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Nutrition & Metabolism|February 7, 2012
Phenylketonuria: nutritional advances and challengesMarcello Giovannini, Elvira Verduci, Elisabetta Salvatici, et al.Current Medical Research and Opinion|November 23, 2020
The management of phenylketonuria in adult patients in Italy: a survey of six specialist metabolic centersAlberto Burlina, Vincenzo Leuzzi, Marco Spada, et al.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.JIMD Reports|December 24, 2013
Quality of life in adult patients with glycogen storage disease type I: results of a multicenter italian studyAnnalisa Sechi, Laura Deroma, Sabrina Paci, 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.Scandinavian Journal of Clinical and Laboratory Investigation|October 25, 2011
Erythrocyte Galactose-1-phosphate measurement by GC-MS in the monitoring of classical galactosemiaGiuliana Cangemi, Sebastiano Barco, Laura Barbagallo, et al.Journal of Inherited Metabolic Disease|May 8, 2012
Fertility and pregnancy in women affected by glycogen storage disease type I, results of a multicenter Italian studyAnnalisa Sechi, Laura Deroma, Annunziata Lapolla, 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.Metabolic Brain Disease|July 4, 2019
Novel mutations in two unrelated Italian patients with SSADH deficiencyMarta Balzarini, Valentina Rovelli, Sabrina Paci, et al.Pageof 4