| Concussion: A Global Perspective |
8 |
| Youth Exposure to Repetitive Head Impacts From Tackle Football and Long-term Neurologic Outcomes: A Review of the Literature, Knowledge Gaps and Future Directions, and Societal and Clinical Implications |
8 |
| Imaging Evidence of the Effect of Socio-Economic Status on Brain Structure and Development |
6 |
| Myoimaging in Congenital Myopathies |
6 |
| Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome |
5 |
| Stereotypic Movement Disorders |
5 |
| Movement Disorders and Neurometabolic Diseases |
5 |
| Autism in Children With Cerebral and Peripheral Visual Impairment: Fact or Artifact? |
4 |
| The Critical Role of the Central Autonomic Nervous System in Fetal-Neonatal Transition |
4 |
| Understanding Fetal Heart Rate Patterns That May Predict Antenatal and Intrapartum Neural Injury |
4 |
| Neuroprotection Strategies in Preterm Encephalopathy |
4 |
| Viral Infections and the Neonatal Brain |
4 |
| Perinatal Stroke |
4 |
| Socioeconomic Status and Pediatric Neurologic Disorders: Current Evidence |
4 |
| Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype |
3 |
| Global Burden of Pediatric Neurological Disorders |
3 |
| Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results |
3 |
| Pediatric Ataxia: Focus on Chronic Disorders |
3 |
| Myopathology of Congenital Myopathies: Bridging the Old and the New |
3 |
| The Twists of Pediatric Dystonia: Phenomenology, Classification, and Genetics |
3 |
| Neonatal Developmental and Epileptic Encephalopathies |
3 |
| Brain Injury During Transition in the Newborn With Congenital Heart Disease: Hazards of the Preoperative Period |
3 |
| Fetal Cerebrovascular Maturation: Effects of Hypoxia |
3 |
| Cerebral Visual Impairment and Clinical Assessment: The European Perspective |
3 |
| Profiling Children With Cerebral Visual Impairment Using Multiple Methods of Assessment to Aid in Differential Diagnosis |
2 |
| Promoting the Human Rights of Children With Neurologic Conditions |
2 |
| Circulatory Changes and Cerebral Blood Flow and Oxygenation During Transition in Newborns With Congenital Heart Disease |
2 |
| Diplopia With Dural Fibrotic Thickening |
2 |
| Hypothalamic Hamartoma With Infantile Spasms: Case Report With Surgical Treatment |
2 |
| Intracranial Calcifications in Young Children |
2 |
| Definition, Classification, and Epidemiology of Concussion |
2 |
| Diagnosis of Concussion in the Pediatric Emergency Department |
2 |
| Pathophysiology of Concussion |
2 |
| Neonatal Neurocritical Care: Providing Brain-Focused Care for All at Risk Neonates |
2 |
| The First Case of Riboflavin Transporter Deficiency insub-Saharan Africa |
2 |
| Anatomy, Physiology, and Clinical Syndromes of the Basal Ganglia: A Brief Review |
2 |
| Update on the Genetics of Congenital Myopathies |
2 |
| The Use of Muscle Ultrasound in the Diagnosis and Differential Diagnosis of Congenital Disorders of Muscle in the Age of Next Generation Genetics |
2 |
| Paroxysmal Dyskinesias |
2 |
| Pediatric latrogenic Movement Disorders |
1 |
| Management of Pediatric Movement Disorders: Present and Future |
1 |
| Therapeutic Aspects in Congenital Myopathies |
1 |
| Tremors: Essential Tremor and Beyond |
1 |
| Inherited and Acquired Choreas |
1 |
| Tic Disorders and PANDAS |
1 |
| Pregnancy and Delivery in Women With Congenital Myopathies |
1 |
| Signs and Symptoms in Congenital Myopathies |
1 |
| Infantile Epileptic Encephalopathy With Multiple Genetic Mutations: How Important are Variants of Undetermined Significance? |
1 |
| A Developmental Social Neuroscience Model for Understanding Pathways to Substance Use Disorders During Adolescence |
1 |
| Elevated Creatine Kinase in a 6-Year-Old Boy |
1 |
