TAGLIAFERRI, FRANCESCO
TAGLIAFERRI, FRANCESCO
Dipartimento di Scienze Cliniche e di Comunità
Perceived severity and parental distress after positive expanded newborn screening: parent-clinician concordance and dyadic processes
2026 M. Bani, S. Russo, S. Gasperini, V. Crescitelli, F. Menni, F. Furlan, F. Tagliaferri, G. Cefalo, S. Paci, G. Banderali, P. Marchisio, A. Balduzzi, M.G. Strepparava
Vitamin-B12 status among the mother–infant dyad: an explorative overview in a single centre in Lombardy
2026 F. Furlan, F. Tagliaferri, S. Mariani, C. Berti, S. Salera, S. Lucchi, S. Ferraro, C. Cereda, G. Fiore, M. Tosi, A. Spano, F. Galandrini, C. Agostoni, E. Verduci, F. Menni
Late-onset severe axonal polyneuropathy in mut0 methylmalonic acidemia after liver-kidney transplantation: a genotype-informed case report
2026 M. Griffo, F. Magri, F. Furlan, E. Bernardi, F. Menni, F. Tagliaferri, S. Testa, D. Ronchi, S. Petrillo, F. Piemonte, D. Gagliardi, M. Parisi, S. Padelli, D. Velardo, N. Molitierno, S. Corti, G.P. Comi
Congenital Hyperinsulinism of a Large Italian Cohort: A Retrospective Study
2025 F. Tagliaferri, R. Iannuzzi, G. Canciani, S.M. Bernabei, C. Campana, S. Caviglia, B. Greco, F.R. Lepri, A. Novelli, M. Pizzoferro, M.C. Garganese, M. Spada, P. Francalanci, C. Dionisi-Vici, A. Maiorana
Prevalence and predictors of parental distress at the communication of positivity at newborn screening for metabolic diseases: An Italian longitudinal study
2024 M. Bani, S. Russo, S. Gasperini, V. Crescitelli, F. Menni, F. Furlan, F. Tagliaferri, G. Cefalo, S. Paci, G. Banderali, P. Marchisio, A. Biondi, M.G. Strepparava
Current understanding on pathogenesis and effective treatment of glycogen storage disease type Ib with empagliflozin: new insights coming from diabetes for its potential implications in other metabolic disorders
2023 A. Maiorana, F. Tagliaferri, C. Dionisi-Vici
Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI
2022 M. Massese, F. Tagliaferri, C. Dionisi-Vici, A. Maiorana
Hepatic glycogen storage diseases type 0, VI and IX: description of an italian cohort
2022 F. Tagliaferri, M. Massese, L. Russo, A. Commone, S. Gasperini, R. Pretese, C. Dionisi-Vici, A. Maiorana
A global overview of COVID-19 research in the pediatric field: Bibliometric review
2021 A. Monzani, F. Tagliaferri, S. Bellone, G. Genoni, I. Rabbone
Changing admission patterns in pediatric emergency departments during the covid-19 pandemic in italy were due to reductions in inappropriate accesses
2021 I. Rabbone, F. Tagliaferri, E. Carboni, B. Crotti, J. Ruggiero, A. Monzani, L. Bonetti, M. Soliani, S. Bellone, C. Cavalli, A.E. Scaramuzza
Management of a suspected case of 2019 novel coronavirus infection in a 4-year old child: A simulation scenario
2021 A. Monzani, G. Genoni, M. Binotti, F. Tagliaferri, I. Rabbone, P.L. Ingrassia
Comprehensive-targeted lipidomic analysis in Niemann-Pick C disease
2021 S. Boenzi, G. Catesini, E. Sacchetti, F. Tagliaferri, C. Dionisi-Vici, F. Deodato
A novel mutation in GCK gene: Beware of SGA child with diabetic mother
2021 F. Tagliaferri, C. Grosso, M. Balbo, G. Bracciolini, E. Bertelli, A. Secco, A. Salina, C. Aloi, M. Gallo, E. Felici
Healthy lifestyle intervention and weight loss improve cardiovascular dysfunction in children with obesity
2021 G. Genoni, V. Menegon, A. Monzani, F. Archero, F. Tagliaferri, V. Mancioppi, C. Peri, S. Bellone, F. Prodam
Vitamin D and cardiovascular risk: Which implications in children?
2020 S. Savastio, E. Pozzi, F. Tagliaferri, R. Degrandi, R. Cinquatti, I. Rabbone, G. Bona
Changing admission patterns in paediatric emergency departments during the COVID-19 pandemic
2020 A. Scaramuzza, F. Tagliaferri, L. Bonetti, M. Soliani, F. Morotti, S. Bellone, C. Cavalli, I. Rabbone
Vitamin D effects and endocrine diseases
2020 S. Savastio, R. Cinquatti, F. Tagliaferri, I. Rabbone, G. Bona
Late Onset Cobalamin Disorder and Hemolytic Uremic Syndrome: A Rare Cause of Nephrotic Syndrome
2017 G. Ardissino, M. Perrone, F. Tel, S. Testa, A. Morrone, I. Possenti, F. Tagliaferri, R. Dilena, F. Menni
Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene
2016 L. Ronzoni, F. Tagliaferri, A. Tucci, M. Baccarin, S. Esposito, D. Milani