Published in Early Hum Dev on February 13, 2010
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Visual cortical function in very low birth weight infants without retinal or cerebral pathology. Invest Ophthalmol Vis Sci (2011) 0.86
Developmental synergy between thalamic structure and interhemispheric connectivity in the visual system of preterm infants. Neuroimage Clin (2015) 0.78
Impaired visual fixation at the age of 2 years in children born before the twenty-eighth week of gestation. Antecedents and correlates in the multicenter ELGAN study. Pediatr Neurol (2014) 0.76
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Local and global aspects of biological motion perception in children born at very low birth weight. Child Neuropsychol (2014) 0.75
A multicenter, randomized trial of prophylactic fluconazole in preterm neonates. N Engl J Med (2007) 4.72
Prevalence of the congenital long-QT syndrome. Circulation (2009) 4.32
Pediatric Outcome after Maternal Cancer Diagnosed during Pregnancy. N Engl J Med (2015) 3.37
Bovine lactoferrin supplementation for prevention of late-onset sepsis in very low-birth-weight neonates: a randomized trial. JAMA (2009) 3.34
Origin and timing of brain lesions in term infants with neonatal encephalopathy. Lancet (2003) 3.32
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. Brain (2007) 2.88
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy. Neuromuscul Disord (2010) 2.14
Short-term, long-term and paracrine effect of human umbilical cord-derived stem cells in lung injury prevention and repair in experimental bronchopulmonary dysplasia. Thorax (2012) 1.95
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. FASEB J (2007) 1.92
Emergence of resting state networks in the preterm human brain. Proc Natl Acad Sci U S A (2010) 1.86
The Hammersmith functional motor scale for children with spinal muscular atrophy: a scale to test ability and monitor progress in children with limited ambulation. Eur J Paediatr Neurol (2003) 1.64
Is hemiplegic cerebral palsy equivalent to amblyopia of the corticospinal system? Ann Neurol (2007) 1.60
Hand movements at 3 months predict later hemiplegia in term infants with neonatal cerebral infarction. Dev Med Child Neurol (2009) 1.56
Brain involvement in muscular dystrophies with defective dystroglycan glycosylation. Ann Neurol (2008) 1.52
Cramped synchronized general movements in preterm infants as an early marker for cerebral palsy. Arch Pediatr Adolesc Med (2002) 1.50
Do prebiotics reduce the number of fever episodes in healthy children in their first year of life: a randomised controlled trial. Br J Nutr (2011) 1.49
Developmental plasticity connects visual cortex to motoneurons after stroke. Ann Neurol (2010) 1.48
Prophylactic or early selective surfactant combined with nCPAP in very preterm infants. Pediatrics (2010) 1.47
Reliability of a novel, semi-quantitative scale for classification of structural brain magnetic resonance imaging in children with cerebral palsy. Dev Med Child Neurol (2014) 1.45
Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study. Dev Med Child Neurol (2010) 1.42
Ataluren treatment of patients with nonsense mutation dystrophinopathy. Muscle Nerve (2014) 1.41
The forward parachute reaction and independent walking in infants with brain lesions. Dev Med Child Neurol (2011) 1.39
Phenylbutyrate increases SMN gene expression in spinal muscular atrophy patients. Eur J Hum Genet (2005) 1.38
Vitamin K prophylaxis: leaving the old route for the new one? Acta Paediatr Suppl (2005) 1.38
Cognitive competence at the onset of West syndrome: correlation with EEG patterns and visual function. Dev Med Child Neurol (2005) 1.38
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy. PLoS One (2013) 1.34
Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy. Dev Med Child Neurol (2013) 1.30
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. Ann Neurol (2012) 1.29
Magnetic resonance imaging of white matter diseases of prematurity. Neuroradiology (2010) 1.26
Probabilistic diffusion tractography of the optic radiations and visual function in preterm infants at term equivalent age. Brain (2008) 1.26
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype. Nat Genet (2012) 1.25
Massage accelerates brain development and the maturation of visual function. J Neurosci (2009) 1.24
A critical review of functional assessment tools for upper limbs in Duchenne muscular dystrophy. Dev Med Child Neurol (2012) 1.20
A new approach for neurological evaluation of infants in resource-poor settings. Ann Trop Paediatr (2002) 1.17
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. Neurology (2012) 1.17
Multicity Italian study of congenital cytomegalovirus infection. Pediatr Infect Dis J (2006) 1.13
Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations. Neuromuscul Disord (2004) 1.10
The SafeBoosC phase II randomised clinical trial: a treatment guideline for targeted near-infrared-derived cerebral tissue oxygenation versus standard treatment in extremely preterm infants. Neonatology (2013) 1.10
Cognitive profile of disorders associated with dysregulation of the RAS/MAPK signaling cascade. Am J Med Genet A (2009) 1.10
The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children. Eur J Paediatr Neurol (2011) 1.09
Fracture prevalence in Duchenne muscular dystrophy. Dev Med Child Neurol (2002) 1.08
Magnetic resonance imaging assessment of brain maturation in preterm neonates with punctate white matter lesions. Neuroradiology (2006) 1.08
Immunogenicity, safety and tolerability of heptavalent pneumococcal conjugate vaccine administered at 3, 5 and 11 months post-natally to pre- and full-term infants. Vaccine (2005) 1.07
Dorsal and ventral stream sensitivity in normal development and hemiplegia. Neuroreport (2002) 1.07
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion. Hum Mutat (2009) 1.07
Galacto-oligosaccharides and long-chain fructo-oligosaccharides as prebiotics in infant formulas: a review. Acta Paediatr Suppl (2005) 1.06
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. Orphanet J Rare Dis (2013) 1.06
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance. AJNR Am J Neuroradiol (2003) 1.05
Neonatal cerebral infarction and neuromotor outcome at school age. Pediatrics (2004) 1.05
BPD: old and new problems. J Matern Fetal Neonatal Med (2011) 1.05
The pathophysiology of retinopathy of prematurity: an update of previous and recent knowledge. Acta Ophthalmol (2013) 1.05
CD20 expression has no prognostic role in Philadelphia-negative B-precursor acute lymphoblastic leukemia: new insights from the molecular study of minimal residual disease. Haematologica (2011) 1.05
Reduced occurrence of early atopic dermatitis because of immunoactive prebiotics among low-atopy-risk infants. J Allergy Clin Immunol (2010) 1.03
Magnetic resonance image correlates of hemiparesis after neonatal and childhood middle cerebral artery stroke. Pediatrics (2005) 1.03
SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR. Eur J Hum Genet (2010) 1.02
Differentiation and migration properties of human foetal umbilical cord perivascular cells: potential for lung repair. J Cell Mol Med (2011) 1.02
Bovine lactoferrin prevents invasive fungal infections in very low birth weight infants: a randomized controlled trial. Pediatrics (2011) 1.02
The effects of preterm infant massage on brain electrical activity. Dev Med Child Neurol (2011) 1.01
Apparent diffusion coefficient determination in normal fetal brain: a prenatal MR imaging study. AJNR Am J Neuroradiol (2003) 1.00
Thalamic atrophy in infants with PVL and cerebral visual impairment. Early Hum Dev (2006) 1.00
Spinal muscular atrophy. Orphanet J Rare Dis (2011) 1.00
Daily salbutamol in young patients with SMA type II. Neuromuscul Disord (2008) 1.00
Diffusion tensor imaging in preterm infants with punctate white matter lesions. Pediatr Res (2011) 0.99
Environmental enrichment decreases GABAergic inhibition and improves cognitive abilities, synaptic plasticity, and visual functions in a mouse model of Down syndrome. Front Cell Neurosci (2011) 0.99
Neonatal neuroimaging: going beyond the pictures. Early Hum Dev (2009) 0.99
Increase of faecal bifidobacteria due to dietary oligosaccharides induces a reduction of clinically relevant pathogen germs in the faeces of formula-fed preterm infants. Acta Paediatr Suppl (2005) 0.99
Water apparent diffusion coefficient and T2 changes in the acute stage of maple syrup urine disease: evidence of intramyelinic and vasogenic-interstitial edema. J Neuroimaging (2003) 0.98
Gynecologic cancers in pregnancy: guidelines of a second international consensus meeting. Int J Gynecol Cancer (2014) 0.98
Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutations. Arch Neurol (2011) 0.98
Severe hypertriglyceridemia in a newborn with monogenic lipoprotein lipase deficiency: an unconventional therapeutic approach with exchange transfusion. JIMD Rep (2013) 0.98
TREAT-NMD workshop: pattern recognition in genetic muscle diseases using muscle MRI: 25-26 February 2011, Rome, Italy. Neuromuscul Disord (2012) 0.98
Oral propranolol for retinopathy of prematurity: risks, safety concerns, and perspectives. J Pediatr (2013) 0.97
Natural history and long-term outcome of cardiac rhabdomyomas detected prenatally. Prenat Diagn (2004) 0.97
Rapid recovery of fat mass in small for gestational age preterm infants after term. PLoS One (2011) 0.97
Early neurodevelopmental assessment in Duchenne muscular dystrophy. Neuromuscul Disord (2013) 0.97
Attitudes and knowledge regarding influenza vaccination among hospital health workers caring for women and children. Vaccine (2007) 0.97
Longitudinal body composition data in exclusively breast-fed infants: a multicenter study. Obesity (Silver Spring) (2011) 0.97
Natural history of pulmonary function in collagen VI-related myopathies. Brain (2013) 0.97
Magnetic resonance imaging of muscle in nemaline myopathy. Neuromuscul Disord (2004) 0.96
Is term newborn body composition being achieved postnatally in preterm infants? Early Hum Dev (2009) 0.96
Mapping the differences in care for 5,000 spinal muscular atrophy patients, a survey of 24 national registries in North America, Australasia and Europe. J Neurol (2013) 0.96
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohort. Neuromuscul Disord (2013) 0.95
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies. BMC Med Genet (2010) 0.95