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Neurology. Genetics|June 3, 2022
Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEEGanna Balagura, Julie Xian, Antonella Riva, et al.
Frontiers in Pediatrics|May 23, 2022
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter CohortChiara Po', Margherita Nosadini, Marialuisa Zedde, et al.
Neurology|February 12, 2016
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsyHannah Stamberger, Marina Nikanorova, Marjolein H Willemsen, et al.
Orphanet Journal of Rare Diseases|June 17, 2020
Mowat-Wilson syndrome: growth chartsIvan Ivanovski, Olivera Djuric, Serena Broccoli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 11, 2016
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patientsLivia Garavelli, Ivan Ivanovski, Stefano Giuseppe Caraffi, et al.
Neurology|December 5, 2020
Basal Ganglia Dysmorphism in Patients With Aicardi SyndromeSilvia Masnada, Anna Pichiecchio, Manuela Formica, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for careIvan Ivanovski, Olivera Djuric, Stefano Giuseppe Caraffi, et al.
Trials|August 20, 2016
Efficacy of a new technique - INtubate-RECruit-SURfactant-Extubate - "IN-REC-SUR-E" - in preterm neonates with respiratory distress syndrome: study protocol for a randomized controlled trialGiovanni Vento, Roberta Pastorino, Luca Boni, et al.
The Lancet. Respiratory Medicine|July 21, 2020
Lung recruitment before surfactant administration in extremely preterm neonates with respiratory distress syndrome (IN-REC-SUR-E): a randomised, unblinded, controlled trialGiovanni Vento, Maria Luisa Ventura, Roberta Pastorino, et al.
JAMA Network Open|September 25, 2024
Lung Recruitment Before Surfactant Administration in Extremely Preterm Neonates: 2-Year Follow-Up of a Randomized Clinical TrialFrancesca Gallini, Domenico Umberto De Rose, Roberta Iuliano, et al.
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