Zuvadelli J - Search Results

1

L-alanine supplementation in Pompe disease (IOPD): a potential therapeutic implementation for patients on ERT? A case report.

Rovelli V, Zuvadelli J, Piotto M, Scopari A, Dionigi AR, Ercoli V, Paci S, Cefalo G, Salvatici E, Banderali G. Rovelli V, et al. Among authors: zuvadelli j. Ital J Pediatr. 2022 Mar 28;48(1):48. doi: 10.1186/s13052-022-01249-y. Ital J Pediatr. 2022. PMID: 35346323 Free PMC article.

2

Exploring Drivers of Liking of Low-Phenylalanine Products in Subjects with Phenyilketonuria Using Check-All-That-Apply Method.

Proserpio C, Pagliarini E, Zuvadelli J, Paci S, Re Dionigi A, Banderali G, Cattaneo C, Verduci E. Proserpio C, et al. Among authors: zuvadelli j. Nutrients. 2018 Aug 28;10(9):1179. doi: 10.3390/nu10091179. Nutrients. 2018. PMID: 30154357 Free PMC article.

3

PKU and COVID19: How the pandemic changed metabolic control.

Rovelli V, Zuvadelli J, Ercoli V, Montanari C, Paci S, Dionigi AR, Scopari A, Salvatici E, Cefalo G, Banderali G. Rovelli V, et al. Among authors: zuvadelli j. Mol Genet Metab Rep. 2021 Jun;27:100759. doi: 10.1016/j.ymgmr.2021.100759. Epub 2021 Apr 23. Mol Genet Metab Rep. 2021. PMID: 33907667 Free PMC article.

4

Italian national consensus statement on management and pharmacological treatment of phenylketonuria.

Burlina A, Biasucci G, Carbone MT, Cazzorla C, Paci S, Pochiero F, Spada M, Tummolo A, Zuvadelli J, Leuzzi V. Burlina A, et al. Among authors: zuvadelli j. Orphanet J Rare Dis. 2021 Nov 16;16(1):476. doi: 10.1186/s13023-021-02086-8. Orphanet J Rare Dis. 2021. PMID: 34784942 Free PMC article.

5

Telehealth and COVID-19: Empowering Standards of Management for Patients Affected by Phenylketonuria and Hyperphenylalaninemia.

Rovelli V, Zuvadelli J, Paci S, Ercoli V, Re Dionigi A, Selmi R, Salvatici E, Cefalo G, Banderali G. Rovelli V, et al. Among authors: zuvadelli j. Healthcare (Basel). 2021 Oct 20;9(11):1407. doi: 10.3390/healthcare9111407. Healthcare (Basel). 2021. PMID: 34828453 Free PMC article.

6

Glycomacropeptide Safety and Its Effect on Gut Microbiota in Patients with Phenylketonuria: A Pilot Study.

Montanari C, Ceccarani C, Corsello A, Zuvadelli J, Ottaviano E, Dei Cas M, Banderali G, Zuccotti G, Borghi E, Verduci E. Montanari C, et al. Among authors: zuvadelli j. Nutrients. 2022 Apr 29;14(9):1883. doi: 10.3390/nu14091883. Nutrients. 2022. PMID: 35565850 Free PMC article.

7

Breastfeeding in Phenylketonuria: Changing Modalities, Changing Perspectives.

Zuvadelli J, Paci S, Salvatici E, Giorgetti F, Cefalo G, Re Dionigi A, Rovelli V, Banderali G. Zuvadelli J, et al. Nutrients. 2022 Oct 5;14(19):4138. doi: 10.3390/nu14194138. Nutrients. 2022. PMID: 36235790 Free PMC article.

8

Hyperphenylalaninemias genotyping: Results of over 60 years of history in Lombardy, Italy.

Rovelli V, Cefalo G, Ercoli V, Zuvadelli J, Olivia T, Graziani D, Luisella A, Bassi D, Re Dionigi A, Selmi R, Paci S, Salvatici E, Banderali G. Rovelli V, et al. Among authors: zuvadelli j. Endocrinol Diabetes Metab. 2023 Mar;6(2):e396. doi: 10.1002/edm2.396. Epub 2022 Dec 19. Endocrinol Diabetes Metab. 2023. PMID: 36537053 Free PMC article.

9

Low bone mineralization in phenylketonuria may be due to undiagnosed metabolic acidosis.

Rovelli V, Ercoli V, Dionigi AR, Paci S, Salvatici E, Zuvadelli J, Banderali G. Rovelli V, et al. Among authors: zuvadelli j. Mol Genet Metab Rep. 2023 Aug 9;36:100998. doi: 10.1016/j.ymgmr.2023.100998. eCollection 2023 Sep. Mol Genet Metab Rep. 2023. PMID: 37600232 Free PMC article.

10

Dysbiosis, Host Metabolism, and Non-communicable Diseases: Trialogue in the Inborn Errors of Metabolism.

Montanari C, Parolisi S, Borghi E, Putignani L, Bassanini G, Zuvadelli J, Bonfanti C, Tummolo A, Dionisi Vici C, Biasucci G, Burlina A, Carbone MT, Verduci E. Montanari C, et al. Among authors: zuvadelli j. Front Physiol. 2021 Sep 6;12:716520. doi: 10.3389/fphys.2021.716520. eCollection 2021. Front Physiol. 2021. PMID: 34588993 Free PMC article. Review.

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