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Molecular Genetics and Metabolism Reports|August 21, 2023
Low bone mineralization in phenylketonuria may be due to undiagnosed metabolic acidosisValentina Rovelli, Vittoria Ercoli, Alice Re Dionigi, et al.
Nutrients|October 14, 2022
Breastfeeding in Phenylketonuria: Changing Modalities, Changing PerspectivesJuri Zuvadelli, Sabrina Paci, Elisabetta Salvatici, et al.
Nutrients|August 30, 2018
Exploring Drivers of Liking of Low-Phenylalanine Products in Subjects with Phenyilketonuria Using Check-All-That-Apply MethodCristina Proserpio, Ella Pagliarini, Juri Zuvadelli, et al.
Nutrients|January 28, 2026
The First 1000 Days of PKU: A Narrative Review of Maternal PKU and Early Life Management After Positive Newborn ScreeningElvira Verduci, Martina Tosi, Juri Zuvadelli, et al.
Healthcare (Basel, Switzerland)|November 27, 2021
Telehealth and COVID-19: Empowering Standards of Management for Patients Affected by Phenylketonuria and HyperphenylalaninemiaValentina Rovelli, Juri Zuvadelli, Sabrina Paci, et al.
Orphanet Journal of Rare Diseases|November 17, 2021
Italian national consensus statement on management and pharmacological treatment of phenylketonuriaAlberto Burlina, Giacomo Biasucci, Maria Teresa Carbone, et al.
Molecular Genetics and Metabolism|March 24, 2024
Pegvaliase therapy for phenylketonuria: Real-world case series and clinical insightsIris Scala, Lucia Brodosi, Daniela Gueraldi, et al.
Nutrients|May 14, 2022
Glycomacropeptide Safety and Its Effect on Gut Microbiota in Patients with Phenylketonuria: A Pilot StudyChiara Montanari, Camilla Ceccarani, Antonio Corsello, et al.
Italian Journal of Pediatrics|March 29, 2022
L-alanine supplementation in Pompe disease (IOPD): a potential therapeutic implementation for patients on ERT? A case reportValentina Rovelli, Juri Zuvadelli, Marta Piotto, et al.
Molecular Genetics and Metabolism Reports|April 28, 2021
PKU and COVID19: How the pandemic changed metabolic controlValentina Rovelli, Juri Zuvadelli, Vittoria Ercoli, et al.
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