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Nutrients|May 27, 2023
Amino Acid Analyses of Plant Foods Used in the Dietary Management of Inherited Amino Acid DisordersSuzanne Ford, Fatma Ilgaz, Sarah Hawker, et al.
The Breast Journal|November 22, 2005
Erdheim-Chester disease of the breast: a case report and review of the literaturePenny J Barnes, Annette Foyle, Kelly A Dakin Haché, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2025
Global considerations for lifelong management and therapeutic development for phenylketonuriaNicola Longo, Takashi Hamazaki, Suzanne Hollander, et al.
Orphanet Journal of Rare Diseases|October 28, 2022
Transitioning of protein substitutes in patients with phenylketonuria: evaluation of current practiceOzlem Yilmaz, Alex Pinto, Anne Daly, et al.
Molecular Genetics and Metabolism Reports|September 14, 2016
The personal burden for caregivers of children with phenylketonuria: A cross-sectional study investigating time burden and costs in the UKAnita MacDonald, T Alexander Smith, Shamika de Silva, et al.
Nutrients|September 9, 2020
The Impact of the Use of Glycomacropeptide on Satiety and Dietary Intake in PhenylketonuriaAnne Daly, Sharon Evans, Alex Pinto, et al.
The Turkish Journal of Pediatrics|December 26, 2017
A case report of a 4-year-old child with glucose-6-phosphate dehydrogenase deficiency: An evidence based approach to nutritional managementAlex Pinto, Anita MacDonald, Esmeralda Cleto, et al.
Nutrients|August 23, 2020
Preliminary Investigation to Review If a Glycomacropeptide Compared to L-Amino Acid Protein Substitute Alters the Pre- and Postprandial Amino Acid Profile in Children with PhenylketonuriaAnne Daly, Sharon Evans, Alex Pinto, et al.
Nutrients|March 3, 2019
How Does Feeding Development and Progression onto Solid Foods in PKU Compare with Non-PKU Children During Weaning?Sharon Evans, Anne Daly, Jo Wildgoose, et al.
Orphanet Journal of Rare Diseases|January 26, 2023
Phenylalanine free infant formula in the dietary management of phenylketonuriaOzlem Yilmaz, Barbara Cochrane, Jo Wildgoose, et al.
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