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The authors describe the peculiar aspects of meningiomas in children on the basis of a large pool of data obtained from a review of 440 cases collected from the pertinent literature.
The authors provide a brief summary and perspective on some of the strengths and weaknesses of the cerebral palsy models, along with some historical context.
According to the authors, CD-ROM examination training is an efficient and cost-effective way to train neurologists and non-neurologists to perform structured neurologic exams in 1-year-old children.
The authors investigated the effects of prenatal overstimulation of the beta2-adrenergic receptor in dizygotic twins who were exposed to terbutaline as a gestational factor.
The authors present a patient with a delayed diagnosis at the age of 8 years when brain computed tomography was done because there was no first image from the age of 8 months when the disease began.
Can children's headache drawings aid the diagnosis of headache type and provide valuable insights into their experience of pain and the clinical course of their condition?
The aim of this study was to further define the clinical features of subcortical aphasia in children with deep brain infarcts and to define the sequelae associated with childhood strokes.
What, really, is ADHD? Is ADHD a collection of symptoms, or is it a disease entity? Who is qualified to diagnose, evaluate, and treat these symptoms or this condition?
Is it possible to provide a quantitative description of the organization and distribution of cerebral asymmetries in the brains of dyslexic individuals?
This article reviews the neuropathology of Rett syndrome and summarizes studies in the human and mouse brain that are beginning to reveal the disorder's pathoetiology.
Several articles have been written about the genetics of Rett syndrome. In this article, the authors summarize knowledge that is important for clinicians caring for these patients and their parents.
Do children with early global developmental delay demonstrate persistent and consistently poor performance across all developmental and functional domains?
The author presents the cases of three female patients with classic Rett syndrome, one still walking and two walking with support before the regression period.
In this study, the authors found that patients with cortical malformations frequently present intrapartum complications, which could lead to the misdiagnosis of hypoxic-ischemic encephalopathy.
The data support the findings that continuous spike-and-wave activity during slow-wave sleep results from secondary bilateral synchrony and that resective surgery can be effective in select patients.
Mission Statement:
Journal of Child Neurology
is an interdisciplinary peer-reviewed journal that publishes articles in the fields of child neurology, pediatric neurosurgery, pediatric neuroradiology, child psychiatry, pediatric neuropsychology, developmental and behavioral pediatrics, pediatric neuroscience and developmental neurobiology.
