关注
Francesco Tagliaferri
Francesco Tagliaferri
未知所在单位机构
没有经过验证的电子邮件地址
标题
引用次数
引用次数
年份
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
1002020
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
282022
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
282020
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
262016
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
162021
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
132021
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
122021
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
122021
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
102017
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
92023
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
82022
Vitamin D effects and endocrine diseases.
S Savastio, R Cinquatti, F Tagliaferri, I Rabbone, G Bona
Minerva Pediatrica 72 (4), 326-339, 2020
52020
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
12017
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
系统目前无法执行此操作,请稍后再试。
文章 1–17