Prophylactic use of a probiotic in the prevention of colic, regurgitation, and functional constipation: a randomized clinical trial

F Indrio, A Di Mauro, G Riezzo, E Civardi, C Intini… - JAMA …, 2014 - jamanetwork.com
Importance Infantile colic, gastroesophageal reflux, and constipation are the most common
functional gastrointestinal disorders that lead to referral to a pediatrician during the first 6 …

Prevalence and characteristics of positional plagiocephaly in healthy full-term infants at 8–12 weeks of life

E Ballardini, M Sisti, N Basaglia, M Benedetto… - European journal of …, 2018 - Springer
Positional plagiocephaly (PP) denotes flattening of the skull that occurs frequently in healthy
infants. Aim of this study was to estimate the prevalence of positional plagiocephaly and to …

ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria

A Vetro, HN Nielsen, R Holm, RF Hevner, E Parrini… - Brain, 2021 - academic.oup.com
Constitutional heterozygous mutations of ATP1A2 and ATP1A3, encoding for two distinct
isoforms of the Na+/K+-ATPase (NKA) alpha-subunit, have been associated with familial …

[HTML][HTML] Prevention of neural tube defects in Europe: a public health failure

JK Morris, MC Addor, E Ballardini, I Barisic… - Frontiers in …, 2021 - frontiersin.org
Objective: Thirty years ago it was demonstrated that folic acid taken before pregnancy and in
early pregnancy reduced the risk of a neural tube defect (NTD). Despite Public Health …

Different pre-term formulas for different pre-term infants

S Fanaro, E Ballardini, V Vigi - Early human development, 2010 - Elsevier
Optimal nutrition is one of the most important aspects in the care of pre-term infants,
especially for the gestationally youngest ones. These infants should receive a supply of …

PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum

KM Johannesen, E Gardella, CE Gjerulfsen… - Neurology …, 2021 - AAN Enterprises
Background and Objectives Purine-rich element-binding protein A (PURA) gene encodes
Pur-α, a conserved protein essential for normal postnatal brain development. Recently, a …

Universal cranial ultrasound screening in preterm infants with gestational age 33-36 weeks. A retrospective analysis of 724 newborns

E Ballardini, A Tarocco, A Baldan, E Antoniazzi… - Pediatric …, 2014 - Elsevier
Background Cranial ultrasonography is a useful tool to detect intracranial lesions in
premature neonates at risk. Our primary aim was to determine the number of patients with …

[HTML][HTML] Survival of children with rare structural congenital anomalies: a multi-registry cohort study

A Coi, M Santoro, A Pierini, J Rankin… - Orphanet journal of rare …, 2022 - Springer
Background Congenital anomalies are the leading cause of perinatal, neonatal and infant
mortality in developed countries. Large long-term follow-up studies investigating survival …

Epidemiology of pierre‐robin sequence in Europe: a population‐based EUROCAT study

M Santoro, A Coi, I Barišić, A Pierini… - Paediatric and …, 2021 - Wiley Online Library
Abstract Background Pierre Robin sequence (PRS) is a rare congenital anomaly.
Respiratory disorders and feeding difficulties represent the main burden. Objective The aim …

Prevalence and associated factors for agenesis of corpus callosum in Emilia Romagna (1981–2015)

E Ballardini, P Marino, E Maietti, G Astolfi… - European journal of …, 2018 - Elsevier
Agenesis and hypoplasia of the corpus callosum (ACC and HCC) are heterogeneous group
with a large variation in published prevalence based on few population based studies. The …