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Orphanet Journal of Rare Diseases|June 20, 2022
Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XIMiriam Massese, Francesco Tagliaferri, Carlo Dionisi-Vici, et al.
JMIR Pediatrics and Parenting|June 3, 2021
A Global Overview of COVID-19 Research in the Pediatric Field: Bibliometric ReviewAlice Monzani, Francesco Tagliaferri, Simonetta Bellone, et al.
Minerva Pediatrica|June 9, 2020
Vitamin D effects and endocrine diseasesSilvia Savastio, Roberta Cinquatti, Francesco Tagliaferri, et al.
American Journal of Medical Genetics. Part A|January 13, 2016
Interstitial 6q25 microdeletion syndrome: ARID1B is the key geneLuisa Ronzoni, Francesco Tagliaferri, Arianna Tucci, et al.
Molecular Genetics and Metabolism|November 23, 2021
Comprehensive-targeted lipidomic analysis in Niemann-Pick C diseaseSara Boenzi, Giulio Catesini, Elisa Sacchetti, et al.
International Journal of Molecular Sciences|May 21, 2020
Vitamin D and Cardiovascular Risk: which Implications in Children?Silvia Savastio, Erica Pozzi, Francesco Tagliaferri, et al.
Orphanet Journal of Rare Diseases|July 19, 2022
Hepatic glycogen storage diseases type 0, VI and IX: description of an italian cohortFrancesco Tagliaferri, Miriam Massese, Luisa Russo, et al.
Nutrients|April 30, 2021
Healthy Lifestyle Intervention and Weight Loss Improve Cardiovascular Dysfunction in Children with ObesityGiulia Genoni, Veronica Menegon, Alice Monzani, et al.
Case Reports in Pediatrics|August 25, 2017
Late Onset Cobalamin Disorder and Hemolytic Uremic Syndrome: A Rare Cause of Nephrotic SyndromeGianluigi Ardissino, Michela Perrone, Francesca Tel, et al.
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