Elisabetta Salvatici
Milan, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 22 publications
Low bone mineralization in phenylketonuria may be due to undiagnosed metabolic acidosis.
Journal: Molecular genetics and metabolism reports
Published: March 07, 2023
Hyperphenylalaninemias genotyping: Results of over 60 years of history in Lombardy, Italy.
Journal: Endocrinology, diabetes & metabolism
Published: September 23, 2022
Breastfeeding in Phenylketonuria: Changing Modalities, Changing Perspectives.
Journal: Nutrients
Published: September 09, 2022
Caregivers' Intention to Vaccinate Their Children Under 12 Years of Age Against COVID-19: A Cross-Sectional Multi-Center Study in Milan, Italy.
Journal: Frontiers in pediatrics
Published: December 13, 2021
L-alanine supplementation in Pompe disease (IOPD): a potential therapeutic implementation for patients on ERT? A case report.
Journal: Italian journal of pediatrics
Published: September 20, 2021
Telehealth and COVID-19: Empowering Standards of Management for Patients Affected by Phenylketonuria and Hyperphenylalaninemia.
Journal: Healthcare (Basel, Switzerland)
Published: September 16, 2021
PKU and COVID19: How the pandemic changed metabolic control.
Journal: Molecular genetics and metabolism reports
Published: April 12, 2021
Retrospective analysis of 19 patients with 6-Pyruvoyl Tetrahydropterin Synthase Deficiency: Prolactin levels inversely correlate with growth.
Journal: Molecular genetics and metabolism
Published: September 11, 2020
PIGW-related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literature.
Journal: American journal of medical genetics. Part A
Published: November 26, 2019
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review.
Journal: Journal of clinical medicine
Published: March 28, 2019
Last Updated: 09/26/2026