2013
Main issues in micronutrient supplementation in phenylketonuriaA M Lammardo, M Robert, J C Rocha, et al.
European Journal of Clinical Nutrition|April 28, 2016
Protein substitutes for phenylketonuria in Europe: access and nutritional compositionM J Pena, M F de Almeida, E van Dam, 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|April 12, 2015
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approachA Aguiar, K Ahring, M F Almeida, et al.
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