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Journal of Child Neurology|December 7, 2013
Reproducibility of detecting silent cerebral infarcts in pediatric sickle cell anemiaRobert I Liem, Jingxia Liu, Mae O Gordon, et al.Journal of Child Neurology|December 7, 2013
Predictors of response to vagus nerve stimulation in childhood-onset medically refractory epilepsyRavindra Arya, Hansel M Greiner, Amanda Lewis, et al.Journal of Child Neurology|December 23, 2011
Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2)Day M Burruss, Tim C Wood, Lesby Espinoza, et al.Journal of Child Neurology|December 23, 2011
Developmental delays in children with neurofibromatosis type 1Elizabeth A Soucy, Feng Gao, David H Gutmann, et al.Journal of Child Neurology|December 23, 2011
Effects of osmotic-release methylphenidate on height and weight in children with attention-deficit hyperactivity disorder (ADHD) following up to four years of treatmentTeodoro Durá-Travé, María Eugenia Yoldi-Petri, Fidel Gallinas-Victoriano, et al.Journal of Child Neurology|December 19, 2012
Giant axonal neuropathy caused by a novel compound heterozygous mutation in the gigaxonin geneMin Xu, Yu-wei Da, Lu Liu, et al.Journal of Child Neurology|May 15, 2012
Obstructive sleep apnea and primary snoring in children with epilepsySejal V Jain, Paul S Horn, Narong Simakajornboon, et al.Journal of Child Neurology|December 11, 2012
In utero diagnosis of PHACE syndrome by fetal magnetic resonance imaging (MRI)Daniel Martín Fernández-Mayoralas, Manuel Recio-Rodríguez, Ana Laura Fernández-Perrone, et al.Journal of Child Neurology|December 29, 2012
Fatal outcome in hemiconvulsion-hemiplegia syndromeHimali Jayakody, Charuta JoshiJournal of Child Neurology|December 29, 2012
Aspartylglucosaminuria: unusual neonatal presentation in Qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish familyThomas Opladen, Friedrich Ebinger, Johannes Zschocke, et al.Pageof 586