Changing admission patterns in paediatric emergency departments during the COVID-19 pandemic A Scaramuzza, F Tagliaferri, L Bonetti, M Soliani, F Morotti, S Bellone, ... Archives of disease in childhood 105 (7), 704-706, 2020 | 100 | 2020 |
Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI M Massese, F Tagliaferri, C Dionisi-Vici, A Maiorana Orphanet Journal of Rare Diseases 17 (1), 241, 2022 | 28 | 2022 |
Vitamin D and cardiovascular risk: which implications in children? S Savastio, E Pozzi, F Tagliaferri, R Degrandi, R Cinquatti, I Rabbone, ... International journal of molecular sciences 21 (10), 3536, 2020 | 28 | 2020 |
Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene L Ronzoni, F Tagliaferri, A Tucci, M Baccarin, S Esposito, D Milani American Journal of Medical Genetics Part A 170 (5), 1257-1261, 2016 | 26 | 2016 |
Healthy lifestyle intervention and weight loss improve cardiovascular dysfunction in children with obesity G Genoni, V Menegon, A Monzani, F Archero, F Tagliaferri, V Mancioppi, ... Nutrients 13 (4), 1301, 2021 | 16 | 2021 |
A global overview of COVID-19 research in the pediatric field: bibliometric review A Monzani, F Tagliaferri, S Bellone, G Genoni, I Rabbone JMIR Pediatrics and Parenting 4 (3), e24791, 2021 | 13 | 2021 |
Comprehensive-targeted lipidomic analysis in Niemann-Pick C disease S Boenzi, G Catesini, E Sacchetti, F Tagliaferri, C Dionisi-Vici, F Deodato Molecular Genetics and Metabolism 134 (4), 337-343, 2021 | 12 | 2021 |
Changing admission patterns in pediatric emergency departments during the COVID-19 pandemic in Italy were due to reductions in inappropriate accesses I Rabbone, F Tagliaferri, E Carboni, B Crotti, J Ruggiero, A Monzani, ... Children 8 (11), 962, 2021 | 12 | 2021 |
Late onset cobalamin disorder and hemolytic uremic syndrome: a rare cause of nephrotic syndrome G Ardissino, M Perrone, F Tel, S Testa, A Morrone, I Possenti, F Tagliaferri, ... Case Reports in Pediatrics 2017 (1), 2794060, 2017 | 10 | 2017 |
Current understanding on pathogenesis and effective treatment of glycogen storage disease type Ib with empagliflozin: new insights coming from diabetes for its potential … A Maiorana, F Tagliaferri, C Dionisi-Vici Frontiers in Endocrinology 14, 1145111, 2023 | 9 | 2023 |
Hepatic glycogen storage diseases type 0, VI and IX: description of an italian cohort F Tagliaferri, M Massese, L Russo, A Commone, S Gasperini, R Pretese, ... Orphanet Journal of Rare Diseases 17 (1), 285, 2022 | 8 | 2022 |
Vitamin D effects and endocrine diseases. S Savastio, R Cinquatti, F Tagliaferri, I Rabbone, G Bona Minerva Pediatrica 72 (4), 326-339, 2020 | 5 | 2020 |
Case report late onset cobalamin disorder and hemolytic uremic syndrome: a rare cause of nephrotic syndrome G Ardissino, M Perrone, F Tel, S Testa, A Morrone, I Possenti, F Tagliaferri, ... Case Rep Pediatr, 1-4, 2017 | 1 | 2017 |
Congenital hyperinsulinism of a large Italian cohort: a retrospective study F Tagliaferri, R Iannuzzi, G Canciani, SM Bernabei, C Campana, ... Hormone Research in Paediatrics, 2024 | | 2024 |
Management of a suspected case of 2019 novel coronavirus infection in a 4‐year old child: A simulation scenario A Monzani, G Genoni, M Binotti, F Tagliaferri, I Rabbone, PL Ingrassia Journal of Paediatrics and Child Health 57 (5), 743, 2020 | | 2020 |
I difetti congeniti del metabolismo intracellulare della vitamina B12 I pazienti con difetti del metabolismo intracellulare della vitamina B12 presentano un fenotipo eterogeneo … F Tagliaferri, F Menni, F Bonarrigo, F Furlan | | |
I difetti congeniti del metabolismo intracellulare della vitamina B12 F Tagliaferri, F Menni, F Bonarrigo, F Furlan | | |